This is a pharmaceutical manufacturing company, owned by an international American firm McGaw. It’s mainly concerned in manufacturing parenteral dosage forms. It has a number of sterile manufacturing units, whereby full GMP rules are implemented.
Responsibilities:
- Documentation of the product’s pharmacological, toxicological and clinical studies.
- Acted as an expert in assessing the product’s development as well as the pharmacological and toxicological part of the dossier.
- Tabulating the study report in the required manner.