To know more about regulatory submission procedures, IPM is the best learning platform for the last 13 years.
Pharmaceutical and clinical industry is the most regulated among all the industries. Every drug before getting market approval must undergo rigorous scrutiny and clinical trials to ensure its safety, efficacy and quality. These standards (regulations) are set by regulatory authorities of respective countries.
Regulatory affairs [RA] is a department in the pharma industry.
Importance of regulatory affairs:
Qualities of a good RA professional
How to keep up with the constantly changing regulatory landscape?
Certificate courses in Regulatory Affairs at IPM
Institute of Pharmaceutical Management (IPM) in Mumbai endows progressive post-graduate diploma in the realm of regulatory affairs to discover positions such as Regulatory affairs associate, Regulatory affairs officer, Regulatory affairs executive, Regulatory affairs manager, to name a few. Its courses are self-paced and been intended by the industry specialists to fulfill the end-to-end requirements of tirelessly developing pharmaceutical companies and various other federal agencies.
IPM offers personalized classroom activities by way of a Tutoring Centre, Excellent Tutoring and other opportunities.
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