Seminar on Modern Approaches to Process Validation
| Date: | 10-Dec-15 to 11-Dec-15 |
| Location: | Hilton Copenhagen Airport / Copenhagen / Denmark |
| Category: | Education |
Overview:
Companies face many common issues and confusion when creating or revamping their validation programs. Some of these common issues are:
• Company has expertise in its process validation program but can never quite get is arms around the facility and equipment changes that require never ending equipment qualification (IQ, OQ, PQ),
• Customer or 483 audit findings require the company to deviate from its own validation program to meet the needs of the FDA or the customer
• For systems that employ software and hardware, how does the company manage the validation activities (i.e. through the software validation effort or through the equipment qualification program?
Well, the answers to these and many, many more typical questions are now available in this simple to understand, yet detailed training session designed to help manufacturers of FDA regulated products build (or rebuild) a sustainable validation program.
Location: Copenhagen, Denmark
Venue: Hilton Copenhagen Airport
Venue Address: Ellehammersvej 20, Copenhagen, 2770
Date: December 10th & 11th, 2015, Time: 9:00 AM to 6:00 PM
Price: $1,695.00 (Seminar for One Delegate - Without Stay)
&
Price: $2,095.00 (Seminar for One Delegate - With Stay)
Register now and save $200. (Early Bird)
Until November 22, Early Bird Price: $1,695.00 from November 23 to December 08, Regular Price: $1,895.00
Until November 22, Early Bird Price: $2,095.00 from November 23 to December 08, Regular Price: $2,295.00
Quick Contact:
NetZealous DBA as GlobalCompliancePanel
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.
Phone: 1-800-447-9407
Fax: 302-288-6884
Email: support@globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com
Registration Link - http://bit.ly/1QrgUT2
Companies face many common issues and confusion when creating or revamping their validation programs. Some of these common issues are:
• Company has expertise in its process validation program but can never quite get is arms around the facility and equipment changes that require never ending equipment qualification (IQ, OQ, PQ),
• Customer or 483 audit findings require the company to deviate from its own validation program to meet the needs of the FDA or the customer
• For systems that employ software and hardware, how does the company manage the validation activities (i.e. through the software validation effort or through the equipment qualification program?
Well, the answers to these and many, many more typical questions are now available in this simple to understand, yet detailed training session designed to help manufacturers of FDA regulated products build (or rebuild) a sustainable validation program.
Location: Copenhagen, Denmark
Venue: Hilton Copenhagen Airport
Venue Address: Ellehammersvej 20, Copenhagen, 2770
Date: December 10th & 11th, 2015, Time: 9:00 AM to 6:00 PM
Price: $1,695.00 (Seminar for One Delegate - Without Stay)
&
Price: $2,095.00 (Seminar for One Delegate - With Stay)
Register now and save $200. (Early Bird)
Until November 22, Early Bird Price: $1,695.00 from November 23 to December 08, Regular Price: $1,895.00
Until November 22, Early Bird Price: $2,095.00 from November 23 to December 08, Regular Price: $2,295.00
Quick Contact:
NetZealous DBA as GlobalCompliancePanel
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.
Phone: 1-800-447-9407
Fax: 302-288-6884
Email: support@globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com
Registration Link - http://bit.ly/1QrgUT2
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