Sanjeev Parida

Regulatory Affairs (Global submissions) at Novartis Healthcare Pvt. Limited

Role
Manager - Regulatory Affairs (Global Submissions) at Novartis
Location
Hyderabad, TG, IN
LinkedIn followers
500 followers
General Business & ManagementView LinkedIn profile

About Sanjeev Parida

Competent, diligent & efficient regulatory professional with more than 2 decades of…

Experience

  1. Manager - Regulatory Affairs (Global Submissions)

    Novartis

    Apr 2015 — Present · Hyderabad, IN

Education

  • Roland Institute of Pharmaceutical Sciences

    Bachelor of Pharmacy, Pharmaceutical Sciences

    1996 — 2000

  • Annamalai University

    M.Pharm, Industrial Pharmacy

    2001 — 2003

Skills

  • Regulatory Affairs
  • Cleaning Validation
  • Capa
  • Cmc
  • Ich Guidelines
  • Quality Assurance
  • Formulation
  • Pharmaceutical Industry
  • Sop
  • Fda
  • Generic Programming
  • Standard Operating Procedure (Sop)
  • Validation
  • Technology Transfer
  • Regulatory Submissions
  • Pharmaceutics
  • Anda
  • Ctd
  • Quality System
  • Ich-Gcp
  • Clinical Trials
  • Regulatory Filings
  • Cmc Regulatory Affairs
  • Ind/Impd
  • Drug Delivery
  • Glp
  • Maa
  • Gmp
  • Abbreviated New Drug Application (Anda)
  • Regulatory Requirements
  • Ind

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Sanjeev Parida — Manager - Regulatory Affairs (Global Submissions) at Novartis in Hyderabad, TG, IN | Unifers