At IPM, we offer PG Diploma in Regulatory Affairs for Drugs (API & Formulation) which help to prepare students in the field of global regulatory submissions. We have strong presence in Mumbai- Borivali, Vashi and Dombivli. Existing pharma professionals can refine and boost their knowledge of global regulatory affairs by joining our courses. Our Post Graduate Diploma in Regulatory Affairs is designed as per current regulatory requirements (FDA, EMA, PMDA, India, Health Canada, WHO, ASEAN) to gain expertise in the field of pharmaceutical regulatory affairs.
3. Anagha Maharao
Managing Director
30 years of pharma
experience
Principal trainer for
RA & QA topics
GMP & RA consultant with
renowned pharmaceutical
organizations
Audits & compliance expert
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4. Courses available
Regulatory affairs
Regulatory aspects of
International Business
DMF & Dossier review
Anagha Maharao with team of experienced faculties
from industries conduct these training programmes
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5. Types of training
Classroom sessions at
Dombivli, Borivali & Vashi
Distance learning courses
On site training [at company premises &
colleges]
Seminars/workshops
at various locations
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6. Achievements
13th year of ‘Excellence in training’
Over 5000 enrolments
Students placed in renowned companies
Enrolments from Japan, Spain, New York, Australia
Vietnam, South Africa, UK ,Oman, Dubai ,
Johannesburg, Bangladesh,
Abu Dhabi, Armenia
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7. Achievements (contd..)
Trained 75 participants of AstraZeneca , Bangalore
on RA
Trained Novartis warehouse team on GDP
Conducted training programmes at FDC,
Polypeptides, IDA Foundation, Bharat Parenterals,
IDMA-Vadodara , Sipra Labs & more
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