Jatinder Singh Mahant
General Manager | Regulatory Affairs
M. Pharm
"Understanding of the current regulatory requirements of different Regulatory authorities worldwide to explore the new regulatory challenges and pathways; helps to manage life cycle management of the Pharmaceutical products with the Regulatory agencies worldwide."
Years at VMRC
The pharmaceutical research and development process of bringing a new drug technology to the market takes many years; it is, therefore, essential that the process is managed effectively from beginning to end in order to meet the current worldwide regulatory requirements. Regulatory affairs act as the key interface between the company and the regulators. Regulatory affairs involve extensive evaluation of a particular drug product by promotion, registration, marketing and post-marketing activities of the drug product. One of the vital activity of the regulatory specialist is to ensure that; all the information pertaining to the medicines have been correctly established.
Our focus is to be a global reference and driving force in the evolution of healthcare sector, offering the best environment for the individual and collective growth of our team and clients and to provide solutions for regulatory challenges which allow both flexibilities for the client and compliance with the relevant legislation without becoming over complicated.
- Department of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala, India, Bachelor of Pharmacy – 2003
- Vinayaka Mission Research Foundation, Vinayaka Mission University Salem, TN, India Masters of Pharmacy – 2005.
