Bulletproofing your cGXP Documentation from Audit Citations

Date: 28-Mar-13 to 28-Mar-13
Location: online compliance panel / San Francisco / California / United States
Category: Healthcare & Pharmaceuticals Conferences & Trade Fairs

Regulators consider documentation to be a critical entity. Consequently, they always audit documentation systems and it is rare to find audits where 483s for poor documentation have not been issued.
By attending this webinar, you will become familiar with what attributes contribute to good document development, 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.

Visitors

The ability to write clear and concise documents is an essential skill required of those working in the Life Sciences industry. This course is ideal for all people who are required to create, complete and/or review documents in the Life Sciences industry.

Exhibitors

The ability to write clear and concise documents is an essential skill required of those working in the Life Sciences industry. This course is ideal for all people who are required to create, complete and/or review documents in the Life Sciences industry.

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