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Home›Webinar›FDAnews Announces: Free Webinar on How to Standardize Your Lab Investigation Process June 9, 2022 | New

FDAnews Announces: Free Webinar on How to Standardize Your Lab Investigation Process June 9, 2022 | New

By Richard R. Sutton
June 2, 2022
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Easily document and manage the Lab Investigation results process.

FALLS CHURCH, Va., June 02, 2022 /PRNewswire-PRWeb/ — How to Standardize Your Laboratory Investigation Process

Increase efficiency and reduce risk with a consistent process

A free FDAnews webinar, sponsored by ETQ

Thursday, June 9, 20222:00 p.m.–3:00 p.m. EDT

https://info.fdanews.com/how-to-standardize-your-lab-investigation-process

Today, life science companies struggle to effectively manage non-compliant lab test results:

  • Inability to electronically manage and track Out-of-Spec (OOS) or Out-of-tend (OOT) investigation.
  • Unable to identify the risk of an OOS or OOT to determine if corrective or preventive actions are necessary.
  • Limited visibility of the impact on the quality of their product due to an OOS.

This can result in an overall negative impact on product quality and brand reputation, as well as an FDA 483 finding.

Webinar attendees will learn how to easily document and manage the Lab Investigation results process. The new ETQ Lab Investigation app is designed to provide a standard process that anyone can follow. It ensures that every investigation is consistent across regulated industries where laboratory investigations are conducted. It ensures that all laboratory test results are easily accessible and helps assess risk to determine if further action is needed, reducing the likelihood of poor quality products entering the market.

Register for this live webinar and learn how to:

  • Perform laboratory investigation to ensure that each investigation is completed in a consistent and timely manner
  • Perform additional testing or resampling activities to confirm initial results
  • Track the results of each investigation and identify trends for root cause analysis
  • Identify risks and reduce quality defects by initiating corrective or preventive action, or a nonconforming material report to resolve supplier issues

Webinar details

How to standardize your laboratory investigation process

Increase efficiency and reduce risk with a consistent process

A free FDAnews webinar, sponsored by ETQ

Thursday, June 9, 20222:00 p.m.–3:00 p.m. EDT

https://info.fdanews.com/how-to-standardize-your-lab-investigation-process

Tuition:

Free

Easy commands:

On line:https://info.fdanews.com/how-to-standardize-your-lab-investigation-process

By phone: 888.838.5578 or 703.538.7600

About FDAnews:

FDAnews is the premier provider of domestic and international regulatory, legislative and business news and information for executives in industries regulated by the US FDA and European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews’ print and electronic newsletters, books and conferences to stay compliant with international standards and complex and ever-changing FDA regulations.

Media Contact

Michael ButlerFDAnews, 703-538-7665, mbutler@fdanews.com

SOURCEFDA news

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