Over the years Evolet has a team of highly committed and experienced Regulatory affairs professionals. It reviews in house documentations and updating other departments. It is the interface between the company and the regulatory authorities.
It assures the efficacy, safety, and quality of the product. Regulatory Affairs is involved in the development of new medicinal products, by applying regulatory principles and by preparing and submitting the relevant regulatory dossiers to health authorities within the specified time period.
Our Regulatory Team has an invaluable experience in the market for the manufacture of high quality products.
Our regulatory team keeps track of and updates the company with the always changing regulatory guidelines / requirements of the region.
Evolet have Common Technical Document (CTD) dossiers, enabling compliance with various health authorities.