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
Study issues that continue to exist between the USP, EP and JP
Examine the new regulatory attitude that is occurring with non-sterile products
What now constitutes a "specified" and “objectionable” microorganism
Explore Form FDA 483s and Warning Letters for microbiological applications
Who Will Benefit:
Manufacturing
Product Development
Project Management
Quality Assurance
Quality Control
Regulatory Affairs
Regulatory Compliance
Note:
Use coupon code NB5SQH8N and get 10% off on registration.
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