Indian Biological-science and Research Institute

Comprehensive Program in Regulatory Affairs for Pharmaceutics [12 Months]

Indian Biological-science and Research Institute
  • Indian Biological-science and Research Institute

Originalpreis in INR:
₹ 14.500

Wichtige informationen

Tipologie Kurs
Methodologie Fernunterricht
Dauer 12 Months
Beginn nach Wahl
Versendung von Lernmaterial Ja
Beratungsservice Ja
Präsenzprüfung Ja
  • Kurs
  • Fernunterricht
  • Dauer:
    12 Months
  • Beginn:
    nach Wahl
  • Versendung von Lernmaterial
  • Beratungsservice
  • Präsenzprüfung

Emagister added to its educational catalogue the Comprehensive Program in Regulatory Affairs for Pharmaceutics [12 Months] course endorsed by Indian Biological-science and Research Institute.

With this programme, you will understand the fundamentals and concepts of regulation prevailing in various countries and you will enhance your knowledge and skills in the field of Regulatory affairs.

The objectives of this course are to create experts in the field of RA documentation and research, to encourage continuous learning and development in RA field and to update knowledge of existing RA professionals.

This course is suitable for: B Pharmacy/ M Pharmacy/ Science Graduate with working experience.

Join this course now! if you want to learn more information about it, do not hesitate to contact Indian Biological-science and Research Institute through

Wichtige informationen
Welche Ziele verfolgt der Kurs?

The courses will provide integrated knowledge and broad perspectives you need to effectively manage the regulatory process from Innovation →Discovery → Approval→ Commercialization which implies regulatory affairs are essential to bring the product to the market globally.

To gain the essential knowledge and skills required to help companies to work in regulatory environment.
To acquire the foundation to work within or in variety of areas including medical products development, pharmaceutical formulations, sales, strategic marketing and clinical investigations.
To know about regulatory process in drug development, formulations, API.
To sharpen the understanding of the laws that governs the development, manufacturing and commercialization along with the distribution of drugs, biologics and medical devices.

Ist dieser Kurs für mich?

This course is aimed at participants who want to join Regulatory Affairs as career.

Wie geht es nach der Info-Anfrage weiter?

After receiving your request our team member will contact you and mail you all related information.

Voraussetzungen: Post Graduate in Life-science or Pharma OR Graduate in Life-science with work experience in similar domain.



Distance Learning


nach Wahl Anmeldung möglich

Was lernen Sie in diesem Kurs?

Pharmacy Technician
Pharmacy Assistant
Pharmaceutical Marketing
Regulatory Compliance
Pharmaceutical manufacturing
Regulatory Affairs


Here is the course papers
Introduction to Regulatory Affairs and Profession
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