Assistance with R&D Approvals
During the lifetime of the clinical trial the R and D department may be involved in monitoring of the trial, audits of practice, aspects of pharmacovigilance, preparing an annual report/end of trial report and facilitating archiving of the trial. We collect, maintain and distribute essential documents as required by trial protocols.
Contract Negotiation
Researchers wishing to conduct research in the NHS must obtain local Research & Development (R&D) approval before your study can commence. If your study is a GP based study then local Primary Care Trust (PCT) approval is required. Here at The Ethics Company we can provide the necessary expertise to process the requirements of each individual R&D and PCT.
Services provided include:
- Information regarding costs relevant to each R&D/PCT( Overheads/Set up costs ect)
- Contract negotiation with each site
- Provision of all documentation required by the R&D /PCT departments.
- Confirmation of expected approval timelines.
