GMP Audits: Tools and Techniques

Duration: 60 Minutes
flat 50% off on this webinar
This webinar will provide the tools and techniques used during a GMP Audit. It will cover the basic requirements for a GMP Audit and will provide the information needed to successfully conduct an audit.
Pharmaceutical GMP regulations
Instructor: Carl Patterson
Product ID: 509664
Objectives of the Presentation
  • Understand the GMP context for pharmaceutical quality system lead auditors
  • Plan, conduct, report and follow-up an audit of a GMP PQS
  • Provide guidance for auditors of suppliers, contractors, CMO service providers, outsourced activities and self-inspectors
  • Drive continuous improvement of systems and processes
  • Drive continuous improvement of auditors and audit systems
Why Should you Attend
Because of the extreme criticality of GMP audits and the potential consequences, many pharmaceutical manufacturers have adopted a program of internal and external GMP audits in order to find and correct areas where sites are not in full compliance with the GMP regulations before an FDA audit occurs. By providing proper tools and techniques to be used during a GMP audit, the auditor can begin to understand the areas where improvements are needed.

This webinar will provide you with the knowledge, understanding, skills and confidence to audit all aspects of pharmaceutical manufacture and control, whilst retaining the cooperation and respect of the other personnel.

Areas Covered
Principles and Audit Planning
  • Planning and preparation
  • Audit types and techniques
  • Internal vs. external audits
  • The audit process
Auditor Skills and Competencies
  • What makes a good auditor
  • Managing audits
Initiating, Preparing and Conducting the Audit
  • Materials management
  • Documentation systems
  • Pharmaceutical quality systems
Who will Benefit
This webinar will provide valuable assistance to the following personnel in pharma, biopharma and food manufacturing companies:
  • Quality Assurance
  • Quality Control
  • Production
  • Logistics
  • Manufacturing
  • Quality system auditors
  • QA directors and managers
  • Consultants
  • Regulatory and Compliance Management
$375
Recorded Session for one participant
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How it works
Live Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Carl Patterson, M.S. has completed twelve plus years in the biotechnology, pharmaceutical manufacturing and quality fields. He completed his Bachelor's of Science in Microbiology from the University of Texas. Also, has completed specialized certificates in biotechnology manufacturing, quality control, and quality assurance from UCSD, and has completed his Master's of Science in Biomedical Quality Systems from SDSU. Through the years, has worked with several companies in regards to aseptic processing and has helped to insure the expectations, related to aseptic processing, have been met.
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