Regulatory Affairs department is an important part of the organizational structure of our company. Regulatory Affairs professionals play an essential role in ensuring all our products comply with complex regulations governing the industry, which continuously undergo amendments and supplementation. They are not only involved in the initial application phase for a drug, but also in the licensing and later stages, making sure all operations and products meet required safety and efficacy standards.
Patient protection is of great importance.
Handling a number of different tasks, both online and off, from keeping informed of the developments within the industry to writing product labels and patient leaflets, they collect and collate large amounts of information and prepare licensing submissions in tight deadlines.
Our Regulatory Affair professionals are committed to quality and continual improvement being the key interface between the company, our products and regulatory authorities.