Pharmaceuticals 2011 - The Hero of Manufacturing Contamination Control -- The Microbiology Lab
Date2011-12-01
Deadline2011-12-01
VenuePalo Alto, USA - United States
Keywordscontamination control training;preventing contamination in manufacturing;contamination prevention;preventing microbial contamination;CAPA procedures compliance
Topics/Call fo Papers
This webinar on Contamination Control will discuss, how the micro lab can be more effectively utilized to prevent or head off microbial contamination issues as well as effectively resolve problems like recurring micro failures, investigations, and ineffective CAPAs.
Why Should You Attend:
The Microbiology Lab must take leadership in contamination control support for production because it is the hub of the necessary technical expertise. This broad manufacturing support role covers many areas, including routine raw material and product testing, disinfectant/sanitant qualification, water and compressed gas testing, environmental monitoring, microbiological “awareness training” of production operators, etc. Perhaps their most difficult leadership role is in contamination control investigations where product is at risk, manufacturing may be at a standstill, and the pressure to resume operation with a quick (and possibly incorrect) fix is tremendous. In these situations, the microbiology lab can either gain or lose credibility in the eyes of manufacturing management depending on the timeliness of its success in discovering and resolving the problems.
Other CFPs
- 2012 International Conference on Advanced Manufacturing Technology and Systems
- Construction of the European Drug Master File (EDMF) for Regulatory Agencies
- FDA's DDMAC Compliance: Current Issues and Emerging Perspectives
- 2012 International Conference on Green Buildings and Optimization Design (GBOD 2012)
- Understanding ISO 14644-1: What is Required of Pharmaceutical Manufacturers
Last modified: 2011-09-29 17:31:13