Regulatory Affairs
A key factor in conducting clinical trials is timely submissions to the Regulatory Authority. In addition, choosing the right ERC for faster approval and timely submission is essential for on-time recruitment. RemediumOne has its own in-house Regulatory Affairs department, with a good track record of ensuring timely and accurate submissions to all ethics review committees and the Regulatory Authority in Sri Lanka.

50+ ERC and RA submissions

100% success rate

16 weeks average approval time
