- Understand the specific requirements associated with local and SaaS/cloud hosting solutions.
- Nearly every computerized system used in laboratory, clinical,
manufacturing settings and in the quality process has to be validated.
Participants learn how to decrease software implementation times and
lower costs using a 10-step risk-based approach to computer system
validation.
- The instructor reviews recent FDA inspection trends and discusses
how to streamline document authoring, revision, review, and approval.
- Participants will learn how to write a Data Privacy Statement to comply with the EU General Data Protection Regulation (GDPR).
- This course benefits anyone that uses computer systems to perform
their job functions and is ideal for professionals working in the health
care, clinical trial, biopharmaceutical, and medical device sectors. It
is essential for software vendors, auditors, and quality staff involved
in GxP applications.
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Presented By
9:00am to 3:00pm
Doors open at 9:00am
General Admission: $1,299.00
Virtual Seminar<br> 6201 America Center Drive Suite 240, San Jose, CA 95002, USA<br> San Jose, 95002
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Thursday, April 21st
Virtual Seminar
Past Event
Monday, April 18th
Virtual Seminar
Past Event
Monday, April 11th
Virtual Seminar
Past Event
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