UNILINK is well aware that all the government drug regulatory agencies across the globe wants to ensure that all products made available to its people conform to acceptable standards of quality, safety, and efficacy.
Have registered several our pharmaceuticals in the markets we are present. Our highly experienced registration department deals with all matters relating to the registration of our products. Our customers rely on our experience and competent staff to complete product registration effectively and efficiently.
We have a large team of Pharmacists, Science graduates and microbiologists working in our regulatory department and are abreast with the specification of each country and also to compile CTD dossiers.
Inspection of manufacturing facilities on the basis of compliance with GMP is a vital element of drug control.
UNILINK supports WHO initiatives aimed at improving inspection and will always try to increase the frequency and number of inspections by the inspectors from Ministry of Health and Pharmacy Board of various countries.
Proper documentation is essential in almost every aspect of the pharmaceutical industry. Whether for product registration, factory inspection, or internal quality control, UNILINK employs the latest technologies to streamline and process information.
UNILINK has WHO-(GMP). Essential product registration documents, such as the Certificate of Pharmaceutical Product (COPP), Free Sales Certificate (FSC), Certificate of Origin (COO), and Marketing Authorizations, CTD Dossiers are among the many documents our registration department frequently submits for registration purposes.