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Comprehensive Program in Regulatory Affairs for Pharmaceutics [12 Months]

4.3
3 Meinungen
  • Excellent place to be.
    |
  • I figured faculty is amazing, IBRI is one of the best institute of biological science and information.
    |
  • The main point why I've choosen this place is because of its nurturing environment. Ajay Sir helped a lot in the project in my first research project. I had a good experience and its a good training institute would recommend the same to all.
    |

Kurs

Online

659 €

*Richtpreis

Originalbetrag in USD:

$ 800

Beschreibung

  • Kursart

    Kurs

  • Methodik

    Online

  • Dauer

    12 Months

  • Beginn

    nach Wahl

  • Versendung von Lernmaterial

    Ja

  • Beratungsservice

    Ja

  • Präsenzprüfung

    Ja

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 Emagister.co.uk

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 Informationsanfrage 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.

Standorte und Zeitplan

Lage

Beginn

Online

Beginn

nach Wahl Anmeldung möglich

Meinungen

4.3
fantastisch
100%
4.6
ausgezeichnet

Kursbewertung

Empfehlung der User

Anbieterbewertung

User

09.07.2020
Über den Kurs: Excellent place to be.
Kurs abgeschlossen: Juli 2020
Würden Sie diesen Bildungsanbieter weiterempfehlen?: Ja

YOGEN PARMAR

10.07.2020
Über den Kurs: I figured faculty is amazing, IBRI is one of the best institute of biological science and information.
Kurs abgeschlossen: Juli 2020
Würden Sie diesen Bildungsanbieter weiterempfehlen?: Ja

RAGHU

11.07.2020
Über den Kurs: The main point why I've choosen this place is because of its nurturing environment. Ajay Sir helped a lot in the project in my first research project. I had a good experience and its a good training institute would recommend the same to all.
Kurs abgeschlossen: Juli 2020
Würden Sie diesen Bildungsanbieter weiterempfehlen?: Ja
*Erhaltene Meinungen durch Emagister & iAgora

Themen

  • Pharmacy Technician
  • Pharmacy Assistant
  • Pharmacology
  • Pharma
  • Pharmaceutical Marketing
  • Pharmacist
  • Regulatory Compliance
  • Pharmaceutical manufacturing
  • Regulatory Affairs
  • DRA

Inhalte

Here is the course papers
Paper-I:
Introduction to Regulatory Affairs and Profession
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

Comprehensive Program in Regulatory Affairs for Pharmaceutics [12 Months]

659 €

*Richtpreis

Originalbetrag in USD:

$ 800