Clinical Data Management Course (CDM) is a procedure in clinical research that creates statistically sound data of top-quality and well-founded assuring and collecting at a precise rate and quality thereby managing conduct and analysis of trials across the process of clinical research. With the inflow of multinational players in Indian Clinical Research, India has become one of the dominant hubs of the profession leading the industry to grow exponentially and open up new vistas of employment for a large number of people.

What is Pharmacovigilance?

Pharmacovigilance is a branch of the pharmacy where vigilance is kept over the use of drugs. According to WHO guidelines, proper reporting of Adverse drug reactions, and Adverse events is necessary in order to completely justify the job of Pharmacovigilance. At present career in it is at boom and various institutes provide Pharmacovigilance courses.

Duties of Pharmacovigilance…

The Pharmacovigilance officers carry out a complete survey and report of ADR’S and AE’S regarding the drugs and their classifications during the whole course of the year and complete their job of reporting by filling up the forms online and submitting them to FDA and WHO.

RA is an industry that oversees how foods, drugs, and medical products are developed, tested, manufactured, marketed, and distributed to certify that they meet regulatory standards for human use. RA department of a pharmaceutical company is responsible for obtaining approval for new pharmaceutical products and ensuring that approval is maintained for as long as the company wants to keep the product on the market. RA professionals are responsible for ensuring manufacturers’ compliance with applicable global legislative and regulatory requirements at each stage of product development.