A proven pathway to ethics approval and trial success
Accelagen’s extensive, in-house regulatory and clinical knowledge sets our partners up for approval success.
We critically assess relevant scientific data and develop tailored solutions. This mitigates risk during Ethics reviews and gives you the best chance of timely approval. With hundreds of approvals to date, Accelagen gets studies starting off on the right track, minimising delays, and allowing patients treatment to commence sooner.
- Regulatory and Ethics submission preparation and management
- Strategic gap analysis and solution development
- Drafting and Quality Oversight of Core Regulatory documentation
- Regulatory and Ethics submission lifecycle management
- Liasion between Sponsor and Ethics Committee/Regulatory Agency
How we work
Proven expertise in ethics approvals
Our decades of experience takes the guess work out of the submission process, setting you up for approval success.
Clear and consistent communication
Your dedicated Project Manager keeps you informed every step of the way.
Solving risks – before they happen
We identify and mitigate challenges before they occur, saving you the time and cost of a lengthy ethics approval.
Human research ethics committee submissions
case studies
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