Diploma in Drug Regulatory Affairs
Certificate
Distance
Description
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Type
Certificate
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Methodology
Distance learning
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Duration
12 Months
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Internship
Yes
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Online campus
Yes
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Delivery of study materials
Yes
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Support service
Yes
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Virtual classes
Yes
Comprehensive Program in Regulatory Affairs for Pharmaceutics [12 Months]
Paper-I: Introduction to Regulatory Affairs
Paper-II: International Licensing and Drug Regulatory Affairs
Paper-III: Regulatory Documentation for Biologics/Medical Diagnostics and Pharmaceutics (Submission of DMF, Dossiers etc)
Paper-IV: Global Regulatory Compliance Systems
Paper-V: Regulations for Clinical Trials, GMP, GLP and ICH Guidelines
Paper-VI: Regulatory Strategy and Quality Assurance Systems
Paper-VII: Future of Biopharmaceuticals
Paper-VIII: Research Study
About this course
Helpful for jobs,enhancement of profile quality,Getting more and accurate interview calls for pharmaceutical regulatory professionals.
Any Graduate or Undergraduate can join this course.MBBS,BDS,B.Pharmacy,M.Pharmacy,B.Sc,M.Sc,B.Tech,M.Tech,etc
Any Graduate or Undergraduate can join this course.MBBS,BDS,B.Pharmacy,M.Pharmacy,B.Sc,M.Sc,B.Tech,M.Tech,etc
Reviews
Subjects
- Regulatory Compliance
- Compliance
- Research
- World Affairs
- Quality Assurance
- International
- DMF
- Dossier
- DRA
- RA
- Diploma in Regulatory Affairs
- International regulatory affairs
Teachers and trainers (1)
Dr.Kumud Sarin Sarin
Director
Having degree like Ph.D,PDF with 20+ tears of experience. Already running number of books for Following Course.. Drug Regulatory Affairs Pharmacovigilance Clinical Research Bbiostatistics,Epidemiology and Research Methodology ...etc
Course programme
Comprehensive Program in Regulatory Affairs for Pharmaceutics [12 Months]
Paper-I: Introduction to Regulatory Affairs
Paper-II: International Licensing and Drug Regulatory Affairs
Paper-III: Regulatory Documentation for Biologics/Medical Diagnostics and Pharmaceutics (Submission of DMF, Dossiers etc)
Paper-IV: Global Regulatory Compliance Systems
Paper-V: Regulations for Clinical Trials, GMP, GLP and ICH Guidelines
Paper-VI: Regulatory Strategy and Quality Assurance Systems
Paper-VII: Future of Biopharmaceuticals
Paper-VIII: Research Study
Diploma in Drug Regulatory Affairs