Data Integrity and Compliance with GxP It's not new and so much more than just computers

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Medical Devices Webinar Image
Date
16 October, 2019 (Wednesday)
Time
10:00 AM PST | 01:00 PM EST
Duration
75 Minutes

Overview

Discussion of requirements for operational excellence to ensure data integrity. Presentation includes major regulations and key operational requirements for systems that ensure data generated whether in paper or electronic form maintain their integrity and reliability throughout their lifecycle. 

Area Covered

Regulations and guidance - US, EU, MHRA, PIC/s; Regulatory Enforcement – Recent Examples; Infrastructure Requirements ; Pragmatic approaches

Why Should You Attend

Regulatory Agencies have been placing an increased emphasis on enforcement of data integrity. Too often companies have approached this increased enforcement as the regulators are enforcing new regulations and the issues are associated only with the laboratory.

Who Will Benefit?

All members of quality organizations from VP to front line operations; Members of senior management responsible for establishing and enforcing data integrity policies, procedures and controls.

Speaker

  • David Husman has over 30 years of diverse international industry experience in Quality Assurance, Quality Control, and Regulatory Affairs. He has worked for last 18 years as a consultant to biopharma, pharma, and device industries.
  • David's experience has spanned from R&D to Commercial Manufacture.
  • His background includes, but not limited to, parenteral products, human tissue products, blood products, biotech products, solid dosage, vaccines, implantable devices, and in vitro diagnostic products for both human and animal species.
  • His extensive experience in laboratory operations includes but not limited to auditing, development of laboratory system procedures, implementation of laboratory at a new site and forensic data integrity investigations.
  • He has experience in all parts of the manufacturing operation from warehousing to packaging, from facilities and utilities to laboratories to computer systems, from regulatory to quality control. 
  • He has an expert level knowledge in Compliance and Quality System development.
  • He has executed numerous Data Integrity assessments and remediation projects worldwide.
  • He is also a Ph.D. in Biochemistry, and is certified as a GMP expert and in Regulatory Affairs.

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