We have been asked to explore and share the site set up practice, challenges, and improvement suggestions of NHS R&D departments when setting up commercially driven studies as sites. Our findings will be shared with industry colleagues, NIHR CRNCC, HRA and the devolved administrations. We will not share any identifying information. 

Please share your views and a wish list of what you would like to see to improve the set up of commercial studies in the UK. This might include your experience of starting up new industry studies including for example: industry & CRO processes, Capacity and Capability, mCTA sign-off, implementation of protocol amendments etc.

The survey will be open until the 14th December. 

Thank you
 
Tracy Assari, Kate Greenwood

 

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* 1. Your name (optional)

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* 2. Your role

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* 3. Your contact email (optional)

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* 4. Your organisation name (optional)

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* 7. How would you describe the study set up process for commercial studies when it works well?

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* 8. What are the main issues you find when setting up commercial studies?

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* 10. If you don’t always get a Local Information Pack what documents are frequently missing?

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* 11. How do find the electronic version of the costing template works/integrates with your study set up processes? Please give details

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* 13. If yes, you do execute and exchange the contract prior to issuing C&C, is this due to:

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* 14. What would be on your wish list for a more streamlined set up?

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* 15. Without naming the company please can you provide live examples of particular issues you have encountered regarding the set up of commercial studies in relation to themes such as contracting, budget costing, amendments, communications and timelines.

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* 16. What additional support would you like in this area?

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