TopPharm Consulting:

Regulatory affairs for medicinal products or medical devices is a complex process. Each country in Europe has its own specific requirements related to medicinal products, medical devices or food supplements. Knowledge of such county-specific regulations is crucial to get marketing authorization or to solve other regulatory problems smoothly and quickly. It helps also to foresee and prevent from potential problems by choosing the right solutions in advance not during the authorization process when all problems and clarifications result in huge delays. Our services help to avoid such dead ends which is of great importance to company marketing plans.


Medical device, Regulatory Affairs






© 2015 The World of CROs. All rights reserved.