Description
Techno Bridge offers Expert Designed Practical Regulatory Affairs Courses for Professionals & Job Seekers. All our candidates pursue regulatory affairs training programs for different reasons. For professionals, it is an add-on to their existing skillset. CRO owners can use these skills to enhance their business. Whereas these skills help job seekers get a job. Therefore, our courses are structured to meet the needs of different students.
Details
- Listing categories Medicine / Pharmacy
- Location / Region India (IN)/ Pune
- Course Location: Online
Courses & Fees
Course Fee
$220
Other Courses
TechnoBridge is the best training institute for Pharmacovigilance courses with 100% Placement in Pune. Pharmacovigilance is a branch of clinical research that has promising career opportunities in the future. The course curriculum of the Pharmacovigilance courses at TechnoBridge is designed by experienced professionals in the field. The course content is developed as per the industry standards and regulations of clinical research. the course is the perfect suit for students who are willing to pursue a career in the healthcare research industry.
Course Name
Regulatory Affairs Courses
Course Description
TechnoBridge is the best training institute for Regulatory Affairs Courses with 100% placement assistance in Pune. The course curriculum of the Regulatory Affairs Courses in India is developed by experienced corporate experts. The course content is designed as per the ongoing needs and regulations of clinical research. TechnoBridge gives 100 % job assistance to the candidates. Students get many opportunities for jobs as well as a business once they complete their Regulatory Affairs Courses in Pune Successfully.
Features
List Hiring Companies
Drug Regulatory Affairs are a specialized type of regulatory affairs that are concerned with the promotion and marketing of pharmaceuticals. The scope of Drug Regulatory Affairs is to ensure that drugs are safe and effective, and that they have been manufactured according to the current Good Manufacturing Practices (GMP). Drug regulatory affairs are one of the most important departments in a pharmaceutical company. They have to ensure that the drugs they manufacture are safe for consumption, as well as ensuring that they meet all quality standards.
Education Type
Education level
Education Subject
Health and Safety, Health and Medicine, Biology, Chemistry and Physics
Duration
3 Months
Eligibility
Bachelor of Life Sciences
Accredited by
TechnoBridge Systems Pvt Ltd
Payment Option
Cash, Installment, Online Payment
Study Material
Yes - Provided by Institute
Placement
List Hiring Companies
Drug Regulatory Affairs are a specialized type of regulatory affairs that are concerned with the promotion and marketing of pharmaceuticals. The scope of Drug Regulatory Affairs is to ensure that drugs are safe and effective, and that they have been manufactured according to the current Good Manufacturing Practices (GMP). Drug regulatory affairs are one of the most important departments in a pharmaceutical company. They have to ensure that the drugs they manufacture are safe for consumption, as well as ensuring that they meet all quality standards.
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