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Webinar on - Latest Trends in FDA Compliance and Enforcement for Regulated Systems
Presented By Global Wizdom
Wednesday, March 4th at 1:00pm MST
Online sale ends: 03/04/20 at 2:30pm MST
Live - Webinar
Kellogg Center 26 West Dry Creek Circle, Suite 600
Littleton, CO 80120
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Description
Overview:
FDA requires that all computer systems used to produce, manage and report on “GxP” (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. This webinar will help you understand the FDA’s current thinking on computer systems that are validated and subject to inspection and audit.

Areas Covered in the Session:
•  Computer System Validation (CSV) and the System Development Life Cycle (SDLC) Methodology
•  “GxP” – Good Manufacturing, Laboratory and Clinical Practices
•  21 CFR Part 11, Electronic Records/Electronic Signatures (ER/ES)
•  Data Archival to ensure security, integrity and compliance
Additional Information
FDA regulatory requirements

Presented By

1:00pm to 3:00pm
Doors open at 11:30pm

General Admission: $159.00

Age
21+

Live - Webinar<br> Kellogg Center 26 West Dry Creek Circle, Suite 600<br> Littleton, 80120

100

866-896-1646

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