Seminar on GMP Compliance for Pharmaceutical Quality Control Laboratories at Singapore

Overview:

This course will present the regulations and guidelines that apply to operations in quality control testing laboratories. In some cases these will not be specific regulations, but needs that, if met, will increase the efficiency or quality of activities in the laboratory. While it will not be possible to cover all of the subtle variations among regulatory regions, general internationally accepted practices that comply with GMP requirements will be covered.

Why should you attend?

Since quality control is recognized as a manufacturing function, any pharmaceutical worker who deals with the manufacture of products should attend this course in order to gain an understanding of the regulatory requirements that apply to the testing and interpretation of test results as they relate to the monitoring and release of pharmaceutical products. In particular workers in and supervisors of pharmaceutical quality control laboratories will find this course to be of interest. In addition, workers in regulatory affairs and quality assurance will benefit as they will need to understand general GMP requirements when assessing the quality of product lots and presenting test results and process monitoring data to regulatory agencies.

Who will benefit:

Directors

Managers

Supervisors, and lead workers in Manufacturing, Quality Control, Regulatory Affairs, and Quality Assurance

Workers who will be participating in operations or the supervision of Quality Control testing or the interpretation of test results.

Speaker

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.

Price:

Register now and save $200. (Early Bird) Until August 20, Early Bird Price: $1,695.00 from August 21 to September 19, Regular Price: $1,895.00

Venue: Mandarin Orchard Singapore

Hotel Address: Mandarin Orchard Singapore   333 Orchard Road, Singapore 238867

Date & Time:

September 21st & 22nd, 2015

Time: 9:00 AM to 6:00 PM

Contact Information:

NetZealous LLC,

DBA GlobalCompliancePanel

161 Mission Falls Lane,

Suite 216, Fremont, CA 94539, USA         

USA Phone: 800-447-9407

Fax: 302-288-6884

support@globalcompliancepanel.com  

http://www.globalcompliancepanel.com