Company brochure

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IPM is a pioneering training institute established in 2007. It offers services in:

Training
GMP consultancy
Regulatory Submissions

Mrs. Anagha Maharao – Managing Director & founder

  • Principal trainer, GMP & RA Consultant, Audit expert
  • 26 years of industry experience
  • Trained pharma professionals from fresh graduates to senior management on regulatory and GMP aspects

Achievements

  • Received over 3000 enrollments for classroom programmes
  • Conducted on site training at Astrazeneca, FDC, Polypeptides etc
  • Several International enrollments from Spain, New York, UK, South Africa, Vietnam, Oman, Dubai & Johannesburg
  • Audited US organization to evaluate Quality System
  • Successfully restored CEP of Indian company in March 2013
  • Filed DMFs and Dossiers with various regulatory agencies

Professional experience

  • 30 years in QC, QA and RA of API and formulation companies

Present Profile

  • Managing Director & Principal trainer at Institute of Pharmaceutical Management for QC, QA and RA courses since 2007
  • GMP and RA Consultant to renowned pharmaceutical organizations for 10 years.

8 years of excellence in Training & Consultancy!!!

Types of training
  • Classroom at IPM locations
  • Distance participation
  • In-house training for company employees
Courses offered
  • Drug Regulatory Affairs
  • International Business Development
  • Analytical Data Review
  • Quality Assurance
  • Quality Control
  • Patent Laws
GMP compliance
  • Review of analytical incidence, OOS, OOT.
  • Set up of new QC laboratory
  • Upgradation of existing QC
  • GMP compliance for API & Formulation – a complete project
  • Audits
  • Validation
  • Data integrity management
  • Software validation approach
Reg submissions
API
  • Preparation and submission of DMF to regulatory agencies
  • Gap analysis of ready DMF
Formulation
  • Dossier writing for emerging markets [Asia, Africa, Latin America, Central America & CIS countries]
  • ICH CTD, ASEAN CTD &country specific formats
  • Documents for Company registrations
  • Review, evaluation and Gap Analysis for compiled dossiers
  • Life cycle management