Auditing Analytical Laboratories for FDA Compliance 2017

Course "Auditing Analytical Laboratories for FDA Compliance" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:

Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

Who will benefit:

The following specific types of workers will benefit from this webinar:

• External and Internal Auditors
• Supervisors and Analysts in Quality Control Laboratories and Quality Assurance groups
• Supervisors and Analysts in Contract Testing Laboratories
• Personnel Responsible for Selecting Contract Testing Laboratories
• Consultants

 Location: Manila, Philippines Date:  November 20th & 21st, 2017 and Time: 9:00 AM to 6:00 PM

Venue:  WILL BE ANNOUNCED SOON, Manila, Philippines

Price:

Price: $895.00 (Seminar Fee for One Delegate)

Register for 5 attendees   Price: $2,685.00   $4,475.00 You Save: $1,790.00 (40%)*

Register now and save $200. (Early Bird)

Until October 10, Early Bird Price: $895.00 From October 11 to November 18, Regular Price: $1,095.00

Register for 10 attendees   Price: $4,922.00  $8,950.00 You Save: $4,028.00 (45%)*

Contact us today!

NetZealous LLC DBA GlobalCompliancePanel

john.robinson@globalcompliancepanel.com  

support@globalcompliancepanel.com 

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

Registration Link - http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901324SEMINAR?medtechiq-November-2017-SEO

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