2-day In-person Seminar on “Validations and Resolving Problems Related to Them” at Mumbai

Overview:
This course is designed for people who are growing in their knowledge of pharmaceutical industry practices and regulations. It will be a "how to" course where the instructors will explain the reasoning as well as the procedures that should be used to meet the various requirements of pharmaceutical regulations as they are applied to validations. The instructors will present different areas of study and present them 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 they will explain how pharmaceutical regulatory requirements can be met when conducting the work. Each instructor has decades of experience in working with and within the regulated pharmaceutical industry in the US. They will be covering topics that they are familiar with and will present them in a manner aimed at workers who may have been introduced to basic pharmaceutical practices and regulations, and now wish to expand their knowledge base. 

Why should you attend?
Any pharmaceutical worker, who performs, supervises or reviews development and manufacturing processes needs to develop a full understanding of the regulations and their ramifications. This is particularly true for workers in Regulatory Affairs, Quality Control and Quality Assurance as many of the required studies and their documentation will be assigned to them. All workers who supervise or execute development and manufacturing processes should have a firm understanding of pharmaceutical regulatory subjects as these will become a routine part of pharmaceutical development and manufacturing for all types of medicinal products, and must become a part of the body of knowledge possessed by senior workers. 

Who Will Benefit:

1. Directors
2. Managers
3. Supervisors, and lead workers in Product and Process Development
4. Manufacturing
5. Regulatory Affairs
6. Quality Assurance and Quality Control
7. Workers who will be participating in operations or the supervision of the development
8. Manufacturing or testing of medicinal products will benefit from knowing the procedures and applications of various areas of pharmaceutical regulations.

Speaker Profile:

Dr. 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. 

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 biological through all phases of clinical research and final product production.

Date, Venue and Price:

Held from November 11th - 12th, 2013

Hotel: The Lalit Hotel
Address: Sahar Airport Road, Andheri East, Mumbai - 400059 

Price: 18,000.

Contact Information:
Event Coordinator

Toll free:  +91 80-3247-3694, +91 80-3201-4957

Fax:  302 288 6884

Email:  customersupport@globalcompliancepanel.com  

Website:  https://www.globalcompliancepanel.in

GlobalCompliancePanel

NetZealous Services India Pvt. Ltd.

Gururaya Mansion, 759 to 764, 8^th Main Road, J.P.Nagar, Bangalore - 560070.  INDIA.

Seminar Link: http://bit.ly/16E9zLG