This webinar provides step by step instructions on how to design and manage a CAPA system that meets and exceeds compliance requirements.
Details
Discount : Get 15 % Discount as a early bird registrations. Use Promocode CGO15
Why should you attend - CAPA is the most audited Quality subsystem by the FDA.57% of all warning letters send to organizations by the FDA in 2010 were CAPA RELATED.The trend seems to be continuing this year.
Areas Covered in the Session (Bullet points about the proceedings )
CAPA defined
The capa life cycle
CAPA requirements
CAPA design
CAPA documentation
Who will benefit: (Titles)
Quality managers
Quality Engineers
Process Engineers
Manufacturing Engineers
Details
Discount : Get 15 % Discount as a early bird registrations. Use Promocode CGO15
Why should you attend - CAPA is the most audited Quality subsystem by the FDA.57% of all warning letters send to organizations by the FDA in 2010 were CAPA RELATED.The trend seems to be continuing this year.
Areas Covered in the Session (Bullet points about the proceedings )
CAPA defined
The capa life cycle
CAPA requirements
CAPA design
CAPA documentation
Who will benefit: (Titles)
Quality managers
Quality Engineers
Process Engineers
Manufacturing Engineers
