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Webinar On "Assess Your Laboratory - Based on the FDA System Based Inspections"

Event Details

Webinar On "Assess Your Laboratory - Based on the FDA System Based Inspections"

Time: June 26, 2018 from 1pm to 2:30pm
Location: Online
Street: 9106 Seven Locks Road
City/Town: Bethesda
Website or Map: http://www.compliancetraining…
Phone: 1-844-216-5230
Event Type: online, /, webinar
Organized By: Sam Miller
Latest Activity: Jun 13

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Event Description

Description :

The Quality Control Laboratory plays an important part role in the production and release of a drug product regulated by the FDA. Inspectional observations of non-compliant laboratory operations are high on the list of most frequent regulatory observations. As the industry focuses more on the quality system and product and test method lifecycle, the operation of the laboratory unit becomes more visible. The laboratory should have active programs in which the laboratory is routinely assessed for compliance to applicable regulations and standards.

Areas Covered in the Session :

Standards for the assessment of laboratories
FDA System based inspection
The audit process – what to look for
The audit report
Audit follow-up

Who Will Benefit:

Method Development laboratory managers
Quality Control laboratory managers
Quality Assurance Managers
Analytical
Method Development chemists
Quality Control chemists
Internal auditors

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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