India Seminar 2013 on “Good Laboratory Practice Regulations - Introduction and Strategies for Implementation” at Mumbai

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GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, “Good Laboratory Practice Regulations –Introduction and Strategies for Implementation” on March 21 and 22 at Mumbai, India.

Mumbai, Maharastra, India., February 18 2013 - (PressReleasePoint) -

Course Agenda:
Safety testing of medical productsis bound by a myriad of regulations and guidelines. Several rules apply to testing laboratories that study samples derived from test animals or test subjects in clinical studies, too. This two-day course will give participants a detailed understanding of these.

Obviously, laboratory personnel need to have deep and thorough knowledge of the material they test. If any material has to pass an FDA inspection; it has to meet stringent regulatory requirements, for which the basis is good knowledge of the material being tested. This course will help such personnel get an in-depth understanding of the nature of the material they test. The expert, Dr. Kuwahara, will also discuss the types of studies that come under the GLP regulations in detail.
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Purpose of the seminar
This seminar is designed to help any pharmaceutical worker who performs, supervises or reviews non-clinical studies related to product safety, get a clearer understanding of regulatory requirements set out by the FDA. Workers who perform studies on samples derived from animals or clinical subjects too, are required to know the ins and outs of testing regulatory requirements.
This course will be immensely useful to these kinds of professionals. It is a tool toward facilitating such professionals in gettinga good understanding of these requirements.
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About the Speaker:
Steven S. 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. After securing degrees in Biochemistry from Cornell and the University of Wisconsin, Steven started off as an Assistant Professor of Chemistry. His testing skills were honed in the initial years of his career at the Division of Biologic Products at the Michigan Department of Public Health (now BioPort Corp.), where he became the head of Quality Control. Here, he developed expertise in the testing of blood derivatives, viral and bacterial vaccines.
His work has also dealt with all aspects of GMP and GLP in relation to biopharmaceuticals. He has worked with small molecules, proteins, cells, and gene therapy vectors.

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Who will benefit:
a.       Directors
b.      Managers
c.       Supervisors
d.      Lead workers in Product Development
e.       Regulatory Affairs
f.        Quality Assurance and Quality Control
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DATE AND VENUE:
March 21 and 22, 2013
Venue: The Lalit Hotel Sahar Airport, Andheri East.
from 9 am to 6 pm EST at The Lalit Mumbai.
 Price –INR 18,000 per delegate for registrations made up to February 15.