Auditing Analytical Laboratories for FDA Compliance 2017

Start Date : November 20, 2017
End Date : November 21, 2017
Time : 9:00 am to6:00 pm

Phone : 800-447-9407
Email : john.robinson@globalcompliancepanel.com

Description

 

 

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:

 

Agenda:

 

 

Day 1 Schedule

 

Lecture 1:

GMP Regulations that Apply to Analytical Laboratories

Lecture 2:

Reviewing Documentation

Lecture 3:

Advance Preparation for the Audit

Lecture 4:

Auditing Styles and Structures

Day 2 Schedule

 

Lecture 1:

Equipment and Laboratory Instrument Qualification

Lecture 2:

What to look for while doing a Walk-Through

Lecture 3:

Other Regulations and Standards, including ISO 17025

Lecture 4:

Following through on the Audit

 

 

Speaker

Dr. Steven Kuwahara

Founder & Principal, GXP Biotechnology, LLC

Dr. Steven Kuwahara, Ph.D. is the Founder and Principal of GXP BioTechnology LLC, a consulting firm that works in the areas covered by the GLP and GMP of drugs, biologics, and nutraceuticals. Steve has over 30 years of experience in supervising quality control laboratories, including an animal testing facility, and in performing GLP and GMP audits of internal and external testing laboratories. Steve has participated in the development of drugs and biologicals through all phases of clinical research and final product production.

               

 

 

 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%)*

 

Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar

At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry.

As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory-related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.

For More Informationhttps://www.globalcompliancepanel.com/control/sponsorship 

 

 

 

 

 

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Organized by

Organized by globalcompliancepanel

NetZealous DBA as GlobalCompliancePanel ,
NetZealous LLC-globalcompliancepanel, 161 Mission Falls Lane, Suite 216, Fremont,CA 94539, USA

Tel: Event Manager
Mobile: 800-447-9407
Email: john.robinson@globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com


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