A Standard Procedure For Quality Assurance Deviation ManagementA deviation is a deviation from the standard procedure or specification which results in non-conforming materials or processes, or in cases…Feb 1, 2022Feb 1, 2022
ISO 11137 meeting the for sterile productsThe ISO 11137 and the sterilization validation is getting more and more in focus during the last years. The notified bodies and the…Jan 13, 2022Jan 13, 2022
To be a CAPA or not be a CAPA that is the question.The CAPA system is the heart of the Quality Management System (QMS) and indicates how effective and compliant your Quality Management…Jan 12, 2022Jan 12, 2022
The new perspective of supplier control after CoronaThe current Corona (Covid-19) pandemic forced the digital transformation of our work environment much quicker than we anticipated. We had…Jan 3, 2022Jan 3, 2022
To be a CAPA or not be a CAPA that is the questionThe CAPA system is the heart of the Quality Management System (QMS) and indicates how effective and compliant your Quality Management…Jan 1, 2022Jan 1, 2022
