This seminar offered in-depth learning on ways by which a firm can define a sustainable structure for its validation program; how Change Control and other quality programs impact the validation program, requirements that go into process design, design of facilities and the qualification of equipment and utilities, and on several other important related areas.

Datacor, Inc., the leading developer and provider of Enterprise Resource Planning (ERP) and Customer Relationship Management (CRM) software solutions for Chemical and Process Manufacturers, announced today the release of its U.S. Food and Drug Administration (FDA) Validation Toolkit for Chempax C/S.

Internationally Recognized Subject Matter Experts to Lead Presentations
Professionals within the engineering, aerospace, quality, medical device and financial industries are invited to attend several webinars.

Klocwork Broadens Security Vulnerability Analysis to Align with Industry and Government Best Practices. Integrated support for CWE, CERT and SAMATE initiatives helps developers eliminate exploitable security issues

Main topic of today is using Agile in an FDA regulated medical device context. Sounds like an impossibility I know, but the folks from Agiletek and Abbott presented a very interesting case study on how they did it.

An abstract syntax tree, or AST for short, is simply a tree-structured representation of the source code as might be typically generated by the preliminary parsing stages of a compiler.