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)

	Mail : anshuman.panda@cutm.ac.in
	Location : Paralakhemundi