The Regulatory affairs team in Synmedic Laboratories has a high level of proficiency, and, it has played a key role in earning registrations of products across the globe. This sound technical backup gives further impetus to the business development activities.

The company has in-house capability to prepare Dossiers of the products as per CTD format, and various other requirements of different countries. Most of our formulations undergo clinical trials for Bio-Availability and Bio-Equivalence studies at reputed Clinical Research Organizations. Data from these studies is utilized to enhance the effectiveness of these formulations, which are part of our Dossiers.

The regulatory team at Synmedic has obtained more than a hundred registrations across the globe based on their proficient capabilities.