We follows GMP, GLP recommendations and fulfills the standards of the Regulatory authorities. The applications of the IH standards, as well as the issuing and updating of all the technical documentation are coordinated by QA, QC & RA coupled with the internal & external audits and work hand-in-hand to accomplish best standards.
Product development activities are headed by well experienced professionals having extensive knowledge on different polymers behavior and their usage in the Drug delivery systems. Scoat Pharma has dedicated areas for product development and scale up studies before commercialization. At Scoat Pharma, Product development activity is an on-going process and statistically compare the in-vitro drug release profiles against the originator products or as per market samples, where required we develop the products as per customer needs or in-house specifications based on literature.