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Global HR Head Wockhardt during Diploma Award Ceremony at Aurangabad
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What’s Student Say?
Hi, Dr. Burande, I am excited and pleased to let you know that I took I.P.E.R.'s Diploma in Drug Regulatory Affairs - D.D.R.A course when I was pursuing my M.Pharm. in 2009. With this course, I was able to join Alembic Pharma Regulatory Dept. and now after 7 years of working experience, I am Team Lead – Regulatory Affairs for US and EU market in MNC Colgate – Palmolive based at Mumbai. I started my career at 2.00 Lakh per annum from Alembic and currently reached to 13.00 lakh per annum at Colgate – Palmolive. I am very much thankful for setting up such a nice platform for me on which I can stand still today.
Ruchir ShahTeam Lead – Regulatory Affairs for US and EU market in MNC Colgate – Palmolive based at Mumbai
I successfully completed MPDM (Diploma in Project Management, Diploma in Drug laws, Diploma in Drug Regulatory Affairs ) in 2008. Project management diploma was useful to understand Project requirements of Pharma Plant operational. Drug laws diploma was useful to understand various drug schedules, drug laws and their importance for industry. Drug regulatory affairs course was useful to understand Drug master file requirements and involvement of cross functional teams of R&D, ADL, QA, QC, Project and Regularity teams.
Dr. Swarup Prabhune,
Group Leader (API-ADL), Cipla Ltd.
I am B.Sc. and completed DPQCQAM Course in 1992. During that time I was in a small company and my salary was 2000 Rs. After doing this programme because of knowledge and skill company given me 2000 Rs. of course fee and 1000 Rs. increment. My Career started. Now I am with Alkem GM Quality Control USFDA Approved plant and 600 people working under me with extra ordinary package. Thanks to IPER for marking my successful career.
Aajay Kumar Singh,
General Manager Q.C. Alkem Laboratories, Baddi
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