Dates - 23rd - 24th June 2010, 30th November - 1st December 2010
Price - £1160 + VAT
CAPA is a clearly recognised cGMP regulatory concept that focuses on the systematic investigation of discrepancies(failures and/or deviations) in an attempt to prevent their reoccurrence. To ensure that this is effective, the systematic investigation of the failure incidence is pivotal in identifying the corrective and preventative actions undertaken.
It is a highly interactive course aimed at pharmaceutical professionals who wish to increase their understanding of the mechanics of a systematic investigations process and how the outcomes can be used to ensure effective correction and/or prevention of the reoccurrence of failure.
Course content:
- What are the regulations associated with CAPA
- What do the Regulatory authorities expect
- How do you identify the issue(s) causing failure
- What techniques are available for the analysis of the potential root cause(s)
- How do you define the improvements
- How do you design and implement the solutions
- How do you monitor and verify successful correction/prevention
- How do you ensure effective management notification of CAPA's
To book a training course, please download the booking form
, complete and email to bookings@rssl.com