Regulatory Services

Aura research Services has expertise and experience to provide a full range of Pharmaceutical regulatory affair solutions and is dedicated to delivering the highest quality support, helping your company to gain speedy approvals for your medicine pipeline in a timely and cost-effective manner.

Our Subject matter experts with extensive experience can provides you with services for Clinical Trial Approvals, Managing safety reporting during all aspects of clinical trials, post-marketing surveillance and consulting for Market Authorizations (MA), Product and Site Registrations in Health care domain.