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How to Bullet Proof your Documents from Most Commonly Cited GDP Violations

10/22/2013 10:00 AM - 11:00 AM

How to Bullet Proof your Documents from Most Commonly Cited GDP Violations

Good documentation is a cornerstone for good operational practices in any biopharmaceutical company. While documentation is a CFR requirement, there is no specific regulatory guidance on good documentation practices. A company’s documentation system and practices are vital to a successful audit since it provides regulators a window into the company’s operations. It is one of the systems which always attract the attention of regulators.

Documentation system is one of the systems that are always audited. It is rare to find an audit which does not issue a 483 for poor documentation. Add to this a level of complexity introduced by documentation in the electronic realm and soon we increase our vulnerability to receiving 483s for documentation.

The webinar, ‘Building How to Bullet Proof your Documents from Most Commonly Cited GDP Violations’ being conducted on 22-Oct-2013, will provide comprehensive understanding of the Good Documentation Practices (GDPs) requirements, and help know the complexities and challenges posed by hybrid documentation systems and steps you absolutely need to take to ensure that your documentation system is bullet proof.

For more information about the webinar, please visit

http://www.complianzworld.com

Learn More: How to Bullet Proof your Documents from Most Commonly Cited GDP Violations

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