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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

Clinical Trial Guidelines

RemediumOne (Pvt) Ltd.

No 41/10, Guildford Crescent,
Colombo 07, Sri Lanka

+94112665266

+94112665300

inquiries@remediumone.com

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