ComplianceOnline

Importance of Method Validation Protocols and components of MVP in the Laboratory

Instructor: Brian Jones
Product ID: 701689
  • Duration: 27 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Oct-2010

Training CD / USB Drive

$450.00
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CD/USB and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

Learn method validation protocol components and how to include MVPs in your lab performance testing.

Why Should You Attend:

Method Validation Protocols show that you are doing what you say you are doing - as long as you document, document, document and report the data you have obtained.Method Validation Protocols (MVP's) are more than just necessary in the laboratory performing testing. This presentation will show what to include in your Method Validation Protocol, how to include it, and example acceptance criteria. This is your license to operate. Developing a stability indicating method is important. Use the FDA Guidances to be ready for what is expected.

Areas Covered in the Seminar:

  • Background of Method Validation.
  • Importance of Method Validation .
  • What are FDA and Global Requirements?
  • What are stability indicating methods?
  • What is intermediate precision?
  • Document the Process.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in: Pharmaceutical, Biotechnology, Ros and Research Facilities Conducting Clinical Trials including:

  • Laboratory Managers
  • Laboratory Section Heads
  • Senior Scientists
  • Quality Assurance Managers and auditors
  • Regulatory Compliance Associates and Managers

Instructor Profile

Brian Jones, has over fifteen years experience in the pharmaceutical industry in many different capacities. As a research scientist, worked with the Analytical Development Department to improve the test methods being developed. And wrote and reviewed departmental procedures and technical reports. As a Quality Control chemist, performed qualitative and quantitative chemical and physical testing as specified by standardized procedures.

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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 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@complianceonline.com call +1-888-717-2436 (Toll Free).

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