Print Page | Contact Us | Sign In | Join
Pharmaceutical Current Good Manufacturing Practices in the United States and Europe | Alachua
Tell a Friend About This EventTell a Friend
 

6/8/2015
When: 06/08/2015
10:00 AM - 12:00 PM
Where: Biotility UF CERHB
13706 Innovation Drive
Alachua, Florida  32615
United States
Contact: Tammy Mandell
(386) 462-6397

« Go to Upcoming Event List  

Pharmaceutical Current Good Manufacturing Practices in the United States and Europe: Similarities and Differences

Pharmaceutical cGMPs are in effect in 104 countries, either through national codes, adherence to regional codes, or adoption of the WHO code. The United States Food and Drug Administration (FDA) and Europe's European Medicines Agency (EMA) are two of the major global bodies that oversee pharmaceutical cGMPs. Participants in this course will learn similarities and differences between the FDA and EMA cGMP terminology and regulations, including cleanroom standards, environmental monitoring practices, the roles of the Quality Assurance Director (FDA) and Qualified Person (EMA), internal audits, and contract manufacturing.

DATE: June 8, 2015 TIME: 10:00-12:00 PRICE: $75

REGISTER

About BioFlorida

BioFlorida represents nearly 6,000 establishments and research organizations in the biopharmaceutical, medical technology and bioagriculture sectors that collectively employ nearly 83,000 Floridians.

 

Members of the BioFlorida network include emerging and established life science companies, universities, research institutions, hospitals, medical centers, incubators, economic development agencies, investors and service providers.

 

Email us for a regional Chapter sponsorship.

Connect