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CfPIE Announces Advisory Board to Support Continued Life Sciences Training Alignment with Industry Regulations
Date:3/27/2013

Malvern, PA (PRWEB) March 27, 2013

The Center for Professional Innovation and Education (CfPIE), announced today that is has formed an advisory board to support the following mission: to help life science professionals stay compliant with worldwide regulatory requirements through expert guidance, high quality training, and certification programs.

The advisory board is comprised of six CfPIE course directors:

  • Michael A. Pierro, a consultant leveraging 35 years of pharmaceutical industry experience to guide SOPs, study management/monitoring, auditing, and site qualification. His former roles within Sanofi-Aventis assisted the company with maintaining regulatory compliance.
  • John Geigert, Ph.D. assisted IDEC Pharmaceuticals, Immunex Corporation, and Cetus Corporation obtain regulatory approvals for six biopharmaceutical products, now commercially available, during his 35 years in biopharmaceutical and CMC industries.
  • Janet Gough has extensive experience as a consultant to the pharmaceutical, biotechnology, and medical device industries. Her specialties lie in medical and technical writing, SOPs, R&D reports, regulatory submissions, and document management.
  • Bill Hall, Ph.D., over the course of several decades in the pharmaceutical industry, held positions within a division of GlaxoSmithkline and the University of North Carolina at Chapel Hill. He specializes in validation, QA/QC regulations, stability programs, risk management, and GMP audits.
  • Byron Larson, a medical device consultant since 1986, formerly worked in R&D for Gambro. He specializes in design control, validation, and verification, risk analysis, medical combination products, and medical device submissions.
  • Kerry P
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