Life sciences companies that develop and bring to market pharmaceuticals, biotechnology, and medical devices face unique needs due to the nature of your business.
• What are your responsibilities?
• How can you expect your software management solutions to assist in the
       validation documentation process?
• When should you bring in a third party validation expert?

Join us as we look into FDA requirements for risk based validation during a live, interactive discussion where we’ll:
• Explore governance structures used to manage compliance;
• Define the role that software management solutions play in regard to systems
       validation and compliance to meet FDA requirements for traceability, tracking,
       and electronic signatures;
• Gain insight on who should play what role while going through the validation
       process.

Following the discussion a live Q&A session will take place – get answers to your critical questions in real-time.

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