Please provide me syllabus of Diploma in Regulatory Affairs.

[vikash]

Here I am providing you information about post graduate Diploma in Regulatory Affairs.

Duration

Diploma in Regulatory Affairs diploma duration is 6 month

Requirements
Here I am providing you eligiblity for this diploma. For joining this diploma you must have graduate and postgraduate degrees like these MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B.Pharma.

Syllabus

This diploma is specially designed for the students would like to develop their
career in the field of regulatory.

Program would include

Introduction to Regulatory Affairs
Pharma Regulations Practices & Procedures
Import and Export of Drugs in India
Good Manufacturing Practice
Quality Assurance and Regulation
Introduction to Clinical Research
Principles of Good Clinical Practices
Ethical Considerations in Clinical Research
Indian Regulatory Environment
Future of Regulatory Compliance
Orphan Drugs
Regulation In Pharmaceutical Devices
Trips and Pharma Industry
Biomedical Intellectual Property Management
Patent Application Processing Flowchart

i would like to study

hi i like to study address? my email sharathnandha91@gmail.com

Sir Please send me any link or broucher of this drug regulatory affairs course so i can check its fees and how to take admission.

Originally Posted by vikash

Here I am providing you information about post graduate Diploma in Regulatory Affairs.

Duration

Diploma in Regulatory Affairs diploma duration is 6 month

Requirements
Here I am providing you eligiblity for this diploma. For joining this diploma you must have graduate and postgraduate degrees like these MD, MS, MBBS, BDS, BHMS, BAMS, BUMS, BPT, B.Pharma.

Syllabus

This diploma is specially designed for the students would like to develop their
career in the field of regulatory.

Program would include

Introduction to Regulatory Affairs
Pharma Regulations Practices & Procedures
Import and Export of Drugs in India
Good Manufacturing Practice
Quality Assurance and Regulation
Introduction to Clinical Research
Principles of Good Clinical Practices
Ethical Considerations in Clinical Research
Indian Regulatory Environment
Future of Regulatory Compliance
Orphan Drugs
Regulation In Pharmaceutical Devices
Trips and Pharma Industry
Biomedical Intellectual Property Management
Patent Application Processing Flowchart

Sir, please send me fees and how to take admission for this course along with official website.