Scott Liebman

Scott Liebman

Partner I Chair of FDA Regulatory & Compliance I Co-Chair of Life Sciences Practice I Sheppard Mullin Richter & Hampton LLP

Role
Partner at Sheppard
Location
New York, NY, US
LinkedIn followers
500 followers

About Scott Liebman

I lead SMRH’s FDA Regulatory & Compliance and Life Sciences practices. I resolve compliance issues for pharmaceutical, medical device and biotechnology companies by delivering practical legal advice with sensitivity to business concerns. With technical understanding of FDA and state rules, I tailor guidance to meet state and federal mandates while advancing an organization’s healthcare mission. My experiences span the market with exposure to hundreds of life sciences corporations, from household-name manufacturers with thousands of sales representatives to virtual companies with fully outsourced functions.SpecialtiesFDA and state law issues, Food Drug & Cosmetic Act, Affordable Care Act, Anti-kickback issues, Off-label issues, OIG Guidance, Comprehensive compliance programs, PhRMA and AdvaMed codes, Promotional review, PDMA, Significant loss thresholds, Aggregate spend / transparency and disclosure laws, Distribution licenses, Compliance audits and risk assessments, Sales force and management training, Consultant and third-party contracts.

Experience

  1. Partner

    Sheppard

    Feb 2022 — Present · NY, US

Education

  • Seton Hall University School of Law

    JD

  • Lehigh University

    BA

Skills

  • Privacy Law
  • Legal Compliance
  • Regulatory Affairs
  • Lifesciences
  • Promotional Review
  • Licensing
  • Pharmaceutical Industry
  • Fda
  • Contract Negotiation
  • Oig
  • Aggregate Spend
  • Medical Compliance
  • Oig Guidance
  • Life Sciences
  • State Reporting
  • Off-Label
  • Compliance
  • Biotechnology
  • Regulatory Requirements
  • Pdma
  • Anti-Kickback Statute
  • Fcpa
  • Training
  • Pharmaceutical Law
  • Medical Device Law
  • Medical Devices
  • Federal Reporting
  • Healthcare
  • Risk Assessment

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