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Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory

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This 2-hr laboratory inspection webinar will discuss strategies to implement before your laboratory is about to undergo a pre-approval inspection or a general GMP inspection. It will help you gain an understanding of the key areas that are likely to be the subject of a laboratory inspection.

Speaker
Instructor: Gregory Martin
Product ID: 702534
Training Level: Intermediate

Course "Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory" has been pre-approved by RAPS as eligible for up to 2 RAC credits towards a participant's RAC recertification upon full completion.

Why Should You Attend:

This laboratory inspection course is designed to provide participants with an understanding of the areas which are likely to be the subject of a laboratory inspection, whether it is a Pre-Approval Inspection or a general GMP inspection. By understanding the expectations, the participants will be able to develop a strategy to minimize issues should their laboratory be inspected.

Upon completion of this course the participant should:

  1. Be familiar with the areas in which regulatory inspectors are likely to probe.
  2. Be aware of the general expectations for each of these areas.
  3. Develop an overall strategy to minimize the likelihood of issues arising during an inspection.
Due to the diverse interests of the participants, questions will be actively solicited and addressed by the end of the webinar.

Areas Covered in this Webinar:

  1. Types of Inspections.
  2. Personnel Organization and Records.
  3. Instrument Inventory, Qualification and Change Control.
  4. Key SOPs Every Lab Should Have, and Related Training and Maintenance.
  5. Log of Out of Specification Results.
  6. Documentation of Analytical Procedures, including Validation, Verification and Change Control.
  7. Documentation of Analytical Data and Reports.
  8. Trending of Analytical Data, Laboratory Incidents and OOS Reports.
  9. Brief Introduction to Expectations for Computer Systems.
  10. Attendee Questions and Answers.

Who Will Benefit:

Instructor Profile:

Greg Martin, is President of Complectors Consulting which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. He has particular interest in QbD/Lean approaches to dissolution testing, impurity methods, method lifecycle (development/validation/transfer) and instrument qualification, and is passionate about using good science and sound logic to achieve high quality results, consistent with cGMPs, while minimizing resources. Mr. Martin has over 25 years experience in the pharmaceutical industry and was Director of Pharmaceutical Analytical Chemistry (R&D) for a major PhRMA company for a number of years. In addition, he has volunteered for the USP for over 10 years, and currently serves as Vice Chair of the General Chapters – Physical Analysis Expert Committee, and serves on Expert Panels on Validation and Verification, Weights and Balances and Use of Enzymes for Dissolution Testing of Gelatin Capsules. He is also Chair-elect of the AAPS In Vitro Release and Dissolution Testing Focus Group.

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Refund Policy
"Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance.
ComplianceOnline would process/provide refund only if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs."
For substitution, please email editor@complianceonline.com or call +1-650-620-3937.

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Training Options Training Duration = 120 Min
$399.00 Access Recorded Version Only
One Person - Unlimited viewing for 6 Months
(For multiple licenses contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
$499.00 Get Training CD Only
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days