MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

GMP Compliance for Pharmaceutical Quality Control Laboratories: 2-day In-person Seminar

Event Details

GMP Compliance for Pharmaceutical Quality Control Laboratories: 2-day In-person Seminar

Time: September 15, 2014 at 9am to September 16, 2014 at 6pm
Location: w hong kong
Street: 1 Austin Road West, Kowloon Station, Kowloon Hong Kong China
City/Town: Chicago
Website or Map: http://bit.ly/1tGT6Rr
Phone: 18004479407
Event Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
Organized By: GlobalCompliancePanel
Latest Activity: Aug 6, 2014

Export to Outlook or iCal (.ics)

Event Description

Overview:

This course is designed for people who are growing in their knowledge of pharmaceutical quality control practices and regulations. It will be a "how to" course where the instructor will explain the reasoning as well as the procedures that should be used to meet the various requirements of the pharmaceutical QC laboratory. The instructor will present different areas of work with a "how to" approach so that the seminar participant can see how the subject matter applies to the participant's work either now or in the future. In addition to discussing the particular subjects he will explain how pharmaceutical regulatory requirements can be met when conducting the work. The instructor has decades of experience in working with a pharmaceutical QC 

Why should you attend?

Any pharmaceutical worker, who performs, supervises or reviews development, validation, or manufacturing processes needs to develop an understanding of the operations of a QC laboratory. 

Who will benefit:

  • Directors
  • Managers
  • Supervisors, and lead workers in Product and Process Development
  • Manufacturing
  • Regulatory Affairs
  • Quality Assurance and Quality Control
  • Quality Control workers who will be participating in operations or the supervision of the development
  • Manufacturing, or testing of medicinal products will benefit from knowing the procedures and applications applicable to the quality control laboratory

 

Meet your Expert:

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. 

Date, Venue and Time:

Location: Hong Kong

Date:  September 15th & 16th, 2014

Time: Time: 9:00 AM to 6:00 PM

Venue: w hong kong

Venue Address: 1 Austin Road West, Kowloon Station, Kowloon Hong Kong China

Price: $1,195.00 (Seminar for One Delegate)

 

Discount: Register now and save $200. (Early Bird)
Until August 15, Early Bird Price: $1,195.00

From August 16 to September 13, Regular Price: $1,395.00

 

Want to register by Wire Transfer?

Please call any of our representatives on 1800 447 9407 to help you completed the transfer.

Contact Information:

John Robinson

Toll free: 1800-447-9407

Fax: 302-288-6884

Email: support@globalcompliancepanel.com

Website: https://www.globalcompliancepanel.com

Live Chat - Online Help Desk: http://www.globalcompliancepanel.com/chat/client.php

GlobalCompliancePanel

NetZealous LLC 

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA

For More Info on This Seminar Kindly Go through the Link: http://bit.ly/1tGT6Rr

Comment Wall

Comment

RSVP for GMP Compliance for Pharmaceutical Quality Control Laboratories: 2-day In-person Seminar to add comments!

Join MedTech I.Q.

Attending (1)

© 2020   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service