Comprehensive Program in Regulatory Affairs for Pharmaceutics [12 Months]
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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.
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I figured faculty is amazing, IBRI is one of the best institute of biological science and information.
← | →
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Excellent place to be.
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Training
Online
*Indicative price
Original amount in USD:
$ 800
Boost your career with this course!
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Type
Training
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Methodology
Online
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Duration
12 Months
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Start date
Different dates available
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Delivery of study materials
Yes
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Support service
Yes
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Examinations- physical attendance required
Yes
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
Facilities
Location
Start date
Start date
About this course
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.
This course is aimed at participants who want to join Regulatory Affairs as career.
Post Graduate in Life-science or Pharma OR Graduate in Life-science with work experience in similar domain.
Post Graduate in Life-science or Pharma OR Graduate in Life-science with work experience in similar domain.
This program will upgrade you to enter or promote in Regulatory Affairs domain.
After receiving your request our team member will contact you and mail you all related information.
Reviews
-
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.
← | →
-
I figured faculty is amazing, IBRI is one of the best institute of biological science and information.
← | →
-
Excellent place to be.
← | →
Course rating
Recommended
Centre rating
RAGHU
YOGEN PARMAR
User
Subjects
- Regulatory Compliance
- Regulatory Affairs
- DRA
- Pharma
- Pharmacist
- Pharmacology
- Pharmacy Technician
- Pharmaceutical Marketing
- Pharmaceutical manufacturing
- Pharmacy Assistant
Teachers and trainers (1)
Dr.Shikha Mishra
Manager -DRA
Course programme
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]
*Indicative price
Original amount in USD:
$ 800