Print Page   |   Contact Us   |   Sign In   |   Join
Quality Audits in the (Bio)Pharmaceutical and Device Industry
Tell a Friend About This EventTell a Friend
 

 Export to Your Calendar 3/3/2017
When: 03/03/2017
10:00 am - 12:00 pm
Where: Biotility at UF CERHB
13706 Innovation Drive
Alachua, Florida  32615
United States
Contact: Tamara Mandell
386.432.6397

« Go to Upcoming Event List  

Quality Audits in the (Bio)Pharmaceutical and Device Industry

External and Internal Quality Audits in GMP manufacturing including the (bio)pharmaceutical and medical device industries are global regulatory compliance tools to ensure the safety and effectiveness of drugs, vaccines, other biological products, and devices. The course includes an overview of regulatory requirements, the different types of audits, and how to prepare for, conduct, and follow up on an audit. Special attention will be given to the internal audit which is a company’s most important managerial tool for monitoring the quality of processes and products. Internal audits, when effectively implemented, are critical to the identification of weaknesses and the continual improvement of the Quality System.

 Register

Abbott

BioFlorida, Inc. | 901 NW 35th Street | Boca Raton, FL 33431
(P) 561-653-3839 (F) 561-653-3840 admin@bioflorida.com
Membership Management Software Powered by YourMembership  ::  Legal