Webinar Series on Deviation Management & CAPA: CAPA Effectiveness & System Performance Check

Things will go wrong from time to time. In the world of pharmaceuticals, we need to ensure that we have robust processes and procedures in place to deal with such situations. When an unplanned event arises it must be handled accordingly.

In any case a sound failure investigation is the key to identify appropriate CAPAs. Here it is also important to know how to deal with human error based and non-human error based non-conformances.

Independent from that, it needs to be pointed out that CAPA is an excellent Quality Management tool to continuously improve processes and avoid future failures.

ECA has now set up a series of four Webinars to discuss principles and relevant aspects to implement, improve and monitor your Deviation Management and CAPA System.