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Certificate Course in Regulatory Affair

Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in regulatory affairs is required.

PRLog - Jun. 13, 2014 - NOIDA, India -- Special Features of this Program: - It includes the maximum syllabus of RAC Certification for Regulatory Affairs Professionals.

Course Highlights:-
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 ofDMF, Dossiers etc.)
Paper IV: Global Regulatory Compliance Systems

Eligibility: - Any Science graduate / Pharmacy graduate / Medical graduate / Life-science graduate OR working professionals in same field.

Duration of Course: - 6 Months
Mode of Course: - Distance Mode Education

Special Features of this Program: - It includes the maximum syllabus of RAPS certification for Regulatory Affairs Professionals.

Course Fees: - Rs 7000/-(Indian Student)

Study Material for the course: - Complete study material will be provided by the institute in printed book form.

How to pay the course fees: - Course fees can be paid
·By Demand Draft in favour of "IBRI- Unit of Exordior Technical Services Pvt Ltd" and payable at "NOIDA".
·By cheque in favour of "IBRI- Unit of Exordior Technical Services Pvt Ltd".
·By NEFT to institute account.
·By cash at IBRI NOIDA.

Examination and Evaluation Process: - One time examination and mode of examination are

·Assignment Based Examination

·Examination Center based Examination

·Evaluation by experts from industry and academic team of institute.

How to join this course?

·Download Registration Form from website

·Fill it completely and attach 10th, graduation and one photograph for ID card.

·Send it by Registered Post or Courier only.


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Contact Email:
***@ibri.org.in Email Verified
Location:Noida - Uttar Pradesh - India
Tags:Drug Regulatory Affair, Pharma Regulatory Affair, ich gcp
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