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Good Documentation Practices and Quality Assurance
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Establishing and maintaining a robust documentation system is critical to achieving regulatory compliance in the biotechnology industry. Participants in this one-day course will learn how to develop, organize, and store documents as part of a Quality Management System. Additional topics to be covered include documentation types and their specific applications, document features that provide objective evidence for activities performed (or results achieved) & document control.

2/10/2015
When: 02/10/2015
9:00 AM - 4:00 PM
Where: Biotility UF CERHB
13706 Innovation Drive
Alachua, Florida  32615
United States
Contact: Tammy Mandel
(386) 462-6397

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Good Documentation Practices and Quality Assurance

Establishing and maintaining a robust documentation system is critical to achieving regulatory compliance in the biotechnology industry. Participants in this one-day course will learn how to develop, organize, and store documents as part of a Quality Management System. Additional topics to be covered include documentation types and their specific applications, document features that provide objective evidence for activities performed (or results achieved), document control, employee training on documents, document review, approval, and revision, template designs, and practice writing SOPs and creating documents such that they may be accurately utilized for their intended purpose.

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DATES: February 10, 2015
PRICE: $350

TIME: 9:00 a.m. - 4:00 p.m.

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.

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