Diploma in Drug Regulatory Affairs

Certificate

Distance

₹ 14,500 + VAT

Description

  • Type

    Certificate

  • Methodology

    Distance learning

  • Duration

    12 Months

  • Internship

    Yes

  • Online campus

    Yes

  • Delivery of study materials

    Yes

  • Support service

    Yes

  • 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

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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

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

₹ 14,500 + VAT