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Clinical Medical Director & Quality Control Specialist

Gregory Jean-NoelMD, MBA

Physician who has overseen projects from product development through FDA submission and provides risk assessments on complaints and early development.

  • Quality Control
  • Risk Assessment
  • Clinical
  • DEA

Many years of pharmaceutical industry experience

Background

Gregory Jean-Noel, MD, MBA has many years of pharmaceutical industry experience monitoring quality control, responding to medical inquiries from patients and pharmacists, participating in research and development activities, and responding to FDA regulatory inquiries and investigations.

He has held positions as Clinical Medical Director and Project Manager, responsible for overseeing projects from product development through FDA submission. Gregory also provides risk assessments regarding complaints and early developmental activities. He is a certified designated representative with extensive knowledge of federal GMP and DEA regulations.

What Gregory does on an engagement

  • Quality control monitoring and oversight
  • Complaint and early-development risk assessment
  • Medical inquiry and Agency response support
  • Project oversight from development through submission

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Describe the product, the process or the problem. We will tell you honestly whether we are the right people to help, and who should be on the team if we are.

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