Responding to Compounding Pharmacy Inspections

Wednesday, Jan. 25, 2017 · 1:30 p.m. - 3:00 p.m. EST

The FDA is looking to shed light on the sometimes murky rules governing compounding  operations primarily regulated on the state level, only adhering to USP 797 Pharmaceutical Compounding — Sterile Preparations.

In April 2016 the agency released three draft guidances addressing multiple facets of the compounding industry including: what constitutes a large-scale compounding facility… associated GMP requirements… standards for hospital compounding… and requirements for compounding without a prescription.

All three guidances emphasize that all products manufactured by outsourcing facilities must comply with GMP rules or be deemed in violation.

If you want to know how these guidances might affect your company, plan on attending Responding to Compounding Pharmacy Inspections. This 90-minute webinar will:

  • Identify the latest areas of FDA enforcement in compounding pharmacies
  • Compare requirements of 503A (traditional compounder) and 503B (outsourcing facility)
  • Review USP 797 vs. GMP requirements
  • Identify the constitution of your core FDA Inspection Team
  • Allow you to create the outline of an appropriate FDA response

Register today and be informed about compounding facility inspections.

Who Will Benefit

  • Pharmacists
  • Compliance officers
  • Quality Managers
  • Regulatory Affairs
  • General/corporate counsel
  • Executive management
  • Quality assurance
  • Risk management specialists
  • Outside attorneys
  • Regulatory/legislative affairs professionals
  • Department supervisors/directors

Webinar plus Audio CD/Transcript
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$487

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Webinar only
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$287

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24/7 Encore plus CD/Transcript
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$487

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24/7 Encore Presentation
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$287

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Audio CD/Transcript
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$287

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Meet Your Presenter

Darshan Kulkarni

Principal Attorney
Kulkarni Law Firm

Darshan Kulkarni of the Kulkarni Law Firm is a leading expert on strategic regulatory and pharmaceutical counseling. With a background in both the law and hands-on healthcare experience (over 10 years as a pharmacist, including participation as a clinician in clinical trials), Mr. Kulkarni is versed in the needs of international device, pharmaceutical and biopharmaceutical companies and their service providers, including contract manufacturing organizations and contract research organizations.

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA.

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