Murat Karadeniz

Role
Associate Director, Regulatory Affairs Cmc at Sarepta Therapeutics
Location
Cambridge, MA, US
LinkedIn followers
500 followers

About Murat Karadeniz

Regulatory professional more than 15 years of industry experience in many aspects of…

Experience

  1. Associate Director, Regulatory Affairs Cmc

    Sarepta Therapeutics

    Jun 2020 — Present

Skills

  • Gxp
  • Quality Assurance
  • Pma
  • Clinical Development
  • Change Control
  • Hplc
  • Cmc Regulatory Affairs
  • Drug Development
  • Design Control
  • Quality System
  • Gmp
  • Biopharmaceuticals
  • Regulatory Requirements
  • Fda
  • Nda
  • Clinical Trials
  • Lifesciences
  • Regulatory Affairs
  • Chromatography
  • CRO
  • Ce Marking
  • Pharmaceutical Industry
  • Glp
  • Ectd
  • Sop
  • Orphan Drugs
  • Medical Devices
  • Pharmacovigilance
  • Technology Transfer
  • Iso 13485
  • V&V
  • Gcp
  • Ind
  • Quality Control
  • Biotechnology
  • Computer System Validation
  • Pharmaceutics
  • Vaccines
  • Immunology
  • Regulatory Submissions

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Murat Karadeniz — Associate Director, Regulatory Affairs Cmc at Sarepta Therapeutics in Cambridge, MA, US | Unifers