This document provides information about the Institute of Regulatory Affairs and Quality Assurance (IRAQA), a joint venture between Sitabai Thite College of Pharmacy and Pharma QA. IRAQA offers classroom and distance learning courses in pharmaceutical regulatory affairs and quality assurance. The courses are designed by industry experts to provide practical knowledge and bridge the gap between academia and industry. IRAQA works with several leading Indian and international pharmaceutical companies to provide students with placement assistance upon completion of the programs.
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Regulatory and Quality Courses
1. Institute of Regulatory Affairs and Quality Assurance A joint venture of SITABAI THITE COLLEGE OF PHARMACY and PHARMA QA (Group managed by Cyclone Pharmaceuticals, Pune)
2. INTRODUCTION IRAQA established with a Industrial and Practical Approach of Pharmaceuticals Education. Classroom and Distance learning course in Pharmaceutical Regulatory Affairs & Quality Assurance.
8. Managed & run by the ShriChhatrapatiSambhajiShikshanSanstha, Shirur.
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10. Admission Procedure Form obtain from SitabaiThite College of Pharmacy, Shirur or Fill up online. Form Fee : Rs. 250/- DD/ Cheque in favor of “PHARMA QA” payable at Shirur. Study material will be delivered within 21 days from receipt of Admission fee. Course schedule and dates of lectures declared on institute website. www.iraqa.in email: info@iraqa.in
11. Course Directors Mr. SachinBhalekar B. Pharm MBA Worked with Dr. Reddys Lab, Cipla, Mission Vivacare Ltd. Pharma Consultant with Cyclone Pharma Pvt. Ltd. Promotor of Pharma QA group Prof. D. G. Baheti. M Pharm (Ph.D) Principal, SitabaiThite College of Pharmacy, Shirur Having experience more than 19 years .
12. Need of Courses of RA & QA India may lead world Pharmaceuticals around 2020. Today’s changing scenario in GMP & Registration guidelines. Need to bridge between Industry and academic sector. Need of updating knowledge of students as concern with industrial approach.
13. Why IRAQA Diploma Courses are designed to deepen your understanding of current regulations and their practical application in the development and commercialization of drugs, biologics, and medical device products. Provides the integrated knowledge and broad perspectives you need to effectively manage the regulatory process.
22. Faculty Technocrats from Industries. R & D Scientists. Directors of Leading Pharma Companies. Doctors and Physicians and some clinical experts. Academic experts.