Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

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Monday, May 16th at 9:00am PST - Tuesday, May 17th, 2022

Online sale ends: 05/16/22 at 8:30am PST

Virtual Seminar

6201 America Center Drive Suite 240, San Jose, CA 95002, USA

San Jose, CA 95002

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Description

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.

Presented By

Time

9:00am to 3:00pm
Doors open at 9:00am

Price

General Admission: $1,299.00

Venue

Virtual Seminar<br> 6201 America Center Drive Suite 240, San Jose, CA 95002, USA<br> San Jose, 95002

Info Line

+1-888-717-2436