Stability Program 2015 - Stability Program

This training on pharmaceutical stability studies will highlight the key factors that would affect the shipping and distribution of drug products. It will explain the stability studies that need to be done to support shipping and distribution of drugs.
Why Should You Attend:
A drug product must maintain its identity, strength, quality and purity till its expiration. Physical, chemical and biological data are influenced by various environmental factors such as temperature, humidity and light. In current manufacturing environment, products can be shipped and distributed across different climatic zones. Seasonal changes as well as types of transportation can greatly affect the supply chain of the products.
This webinar will outline stability studies to support shipping and distribution of drug products. On completing this session, attendees will learn key factors that would affect the shipping and distribution of drug products. Participants will understand product stability profile, typical environmental conditions for storage, and anticipating environmental extremes for distribution. This information will be necessary to design shipping conditions in order to maintain quality of the drug product till expiry.
Areas Covered in the Webinar:
Goal of stability studies.
Warning letters and observations on shipping and distribution practices.
Short term excursion study.
Thermal cycling study.
Analytical testing for these studies.
Who Will Benefit:
Pharmaceutical scientists
Manufacturers of raw material and ingredients
Analysts and lab managers
QA managers and personnel
Regulatory affairs personnel
For Registration:http://www.complianceonline.com/stability-program-...