Conditions of your grant

These grant conditions, together with the grant award letter and the funding policies, set out the terms and conditions on which we make a grant to the host institution and grantholder.

 

Table of contents

  1. How these grant conditions apply
  2. Use of grant
  3. Grant staff
  4. Conduct of the grant activities
  5. Payment of grant
  6. Financial management of grant
  7. Consultancies, third party restrictions or arrangements
  8. Legal compliance, research practice and governance
  9. Trials supported by CRUK
  10. Non-CDD clinical trials
  11. Intellectual property
  12. Engagement, publicity and publication
  13. Transfer, variation, suspension and termination
  14. Liability, indemnity and insurance
  15. Governing law
  16. Definitions
  17. Schedule a. Special conditions for host institutions with no technology transfer agreement with CRUK or CRT
  18. Schedule b. Special conditions for policy & information targeted research projects

 

1. How these grant conditions apply

  1. Terms and Conditions: These Grant Conditions, together with the GAL and Funding Policies, set out the Terms and Conditions on which CRUK makes the Grant to the Host Institution and Grantholder. The Terms and Conditions may be amended at any time by CRUK and apply to the Grant as amended. To the extent of any inconsistency between these Grant Conditions and the GAL, the GAL prevails. Definitions are set out in section 16.

  2. Acceptance and activation: To receive the Grant, the Host Institution and Grantholder must accept the Grant in the manner set out in the GAL and shall each be deemed to have agreed to the Terms and Conditions. The Grantholder must activate the Grant within three (3) months of the Start Date.

  3. Adherence to Terms and Conditions: The Host Institution and Grantholder must ensure that all Research Personnel on CRUK grants comply with the Terms and Conditions.

 

2. Use of grant

  1. Use of Grant: The Grant may only be used for Grant Activities and only for costs incurred during the Grant Period, unless agreed in advance with CRUK.

  2. Eligible costs on Institute Core Grants: Institute Core Grants may be used to cover all reasonable operational and research costs, consistently with budgets approved from time-to-time with CRUK.

  3. Eligible costs on all other Grants: For all Grants that are not Institute Core Grants, the Grant may be used to cover Direct Costs and, where specified in the GAL, Directly Allocated Costs. Host Institutions based in the UK may not use the Grant to cover Indirect Costs. Host Institutions based outside the UK may use a portion of the Grant to cover Indirect Costs only if specified in the GAL.

  4. Salaries: Salary allocation may be used to fund salary and individual employment entitlements for Research Personnel funded by the Grant including, where applicable, annual leave. In the UK, this includes the employer’s national insurance contribution and an employer’s pension contribution, at a rate no higher than that used by the USS or NHS scheme, and outside the UK, at rates no higher than contributions required by statute or available to other employees of the Host Institution at an equivalent level. Salary allocation must not be used:

    1. to offset any prior underfunding of a pension or superannuation scheme;

    2. to pay any bonus or merit awards;

    3. to cover any recruitment costs, including any student recruitment costs.

  5. Studentship costs: Where the Grant funds a studentship, the Grant may be used to cover:

    1. a stipend set by CRUK (which must be paid to the student for the duration of the studentship);

    2. the student’s running expenses;

    3. university fees at a rate no higher than the home/EU fees applied to students funded by UK Research Councils unless otherwise specified in the GAL; and

    4. college fees for the University of Oxford and University of Cambridge;

    5. only those studentships approved as part of the original Grant application (ie. running expense and salary allocations may not be used to fund additional studentships).

  6. Parental or other long-term leave: Where the Grant funds an individual’s salary, and that individual takes parental leave or other long-term leave, the Grantholder must notify CRUK. The Host Institution may only use the salary allocation for that individual as cover for the vacant position and may not use it to pay the individual’s leave entitlements. The Host Institution must bear the costs of the individual’s parental or other long-term leave consistent with its own employment policies regardless of the fact that the employee’s salary is paid from the Grant.

  7. Research carried out in the NHS: Grantholders carrying out research in the NHS must ensure that all costs are attributed according to the AcoRD (Attributing the costs of heath & social care Research & Development) Guidelines, or equivalent.

  8. Patient and volunteer costs: The Grant may be used to pay patient or volunteer travel and subsistence costs only as specified in the GAL. CRUK will not pay for participation costs, including prizes or gift vouchers, for patients and volunteers.

  9. Equipment: Where the Grant includes funds for Equipment, the Host Institution must:

    1. only use those funds to purchase the items specified in the GAL and ensure they are used primarily for the Grant Activities during the Grant Period;

    2. have clearly defined procurement procedures and comply with them in procuring the Equipment funded by the Grant. The Grant may not be used to cover any taxes payable due to the Host Institution’s failure to claim relief on qualifying Equipment;

    3. repair or replace Equipment at the Host Institution’s cost if it is lost, damaged or destroyed during the Grant Period.

  10. Ownership of Equipment: Any Equipment purchased using the Grant shall be owned by the Host Institution. Where the Host Institution is not a registered charity, at the end of the Grant Period, CRUK may request that the Host Institution pay CRUK an amount equal to the market value of the Equipment at the End Date assessed by an independent valuation expert approved by CRUK.

  11. Access charges: CRUK will not pay access charges for use of Equipment funded by any CRUK grant.

  12. Transfer between budget allocations (virement): The Host Institution may freely transfer funds between the salary and running expenses budget allocations set out in the GAL provided that:

    1. transfers are not made:

      • from any amount allocated for the Grantholder’s or Principal Investigator’s salary;

      • to or from any amount allocated for Equipment, or

      • from the salary of any post unfilled for six (6) months or more;

    2. transferred funds are only used to cover:

      • the Direct Research Costs of the Grant Activities; or

      • costs incurred by Research Personnel travelling (via standard class) and attending conferences related to the Grant Activities; and

    3. all transfers between budget allocations are declared at each financial reconciliation.

 

3. Grant staff

  1. Advertisements for grant staff: All advertisements for staff funded by the Grant must indicate that the research is funded by CRUK. The Host Institution is responsible for advertising posts and recruitment costs.

  2. CRUK not an employer: CRUK does not employ the Grantholder or Research Personnel. The Host Institution must ensure that any necessary contracts of employment are issued in relation to the Grant. CRUK accepts no responsibility for any claims for which the Host Institution, Research Personnel or any Institution may be liable as an employer or otherwise.

  3. Grantholders and other Research Personnel on clinical Grants: The Host Institution must ensure all clinical Research Personnel hold honorary NHS clinical contracts (or equivalent, if based outside the UK) or honorary university contracts at the appropriate level. They must also have necessary professional registration, occupational health clearance and professional indemnity insurance. CRUK accepts no liability for any claim arising out of matters relating to fitness to practice.

  4. Non-research responsibilities of fellowship holders: Unless otherwise agreed with CRUK, Host Institutions should ensure that CRUK fellows are able to dedicate at least 80 per cent of their time to the Grant Activities that are the subject of their fellowship Grant. Any other employment responsibilities assigned to a CRUK fellow should be limited to a maximum of 20 per cent of their time.

  5. Students: Where the Grant funds a studentship, the following provisions apply:

    1. the Grantholder must notify CRUK of the student’s name, email address, project title and start date within thirty (30) days of the Start Date;

    2. if agreed with their supervisor, students may spend up to 10 per cent of their time on teaching duties;

    3. where the Host Institution is part of a CRUK Centre, the Host Institution must ensure that all students at that Centre have access to the same training and benefits irrespective of whether they are funded through the Centre;

    4. on completion of the studentship, the Grantholder must provide CRUK with a copy of the student’s thesis title, abstract and outcome of the viva voce examination. If a student fails to complete their PhD, the Grantholder must inform CRUK of the reason;

    5. students and supervisors must complete a final year report at the end of the studentship;

    6. the Grantholder must advise CRUK of the student’s first post after completion of their PhD and, if the first post is 12 months or less, the student’s second post. (Email students@cancer.org.uk).

  6. Studentships on grants: Unless otherwise agreed with CRUK, students on Grants must be fully funded by the Grant and must be recruited at a time that allows them to complete their studentship during the Grant Period.

 

4. Conduct of the grant activities

  1. Grant Period: The Grantholder must use their best endeavours to ensure the Grant Activities are completed within the Grant Period. Any delay to the Start Date must be approved by CRUK.

  2. Training, resources, facilities and risk: The Host Institution must ensure that:

    1. all Research Personnel receive training appropriate to their duties;

    2. adequate resources, premises and facilities are provided to support the Grant Activities and their achievement within the timeframe described in the GAL;

    3. all equipment used for the Grant Activities (including, but not limited to, Equipment as defined in section 16) is fully maintained and insured throughout its useful life, and safe; and

    4. it identifies and safely manages any risks which could affect the health of the Grantholder, other Research Personnel and any other person who could be affected by the Grant Activities.

  3. Cell line authentication: Grantholders and Research Personnel using cell cultures must incorporate a best practice cell line authentication protocol into their experimental framework, following the ‘Guidelines for use of cell lines in biomedical research’ as set out by Geraghty et al (British Journal of Cancer (2014) Sep 9; 111(6):1021-46).

  4. Human Biological Samples: Where the Grant Activities include the removal, use or storage of Human Biological Samples, the Grantholder must:

    1. comply with applicable legislation, standards and codes of practice (see also MRC guidance note, ‘Human Tissue and Biological Samples for Use in Medical Research’ (2014));

    2. where possible, actively seek to establish sample collections that will be made available to and useful for the wider cancer research community, including by obtaining appropriate patient consents, and collecting data in a form that may be used by other researchers; and

    3. publicise the purpose, the nature of the content and other appropriate details of any new collections on the UKCRC Tissue Directory (and any other directories indicated by Cancer Research UK) and establish mechanisms to manage access by other researchers to those collections.

  5. Use of animals: Research Personnel may not carry out any animal research using the Grant unless specifically set out in the Grant application. In addition to its obligations under section 8.1 to comply with all applicable laws, the Host Institution must ensure that research involving animals gives due consideration to the refinement, reduction and replacement of animals in research and adhere to:

    1. the principles in the NC3Rs ‘Responsibility in the Use of Animals in Bioscience Research’ available on the NC3Rs website);

    2. the ‘Guidelines for the Welfare and Use of Animals in Cancer Research’ as set out in Workman et al (2010) (British Journal of Cancer 102, 1555-1577); and

    3. the ARRIVE Guidelines (Animal Research: Reporting of In Vivo Experiments) (also available on the NC3Rs website).

  6. New treatments: The CDD must be notified of any potential new treatment arising from the Grant.

  7. Scientific milestone reports: Where a Grant is made in more than one instalment, the Grantholder must submit a scientific milestone report in a form and at a time determined by CRUK. Subsequent instalments will only be made if CRUK deems that Grant Activities have progressed satisfactorily.

  8. Final reports: Any final report required by the GAL must be submitted no later than three (3) months after the End Date or such other date specified in the GAL.

  9. Additional monitoring obligations: Where the Host Institution is based outside the UK or is not a registered charity, it must provide CRUK with information, at least annually, to enable CRUK to effectively monitor the progress of the Grant Activities consistently with its monitoring and oversight obligations under UK charity law. Such information will include interim and final financial reports with itemised costs and expenses to which the Grant has been applied.

 

5. Payment of grant

  1. Grant is total amount payable: The Grant is the total aggregate amount payable by CRUK to the Host Institution and is inclusive of all sums (including, among others, all taxes, currency conversions, transfer costs and other charges) that may apply. If any of those sums do apply, they will be borne by the Host Institution. The Host Institution is responsible for any expenditure on Grant Activities in excess of the Grant amount stipulated in the GAL.

  2. Indexation: Once CRUK has established the amount of the Grant to be paid in the first year, a fixed indexation rate, determined by CRUK in its sole discretion, will be applied to all subsequent years of the award for salaries and running expenses.

  3. Payments: Unless the GAL or Special Conditions provide otherwise, CRUK will generally pay Grant funds quarterly in arrears in pounds sterling to the account nominated by the Host Institution. CRUK will not pay the final quarter of the Grant until it has processed the final reconciliation submitted under section 6.2 and the Grantholder has submitted any final report required by the GAL.

  4. Joint awards: Where two or more institutions hold a Grant jointly, CRUK may select one institution as the designated Host Institution. The designated Host Institution only shall receive the Grant payments and must transfer appropriate funds to the other institution(s) without undue delay.

 

6. Financial management of grant

  1. Financial management: The Host Institution must ensure proper financial management of the Grant and accountability for the use of public funds, including by keeping proper books and records of Grant expenditure, and by applying its usual arrangements for monitoring and preventing fraud bribery and any other corrupt practices. The Host Institution must account for all income and expenditure related to the Grant through a separate cost centre or, if it does not use cost centres, it must keep the Grant in a separate bank account used exclusively for the Grant funds.

  2. Reconciliation of Grant: The Host Institution must submit a final reconciliation at the end of the Grant and, where the Grant Period exceeds three (3) years, an interim reconciliation at three (3) year intervals from the Start Date. CRUK will process reconciliations as it reasonably sees fit. CRUK may recover any unspent Grant funds or ineligible costs and may offset any amounts owed to CRUK against any other sums (including any grant payments) owed to the Host Institution. The Host Institution must submit any Equipment claims within the relevant year specified in the GAL and provide copies of relevant invoices along with the claim.

  3. Additional reconciliation provisions for Host Institutions based outside the UK: Unless otherwise agreed with CRUK, reconciliations must be submitted in pounds sterling. Where the Host Institution has incurred costs in a currency other than pounds sterling, in submitting its reconciliation, the Host Institution must apply the historical exchange rate quoted on www.xe.com for the date the GAL was issued (or any alternative third party exchange rate calculator or date notified by Cancer Research UK before processing the reconciliation). CRUK is not liable for any losses incurred by the Host Institution through currency fluctuations. Any actual gains made by the Host Institution as a result of currency fluctuations must be used for the purposes of the Grant Activities or paid to CRUK following the financial reconciliation of the Grant.

  4. Audits and site visits: CRUK may seek confirmation from the Host Institution or the Host Institution’s external auditors that the Grant has been used in accordance with the Terms and Conditions. CRUK (or its agents) may also conduct its own audit of the Grant at any time and the Host Institution shall co-operate fully in that regard, including by allowing CRUK to inspect all books, records and facilities related to the Grant, by providing copies of all relevant books and records on request, and by procuring that any subcontractors provide that assistance as well.

 

7. Consultancies, third party restrictions or arrangements

  1. Host Institution’s responsibility to manage third party arrangements: The Host Institution shall not enter into, or permit Research Personnel to enter into, consultancies, third party restrictions or arrangements which may give rise to conflicts of interest or affect the Grant Activities or Funded Intellectual Property without the prior agreement of CRUK.

  2. Conflicts of interest: The Host Institution and Grantholder must avoid any conflicts of interest in relation to the Grant Activities and notify CRUK if any conflict of interest arises.

     

8. Legal compliance, research practice and governance

  1. Applicable laws and regulations: The Host Institution must ensure that the Grant Activities are carried out in accordance with all applicable legal, health and safety, ethical and regulatory requirements (including any clinical trials registration and Clinical Practice Standards), and that all licences and approvals necessary for the Grant Activities are obtained.

  2. Public benefit: The Host Institution must ensure that CRUK is not put at risk of breaching UK charity laws or regulations because of any relationship between a third party and the Host Institution, the Grantholder or Research Personnel. The Host Institution must ensure that the Grant, the Grant Activities and the useful Results are applied for public benefit, and that any private benefit is only incidental and is not excessive.

  3. Research integrity: The Host Institution and Grantholder must conduct the Grant Activities in accordance with the highest standards of research integrity including, where applicable, in accordance with Universities UK’s ‘Concordat to Support Research Integrity’. The Host Institution must also:

    1. make reasonable efforts to mitigate the risk of scientific misconduct occurring consistently with CRUK’s ‘Guidelines for Scientific Conduct’;

    2. have in place formal written procedures for the handling of allegations of research misconduct and make those procedures available on to CRUK on request;

    3. notify CRUK at the earliest opportunity of any allegations of research misconduct connected in any way with the Grant or Grant Activities, as well as the progress and outcome of any ensuing investigation into the misconduct.

      CRUK also reserves the right for it, or its agents, to investigate any aspect of fraud or misconduct itself and the Host Institution and Grantholder shall provide assistance and information to CRUK for that purpose.

  4. CRUK Funding Policies and research practices: Host Institutions and Grantholders must comply with all CRUK Funding Policies, including without limitation, CRUK’s policies on Data Sharing & Preservation, Open Access, and ResearchFish. Host Institutions must also follow appropriate principles, standards and practices for the proper management of research including, in the UK, the principles set out in the ‘Concordat to Support the Career Development of Researchers (2008)’ (as amended).

  5. Change in status: The Host Institution and Grantholder must notify CRUK if there is any change their status, or the status of any Research Personnel, that may affect their eligibility to hold the Grant.

  6. Freedom of information requests: If the Host Institution receives a freedom of information request in relation to any part of the Grant or Grant Activities, it must notify and consult with CRUK on the response to the request.

  7. CRUK’s right to disclose information: CRUK may disclose information regarding the Grant application, the Grant or the Grant Activities to its group and associated companies, relevant regulatory authorities, higher education funding councils and other agencies administering governmental funding.

     

9. Trials supported by CRUK

  1. NIHR CRN Support: UK-based trials or UK-based arms of trials funded by CRUK (or, subject to NIHR requirements, trials endorsed by CRUK) can be included in the NIHR CRN portfolio through the automatically eligible route to access NIHR CRN support. The Grantholder must ensure that up-to-date trial information, including recruitment data, is submitted monthly through the designated accrual data contact.

  2. Registration of trials: The Grantholder must register any CRUK-funded or endorsed trial on a recognised trials registry such as the ISRCTN registry, the EU Clinical Trials Register (EudraCT) or the ClinicalTrials.gov register.

  3. CRUK trials database: Grantholders and Research Personnel conducting trials and/or studies will assist the CRUK Patient Information Team by:

    1. including the URL for CRUK’s clinical trials database (cruk.org/trials) on the patient information sheet. (Including the CRUK logo is also strongly encouraged);

    2. providing CRUK with the study protocol and patient information sheet;

    3. assisting CRUK to draft a lay summary of the trial (and findings, as and when Results are available) for inclusion on CRUK’s online clinical trials database.

  4. Collection of NHS numbers: The NHS number (or equivalent) must be recorded for all patients entering late phase clinical trials or feasibility studies supported by CRUK. The collection of NHS numbers is strongly encouraged in trials of healthy volunteers and any other CRUK-supported study where long-term follow-up is likely.

     

10. Non-CDD clinical trials

  1. Trials supported by commercial entities: Where a Non-CDD Clinical Trial is supported in any way by a commercial entity to whom Host Institution intends to grant rights to the Non-CDD Clinical Trial Results of the trial, the Host Institution must:

    1. notify CRUK as soon of practicable of the commercial relationship and any monetary consideration it receives from the commercial entity;

    2. regularly consult with CRUK (or, at CRUK’s request, with CRT) and seek to agree with the commercial entity any arrangements that CRUK (or CRT) suggests;

    3. enter into a fair and appropriate revenue sharing agreement with CRUK (or, at CRUK’s request, CRT) in relation to any monetary consideration received by the Host Institution for the rights to the Non-CDD Clinical Trial Results (which shall at least reimburse CRUK for the funding it provided in support of the trial).

       

11. Intellectual property

  1. Funded Intellectual Property: Funded Intellectual Property shall, in the first instance, vest in the Host Institution. The Host Institution shall ensure that the contracts of employment or other terms of engagement of its Research Personnel provide for automatic and immediate vesting in the Host Institution of Funded Intellectual Property. The Host Institution and its Research Personnel shall co-operate fully with CRUK and CRT in all matters relating to Funded Intellectual Property.

  2. Technology Transfer Agreements: Following receipt of a request by CRT or CRUK, the Host Institution will negotiate and enter into a TTA with CRT in relation to Funded Intellectual Property. In the event that there is a TTA in place between CRT and the Host Institution, the terms of such TTA shall supersede Schedule A from the date such agreement becomes effective. In the event that there is no TTA in place the Host Institution agrees to the Special Conditions in Schedule A.

  3. CDD Projects: Where the Grant Activities involve a CDD Project, the Host Institution will enter into a CDD Agreement. Until the CDD Agreement comes into effect, any Results generated by the Host Institution will be Funded Intellectual Property subject to this section 11 and the Special Conditions in Schedule A. Results arising from CDD Projects are confidential and should not be disclosed without the prior consent of CRUK.

     

12. Engagement, publicity and publication

  1. Responsibility to act as peer reviewer when requested by CRUK: The Grantholder and Research Personnel will respond positively and punctually to requests from CRUK to peer review CRUK grant applications.

  2. Participation in fundraising and publicity: CRUK may use data or other material from research it funds for fundraising or publicity purposes. The Grantholder and CRUK-funded Research Personnel will promote CRUK and its charitable aims by complying with all reasonable requests from CRUK to attend or speak at events, and provide help with images and copy for CRUK publications. The Host Institution will also co-operate in relation to publicity, research engagement and fundraising activity for CRUK. Where CRUK is the largest or most significant contributing funder of the research, it reserves the right to lead on publicity.

  3. Press: The Grantholder and Host Institution must contact the CRUK Press Office before making any public announcements regarding the Grant Activities, especially in the case of clinical trials. When speaking publicly, the Grantholder and Research Personnel should identify themselves as ‘CRUK-funded researchers’ but be clear that they are not speaking on behalf of the Charity.

  4. Branding, Communications and Engagement: Grantholders and Host Institutions must comply with any guidelines for branding, communications and engagement that CRUK may issue from time to time. Host Institutions should ensure that prominent CRUK branding is displayed in CRUK-funded Centres, ECMCs, Core Funded Institutes and any other place where a major programme of work is funded by CRUK.

  5. Acknowledgment of CRUK support: Grantholders must acknowledge CRUK’s support (and, where possible, include CRUK’s logo) in all publications, oral or written reports, posters, presentations and information posted on websites that relate to the Grant Activities or Results or Non-CDD Clinical Trial Results.

  6. Publishable abstracts: At the time of application, grant applicants must provide publishable information about the proposed research and contact information which, if the application is successful, may be published on CRUK’s website.

  7. Dissemination of findings: The Grantholder must publish or otherwise disseminate appropriately verified Results to the broader scientific community as soon as possible, although CRUK or the Host Institution may delay dissemination for a reasonable period in order to protect intellectual property (including through compliance with a TTA, or section 19 of the Special Conditions in Schedule A, as applicable).

  8. Requirements for publications: Grantholders must:

    1. provide CRUK with details of all publications arising from the Grant Activities at the time of submission for publication via the online manuscript submission form on CRUK’s website;

    2. acknowledge CRUK’s support in the format ‘This work was supported by Cancer Research UK [C ref./A ref.]’) and, for trial results, the CRUK trial number; and

    3. within 6 months of any publication in a peer reviewed journal, ensure that a copy of each paper funded wholly or partly by the Grant is deposited in Europe PubMed Central.

  9. CDD Projects: Subject to any CDD Agreement, Grantholders must not publish or disclose any work relating to a CDD Project without the CDD’s prior consent. Grantholders should also consult the CDD as to who should be included in the list of authors. Media disclosures regarding CDD Projects and trials must be discussed in advance with the Director of the CDD (as well as the CRUK Press Office as per section 12.3).

     

13. Transfer, viariation, suspension and termination

  1. Transfer of Grant: The Grantholder may transfer the Grant to another institution only with the consent of the Host Institution, the new institution and CRUK, and only if the new institution agrees to be bound by the Terms and Conditions as the new Host Institution. CRUK may require that Equipment funded by the Grant is transferred with the Grantholder.

  2. Variation: CRUK may amend these Grant Conditions, its Funding Policies and the terms of the GAL at any time. It will publish any changes to the Grant Conditions and Funding Policies on its website. Once published, any changes apply to the Grant.

  3. Early termination of Grant Activities: In the event the Grant Activities are terminated early, the Grantholder and Host Institution must promptly notify CRUK. The Host Institution must then submit a reconciliation in accordance with section 6.2.

  4. Suspension or Termination of Grant: CRUK may suspend or terminate the Grant at any time and for any reason. So far as reasonably practicable, CRUK shall endeavour to give the Grantholder and Host Institution at least 30 days’ prior notice, but shall be entitled to terminate immediately.

  5. Survival of terms: The following sections of these Grant Conditions continue to apply after the End Date: sections 2.1, 2.10, 3.2, 3.5, 4.2.3, 4.2.4, 4.4, 4.5, 4.6, 4.8, 4.9, 6, 7, 8, 9.3, 10.1, 11, 12, 14 and 15.

     

14. Liability, indemnity and insurance

  1. Liability: CRUK relies entirely on the Host Institution to ensure that Grant Activities are carried out in accordance with best practice to avoid damage, loss or injury to persons or property. The Host Institution must also ensure Results are appropriately validated before publication. CRUK accepts no responsibility for costs incurred other than those specifically set out in the GAL, nor any liability for any accident, injury or loss sustained by any person in connection with the Grant Activities or publication of Results.

  2. Indemnity: In accepting the Grant, the Host Institution agrees to indemnify CRUK against any costs, claims or liabilities (including legal costs) suffered or incurred by CRUK as a result of any action, claim or complaint brought against CRUK in connection with or arising from any Grant Activities or Research Personnel or the accuracy or application of the Results.

  3. Insurance: The Host Institution must ensure that it (and, so far as is relevant, the Research Personnel and Institutions) hold appropriate insurances for professional indemnity, public liability and employer’s liability during the Grant Period and for a period of six (6) years after and during any commercialisation of the Results.

  4. No-fault compensation for clinical trials: The Host Institution of any CRUK-funded or CRUK-supported trial must provide a no-fault compensation scheme for participants. CRUK will not provide indemnity cover for or accept any liability for harm to participants where CRUK is not the trial sponsor.

     

15. Governing law

  1. The Terms and Conditions are governed by the laws of England and Wales. The Host Institution and Grantholder irrevocably and unconditionally submit to the exclusive jurisdiction of the English courts in respect of disputes arising out of or in connection with the Terms and Conditions.

     

16. Definitions

ARRIVE Guidelines

Animal Research: Reporting of In Vivo Experiments Guidelines published by the UK National Centre for the Replacement, Refinement & Reduction of Animals in Research.

CDD

CRUK’s Centre for Drug Development.

CDD Agreement

Agreement between CRUK and the Host Institution in relation to a CDD Project. The CDD Agreement will set out, among other things, the studies to be undertaken by the Host Institution in relation to the CDD Project and the ownership of the results of such studies.

CDD Projects

A phase I/II clinical trial which: (i) is carried out on a novel agent or therapy approved by CRUK’s New Agents Committee; (ii) managed through CRUK’s Centre for Drug Development; (iii) sponsored by CRUK; and (iv) may be supported partly by a CRUK Grant.

Centre

The network of cancer-research activity supported by grants described as CRUK centres grants.

Clinical Practice Standards

Guidance relating to medicines and clinical trials in force in the jurisdiction in which that Team Member is carrying out Activities or is registered, including the ICH Harmonised Tripartite Guideline for Good Clinical Practice (CPMP/ICH/135/95) and the World Medical Association Declaration of Helsinki entitled ‘Ethical Principles for Medical Research Involving Human Subjects’ (2008 version), in each case, as amended from time to time. For the avoidance of doubt, in the UK this includes the MRC Guidelines for Good Clinical Practice.

CRT

Cancer Research Technology Limited, a company registered in England & Wales No: 1626049 whose registered address is Angel Building, 407 St John Street, London EC1V 4AD and wholly owned subsidiary of CRUK.

CRUK

Cancer Research UK, a registered charity in England and Wales (1089464), in Scotland (SC041666) and in the Isle of Man (1103) and a company limited by guarantee registered in England & Wales No. 4325234 and the Isle of Man No. 5713F, whose registered address is Angel Building, 407 St John Street, London EC1V 4AD.

CRUK Core Funded Institute

Each of the following: the CRUK Beatson Institute, the CRUK Cambridge Institute, the CRUK Manchester Institute, the CRUK/MRC Oxford Institute for Radiation Oncology and the Francis Crick Institute.

Directly Allocated Costs

Costs of resources used by a project that are shared by other activities and based on estimates rather than actual costs (e.g. principal and co-investigator costs, estates costs).

Direct Costs

The costs explicitly identifiable as arising from the conduct of a project. In determining whether a cost is a Direct Cost, the Host Institution must follow any Costs Guidance issued by CRUK from time to time.

ECMC

CRUK-funded Experimental Cancer Medicine Centre.

End Date

The date that is the number of months from the Start Date that is equivalent to the duration of the award set out in the GAL, or such earlier date that the Grant is terminated.

Equipment

The equipment required to conduct the Grant Activities which costs £5,000 or more.

Funded Intellectual Property

All Results other than: (i) Results of CDD Projects (in respect of which a CDD Agreement has been completed); and (ii) Non-CDD Clinical Trial Results.

Funded Materials

Biological and chemical materials comprised in Funded Intellectual Property.

Funding Policies

The funding policy statements published on CRUK’s website, as updated from time to time.

GAL

The grant award letter from CRUK containing the details, and offer, of the Grant.

Grant

The funding made pursuant to and described in the GAL.

Grant Activities

The research and investigation funded by the Grant as described in the GAL.

Grant Conditions

The conditions set out in this document including, if applicable, the Special Conditions in Schedules A and B.

Grant Period

The period between the Start Date and End Date.

Grantholder

The lead applicant, any joint applicant as specified in the GAL and, for Institute Core Awards, CRUK-funded group leaders.

Host Institution

The university, research institution or other entity at which some or all of the Grant Activities will be carried out, as named in the GAL.

Human Biological Samples

Tissue, blood and other biological samples taken from humans.

Institutions

Any university, research institution or other entity at which some or all of the Grant Activities will be carried out other than the Host Institution.

Indirect Costs

Non-specific costs charged across all projects that are based on estimates (eg. human resources, finance, library and departmental services).

Institute Core Grants

A Grant issued to a CRUK Core Funded Institute that is described in the GAL as a ‘core’ award.

NIHR CRN Portfolio

A database of the clinical research studies that are supported by the National Institute of Health Research Clinical Research Network in England.

Non-CDD Clinical Trial

A clinical trial that is not a CDD Project or sponsored by CRUK, but which is supported directly or indirectly by a Grant.

Non-CDD Clinical Trial Results

All Results arising from a Non-CDD Clinical Trial, other than Human Biological Samples.

P&I

CRUK’s Policy & Information directorate.

Research Personnel

The Grantholder and any person working on the Grant Activities under his/her supervision, including (as applicable), any co-investigator or collaborator, sponsor, supervisor, consultant or sub-contractor.

Results

All inventions, discoveries, materials (including biological and chemical materials), technologies, products, data, algorithms, software, patents, databases, copyright, other intellectual property and know-how arising from Grant Activities.

Special Conditions

The Special Conditions notified to the Grantholder and Host Institution as applicable to the Grant in light of the nature of the funding scheme and Grant Activities and:

  • if there is no TTA between the Host Institution and CRUK or CRT, the Special Conditions in Schedule A to these Grant Conditions; and

  • if the grant is identified in the GAL as a P&I targeted research project, the Special Conditions in Schedule B to these Grant Conditions.

Start Date

The date indicated in the GAL, or otherwise agreed with CRUK, on which the Grant Activities commence.

Studentship

A Grant or part of a Grant pertaining to the funding of PhD students.

TTA

Technology Transfer Agreement being, unless CRT determines otherwise, a framework agreement governing the management and exploitation of Results as well as results of all other research funded by Cancer Research UK at the Host Institution from time to time.

Terms and Conditions

Together, the Grant Conditions, GAL and Funding Policies.

 

 

Schedule A. Special conditions for host institutions with no technology transfer agreement with CRUK or CRT

  1. Non-commercial research: The Host Institution grants CRUK the non-exclusive right itself, or by granting to recipients of CRUK funding the right, to use Funded Intellectual Property for the purposes of non-commercial research whether alone or in collaboration with third parties and whether sponsored or funded, in whole or in part, by any third party including any commercial entity.

  2. Identifying Funded Intellectual Property: The Host Institution shall allow CRT to visit its premises and to liaise freely and at will with its Research Personnel for the purpose of identifying Funded Intellectual Property. In addition, promptly following the identification by the Host Institution (or its agent) of any Funded Intellectual Property which appears to the Host Institution to have potential to be translated to deliver patient benefit or which can otherwise be exploited commercially, the Host Institution shall notify CRT in writing giving full details of such Funded Intellectual Property.

  3. Prior notification of CRT: CRT must be notified in good time (and in any event at least thirty (30) days) before either presentation or publication of any Results, whether patentable or not, which appear to be suitable for commercial exploitation or that are otherwise worthy of protection. At CRT’s request, the dissemination of Results will be delayed to enable the protection of Funded Intellectual Property.

  4. Protection of Funded Intellectual Property: The Host Institution shall take the steps necessary to protect Funded Intellectual Property as is reasonable to do so with regard to commercial considerations, however it shall not make (or permit others to make) any application for registered protection (including a patent) in connection with Funded Intellectual Property without the prior written consent of CRT.

  5. Assignment to CRT if protection withdrawn or abandoned: If the Host Institution decides to withdraw or abandon patent or similar protection in respect of Funded Intellectual Property, CRT shall be entitled to take an assignment of the property concerned and the Host Institution shall give CRT no less than sixty (60) days’ notice to allow it to do so effectively.

  6. No exploitation without prior consent: The Host Institution may not exploit, or grant any third parties the right to exploit, Funded Intellectual Property without the prior written consent of CRT. Where CRT consents to such exploitation, it may impose such conditions as it sees fit.

  7. Right to call for assignment to CRT: CRUK retains the right to call for an assignment to CRT of all Funded Intellectual Property. Such right is likely only to be exercised rarely. After such an assignment has been completed CRT and the Host Institution shall negotiate in good faith to agree the terms of a revenue share agreement in respect of net income received by CRT arising from the commercial exploitation of such Funded Intellectual Property.

  8. Commercial exploitation without consent: If, notwithstanding the prohibition in section 22, Funded Intellectual Property is exploited commercially without CRT’s prior written consent, the Host Institution shall:

    1. pay or transfer (as appropriate) to CRT sixty percent (60%) of all gross income and any other sums (whether in cash or otherwise) received by the Host Institution (or by any third party authorised by the Host Institution) from the exploitation of the Funded Intellectual Property, without any deduction of any costs, taxes or any other sums. However, if: (i) a third party contributes towards the directly incurred costs of the research which led to the creation of the Funded Intellectual Property; or (ii) CRUK provides additional funding (over and above the directly incurred costs), then the foregoing revenue share shall be adjusted as CRT deems appropriate;

    2. account to CRT for its revenue share on a quarterly basis, in pounds sterling;

    3. be solely responsible for rewarding the inventors of Funded Intellectual Property out of its share of gross income;

    4. provide CRT with a quarterly statement summarising all income received and costs incurred; and

    5. ensure that proper books and records are kept (recording all exploitation activities and all income received/costs incurred) and allow CRT access to such books and records as CRT may reasonably request from time to time.

  9. Transfer of samples: CRUK encourages the transfer of samples of Funded Materials to academic and other not-for-profit third parties solely for the purposes of non-commercial research, under the terms of a material transfer agreement. The Host Institution may not transfer Funded Materials to any commercial entity without CRT’s prior written consent.

  10. Retention of agreements: The Host Institution shall retain copies of all agreements (including collaboration agreements, material transfer agreements and confidential disclosure agreements) proposed and/or completed relating to Funded Intellectual Property. The Host Institution shall provide CRT with copies of such agreements as CRT may request from time to time.

  11. CRT contact: For further details contact: enquiries@cancertechnology.com.

 

Schedule B. Special conditions for policy and information targeted research projects

  1. Application: The Special Conditions in this Schedule B apply where a Grant is identified in the GAL as a ‘P&I targeted research project’. Unless otherwise specified, these Special Conditions apply in addition to the Grant Conditions.

  2. Intellectual property: For P&I targeted research projects, sections 11.2 and 11.3 and any TTA shall not apply to the Funded Intellectual Property. Section 11.1 shall apply and in addition the Host Institution hereby grants CRUK the perpetual and irrevocable right to use, and permit others to use, Funded Intellectual Property for:

    1. public policy and public information purposes on an exclusive basis, unless CRUK agrees otherwise; and

    2. academic research and teaching without restriction on a non-exclusive basis (with, for clarity, the Host Institution being able itself and in collaboration with third parties to undertake academic research and teaching).

Should the Host Institution receive monetary or non-monetary income directly or indirectly from the commercial exploitation of Funded Intellectual Property, then the Host Institution shall share such income, in a reasonable proportion, with CRUK.

  1. Project manager and key staff: The Host Institution will ensure that the Grant Activities are managed by a named project manager. The project manager and key staff members who will conduct the Grant Activities must be identified to CRUK before the Start Date, and may not be changed without consent from CRUK.

  2. Publications: In addition to the obligations set out in section 12 of the Grant Conditions, the Grantholder or Host Institution must send any publication of Results to CRUK for review at least four (4) weeks prior to submission for publication. They must also comply with any publications policy issued by CRUK.

  3. Payments and deliverables: Section 5.3 of the Grant Conditions applies in all respects save for frequency of payments. Instead, Grant payments will be made by CRUK in accordance with key deliverables and dates as set out in the GAL.