The requirements of pharmaceutical companies and international regulations have increased in the area of Regulatory Affairs, Pharmacovigilance and Compliance.
TRIDEM Pharma has developed high added value expertise for such activities.
A head-office and local team to help you register your products…
TRIDEM Pharma’s Regulatory Affairs department will prepare a dossier that meets the requirements of each country, based on a standard dossier supplied by the laboratory. It monitors file submissions with Pharmaceutical and Drug Authorities working with its dedicated team in the field.
The TRIDEM Pharma dedicated team has developed expertise in pharmacovigilance. It provides a service to our partner laboratories for monitoring their products sold in assigned areas, in compliance with local regulations.
…Quality and Compliance
The level of quality and compliance of TRIDEM Pharma is recognised by our international partner laboratories and regularly audited.