Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required)
Candidates Having The Central Drugs Standard Control Organization(CDSCO) experience and similar with these organizations can apply .
Informing strategic regulatory controls and providing the worldwide regulatory policy for product development, manufacturing, and registration: It aids the applicant in advancing a universally accepted product.
Development of proper leaflets like a summary of product characteristics, patient information, etc.
To complete record data of the company’s products and maintain the records of therapeutic products in agreement with current regulations and guidelines.
To prepare data about a new product for doctors and other healthcare professionals for harmless and effective practice of medicine and maintain records, and reports of post-marketing surveillance of the new product. It also helps to prepare the leaflets and advertising material for existing as well as new drugs.
IMMEDIATE JOINERS CAN APPLY.