Live In-Person Seminar on “GMP Compliance for Pharmaceutical Quality Control Laboratories” By Steven Kuwahara

Event Details

Time: September 11, 2014 at 9am to September 12, 2014 at 6pm
Location: Melbourne, Australia
Street: Melbourne, Australia
City/Town: Melbourne, Australia
Website or Map: http://bit.ly/WbQ8G8
Phone: 18004479407
Event Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
Organized By: GlobalCompliancePanel
Latest Activity: Aug 6, 2014

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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 laboratory within the regulated pharmaceutical industry in the US. He will be covering topics that he is familiar with and will present them in a manner aimed at workers who may have been introduced to basic QC practices and regulations, and now wish to expand their knowledge base.

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. This is particularly true for workers in Regulatory Affairs, Quality Control and Quality Assurance as many of the required activities and their documentation will be assigned to them either for performance or review.

Who will benefit:

Directors
Managers
Supervisors, and lead workers in Product and Process Development
Manufacturing
Regulatory Affairs
Quality Assurance and Quality Control

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. 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.

Date, Venue and Time:

Location: Melbourne, Australia

Date: September 11^th & 12^th 2014

Time: 9 pm to 6 pm

Venue: Will Be Announced Soon

Price: $1595.00 (Seminar for One Delegate)

Discount: Register now and save $200. (Early Bird)
Until August 15, Early Bird Price: $1,595.00

From August 16 to September 09, Regular Price: $1,795.00

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