Time: June 25, 2018 at 9am to June 26, 2018 at 6pm
Location: WILL BE ANNOUNCED SOON
Street: WILL BE ANNOUNCED SOON
Website or Map: https://www.globalcompliancep…
Event Type: seminar
Organized By: John Robinson
Latest Activity: Apr 26, 2018
Course "FDA Trends for Computer System Validation (CSV) Compliance and Enforcement" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
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 seminar will help you understand the FDA's current thinking on computer systems that are validated and subject to inspection and audit.
As a "GxP" system following Good Manufacturing, Laboratory and Clinical Practices; the computer system must be validated in accordance with FDA requirements. If electronic records and/or electronic signatures (ER/ES) are incorporated into the system, FDA's CFR Part 11 guidance on ER/ES must be followed.
Location: Boston, MA Date: June 25th & 26th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON
Price: $1,295.00 (Seminar Fee for One Delegate)
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*
Register now and save $200. (Early Bird)
Until May 10, Early Bird Price: $1,295.00 From May 11 to June 19, Regular Price: $1,495.00
Sponsorship Program benefits for “FDA Trends for CSV Compliance and Enforcement” seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
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