Performing Effective Management Review of the Quality System

This webinar will teach you how to conduct an effective management review of the quality system which helps you understand how to plan and focus on right metrics and governed by an efficient process. Participants will also understand FDA policy regarding disclosure of management review information during inspections.

$1,299.00
Introducing
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One User Unlimited access to all recorded webinars for 6 Months

Recorded Version Only

(PPT + Recorded Streaming Link)

$249.00
1x Person - Unlimited viewing for 6 Months (For multiple locations contact Customer Care)
rec Recorded Link and Ref. material will be available in My Account Section
Last Recorded Date: Apr-2022

Download File Only

(PPT + Recorded Training File)

$349.00
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(For multiple locations contact Customer Care)
Downloadable link along with the materials will be emailed within 2 business days
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Why Should You Attend:

Under FDA regulations, Medical device companies are required to perform at least an annual review of the quality system. Pharmaceutical companies are not required but are "expected" to do so in the U.S., and are required under certain non-US countries’ regulations. In addition, guidance documents from the FDA and industry groups encourage management review.

Management review can be burdensome and difficult if not planned to focus on the right metrics, and governed by an efficient process. This webinar explores a successful approach to the performance of management review that yields a value added result and helps gain the buy-in of the executive level whose support is needed.

Learning Objectives:
  • Understand the purpose of management review
  • Understand the regulatory requirement for management review
  • Understand an effective process for conducting the review
  • Understand documentation requirements
  • Understand FDA policy regarding disclosure of management review information during inspections
Areas Covered in the Webinar:
  • Regulatory requirements for management review
  • Status of management review under US, European and Canadian GMP, US medical device QSR, and via ICH Guideline Q10
  • Purpose of management review
  • Process for an effective management review
  • Documenting management review meetings
  • FDA policy on access to management review documentation during inspections
Who Will Benefit:
  • Quality Assurance managers
  • Manufacturing managers
  • Laboratory managers
  • Regulatory Affairs managers
  • Senior level executives
Instructor Profile:
David L. Chesney David L. Chesney

Principal and General Manager, DL Chesney Consulting LLC

David L. Chesney is the Principal and General Manager of DL Chesney Consulting, LLC. His career includes 23 years with the FDA and over 21 years in GMP and GCP consulting worldwide. In his consulting practice, Mr. Chesney helps clients prevent quality and compliance problems through proactive assessment and planning, and when necessary, with remediation planning and health regulatory authority communications.

Until recently, he served as Vice President, Strategic Compliance Services for PAREXEL Consulting, a business unit of PAREXEL International LLC. Prior to joining PAREXEL Consulting in 1995, Mr. Chesney served 23 years with the FDA, where he advanced from Investigator to Supervisory Investigator and Director, Investigations Branch, working in the Boston, Seattle and Philadelphia District Offices. In 1991, he was appointed the District Director, FDA San Francisco District Office, where he served until joining PAREXEL in 1995. For 19 years, he led the Strategic Compliance Consulting group, and also personally provided regulatory enforcement related consulting services to the pharmaceutical, medical device and biologics industries, plus technical assistance to legal counsel in FDA regulatory matters. Mr. Chesney has a bachelor's degree and postgraduate credits in biology from California State University, Northridge and San Diego, and received a Certificate in Health Care Compliance from Seton Hall University School of Law.

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. FDATrainingAlert would process/provide refund 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. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@fdatrainingalert.com call +1-888-771-6965 (Toll Free).

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