Certificate in Drug Regulatory Affairs Study
Certificate
Online
Description
-
Type
Certificate
-
Methodology
Online
-
Duration
1 Year
-
Start date
Different dates available
-
Online campus
Yes
The purpose of this programme is to provide graduate/post graduate level education in the important aspects of legal and regulatory issues that are critical to the pharmaceutical industry. The course focuses on key legal concepts such as intellectual property and the range of regulatory affairs with which the pharmaceutical industry must comply and strategies for attaining so.
Facilities
Location
Start date
Start date
About this course
• To develop understanding of legal and regulatory issues of pharmaceutical industry. • To enhance regulatory knowledge and sharpen regulatory skills. • To provide students with the national and international drug regulations.
B. Pharm, M. Pharm, B.Sc, M.Sc and Researchers
• 2 Passport Size Photos • Photo ID Proof • Address Proof • All Experience Certificates • All Education Mark sheet and Certificates • Resume
B. Pharm, M. Pharm, B.Sc, M.Sc and Researchers
ONLINE STUDY SELF LEARNING PROGRAM
ONLINE APPLICATION REGISTRATION DETAILS
Reviews
This centre's achievements
Subjects
- Patent Law
- Practice and Procedure
- Industrial IPR Design &Trademark
- International
- IT Industry
- Legal
- Intellectual Property
- World Affairs
- Pharmaceutical
- Drug Interaction
Teachers and trainers (1)
SNEHA SHARMA
ENGINEERING JOBS
Course programme
Module I : Introduction to Intellectual Property Rights
Module II : Patent Law, Practice and Procedure
Module III : Industrial IPR Design &Trademark
Module IV : Indian Drug Regulations
Module V
:
International Drug Regulations
ModuleVI
:
WTO, GATT, IPR, TRIPS, Orange book guidelines, EMR, GMP, GLP, US-FDA & ICH Guidelines.
• Comparison of Indian Regulatory requirements with Global standards.
Certificate in Drug Regulatory Affairs Study