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.

Feasibility

Regulatory affairs

Startup

Safety reporting

Admin and logistics

Site space management

Project management

Quality management

Recruitment and retention

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50+ ERC and RA submissions

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100% success rate

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16 weeks average approval time

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Clinical Trial Guidelines