Webinars Details - Leveraging Supplier Involvement for Clinical and Safety System Validation
Webinars
Event
- Title:
- Leveraging Supplier Involvement for Clinical and Safety System Validation
- When:
- 08.20.2010
- Category:
- Clinical Automation
Description
Webinar Date: August 20, 2010 Time: 11:00 to 11:30 PST
Summary:
Most organizations struggle to contain the cost of validation while innovating business process through new technology deployment. GAMP 5 suggests organizations look to leverage supplier involvement as much as possible to avoid documentation and verification reinvention where possible. Conducting appropriate risk assessments of trusted suppliers will establish creditability and rational to incorporate existing documentation, product knowledge and expertise.
Please join USDM in exploring how to effectively lower the cost of Clinical and Safety System Validation though the use of product specific validation accelerator packs. Discussion highlights include:
- GAMP 5 says: Life Sciences organizations should maximize supplier involvement to leverage documentation, expertise and knowledge.
- How to rationalize the use of supplier documentation?
- Learn how product specific Validation Accelerator Packs reduce the upfront validation and downstream operational cost.
- Review contents of a Validation Accelerator Pack for Oracle Life Science Applications as an example.
Sponsored by the USDM Clinical Automation Practice Learn More
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About USDM
USDM is a leading global consulting firm focused on life sciences. We specialize in regulated business processes, with an emphasis on compliance and performance.
USDM provides innovative services and solutions that enable life science companies to achieve and maintain compliance across the entire enterprise.
