Prof Anshuman Panda

  • Experienced regulatory affairs professional with 12+ years of experience in the pharmaceutical industry.
  • Proven track record of success in managing and executing regulatory submissions to global regulatory agencies, including the US FDA, EMA, and MHRA.
  • Expertise in all aspects of regulatory affairs, including product development, clinical trials, and post-market surveillance.
  • Strong communication and interpersonal skills.
  • Ability to work independently and as part of a team.
Skills
  • Regulatory Submissions: US FDA, EMA, MHRA, WHO
  • Product Development: CMC, CTD, IND, NDA
  • Clinical Trials: GCP, ICH-GCP
  • Post-Market Surveillance: pharmacovigilance, risk management
  • Regulatory Compliance: ISO 13485, GMP
  • Documentation: SOPs, protocols, reports
  • Communication: oral, written, presentation
  • Interpersonal: teamwork, conflict resolution
Education
  • Master of Pharmacy (Pharmaceutics) from; Rajiv Gandhi University of Health Sciences, Bangalore, India
  • Bachelor of Pharmacy (Pharmaceutical Sciences) from; Roland Institute of Pharmaceutical Sciences (Berhampur University), Odisha, India.
Experience Regulatory Affairs & R&D
  • Macleods Pharmaceuticals Ltd, India (2007 - 2008)
  • IPCA Laboratories Ltd, India (2008-2010)
  • Cipla Ltd., (2010-2011)
  • Teva Pharmaceuticals Ltd., (2011-2015)
  • Parexel International Ltd., (2015-2019)
Academics
  • Centurion University of Technology and Management (2022-Present)
Any review founded
COURSE
PRICE

Good Manufacturing Practices

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Quality Assurance & Quality Control of Herbal Products

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Regulations & Certifications of Herbal Drugs

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Mail : [email protected]

Location : Paralakhemundi

Contact Me