Yes you will get complete solution for your product from initiation to development and growth to maturity. We are expertise in giving you back quality clinical data and then we can compile and file e-CTD dossiers anywhere in the world.

We will guide you to design prelaunch and post launch plan after getting new drug approval along with promotion inputs like product monograph, brochure, visual aid, newsletter and product training.

We can assist you in designing artwork, patient leaflets, summary of product characteristics and product manual

Pharmacovigilance is now utmost important in almost all countries of the world to take care patient first and then product life cycle. We can support in compiling Independent Case Study Report, Periodic Safety Update Report, Risk Management Planning, Periodic Benefit Risk Evaluation Report, Periodic Adverse Drug Experience Report, Pharmacovigilance System Master File, System Set up and implementation along with audit and training.