Essentials Of USP Microbiology - Reading Between the Lines of the USP General and Information Microbiology Chapters

The objective of this two day "Essentials of USP Microbiology" seminar is to explore USP General and General Information Chapters to learn which are available and to confirm that those that you are using are being used correctly. USP documents that will be reviewed include USP <51>, <61>, <62>, <71>, <1072>, <1111>, <1112>, <1113>, <1116> and others. Various team exercises will be conducted to allow the participants to use these USP documents to solve "real life" problems. Plan to bring a cross-functional group of your personnel to attend this invaluable two day seminar.

Learning Objectives:

The various General and General Information USP Chapters that apply to microbiology

The focus of the chapters to include those that primarily involve non-sterile and sterile applications

Chapters that involve the environment

Examining the changes within the various Chapters that have recently occurred and how to interpret them

Review areas that are often overlooked

Who Will Benefit:

Manufacturing

Product Development

Project Management

Quality Assurance

Quality Control

Topic Background:

Microbiology plays a role throughout the manufacture of pharmaceutical products. Whether the final product is non-sterile or sterile, the bioburden exists from the raw materials, throughout the process and/or within the product's environment (water and HVAC) to the final product.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2016.

For Registration:

http://www.complianceonline.com/usp-microbiology-chapters-general-and-information-microbiology-raw-material-api-hvac-ep-jp-seminar-training-80241SEM-prdsm?channel=sciencedz