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Compliance Training Panel.

Compliance Training Panel provides Quality trainings through their world class platform which enables the clients to discuss with industry experts and to gain related information.

Compliance Training Panel has been established by professionals in the field of Quality, Compliance Auditing and Health Care, Education & Finance with an objective to create an ecosystem that will deliver quality training's on compliance of various regulatory and legal requirements.

We are a US based organization specializing in online trainings in the form of Webinars and Seminars.


CAPA, A Key Element of the Pharmaceutical Quality System
Description :
In this webinar we will discuss CAPA (Corrective Actions and Preventive Actions), what they are and why the FDA expects the industry to initiate and complete timely corrective and preventive actions. We will also discuss the CAPA System, the procedure or family of procedures that manage corrective actions and preventive actions from the observation of a deviation through the verification of the corrective or preventive action.
Objective of the webinar:
Objective of the webinar The objective of this webinar is to inform personnel in the pharmaceutical of the growing expectation that each organization have an effective system that defines process and responsibilities for the identification, recording and investigation of deviations, the recommendation and execution of corrective actions and demonstrating that the action effectively correct and/or prevent the deviation.
Areas Covered in the Session :
In this webinar we will discuss CAPA (Corrective Actions and Preventive Actions) , what they are and why the FDA expects the industry to initiate and complete corrective and preventive actions. We will also discuss the CAPA System, the procedure or family of procedures that manage corrective actions and preventive actions from the observation of a deviation through the verification of the corrective or preventive action.
Who Will Benefit:
Personnel in production, quality control, quality assurance, materials, and functions that support these, will benefit from an understanding an effective CAPA system – a system for identifying, logging, investigating, determining the cause of the deviation and correcting the current deviation and/or preventing future occurrences of the deviation.
About Speaker:
John G. (Jerry) Lanese is an independent consultant with a focus on Quality Systems and the components of an effective Quality System. He received a BA and MS from Middlebury College and a Ph.D. in Analytical Chemistry from the University of Michigan and began his career teaching Analytical Chemistry in a small liberal arts college. Dr. Lanese moved from the academic environment to the pharmaceutical industry where he has managed Analytical Research, Quality Control and Quality Assurance functions.

In 1994 Dr. Lanese formed his own company, The Lanese Group, and since that time he has been a consultant in the area of quality system and cGMP compliance and has audited and consulted with small and large medical device and pharmaceutical companies, including companies under FDA Consent Decree, API and excipient manufacturers, electronic firms and other manufacturing organizations.

Dr. Lanese focuses on training. He lectures throughout the world and presents training in all formats (lectures, seminars and webinars) on a variety of topics related to Quality Systems, GMPs, APIs, training, laboratory operations, calibration, change control, deviations and product reviews for clients and seminar, webinar and conference providers. Jerry is a member of the Editorial Board of the Journal of GXP Compliance.
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