Take part in our webinar on Tuesday 10 December at 3PM London / 10AM New York to learn how a tactical and well planned-out remediation effort is key to lasting maintainable corrections.
Furthermore, you can gain insight on how NSF uniquely views the process, executing using our industry experience to ensure that when new systems are put in place, they will address overlooked aspects of remediation, the underlying causes and the support systems that drive actual sustainable change and provide fundamental success factors.
Jesse Ahrendt will be presenting the webinar. Ahrendt is an experienced industry consultant with over 20 years of active engagement in pharmaceuticals, medical devices and biotechnology as a certified Quality Auditor and Quality Engineer.
His areas of expertise include QA Compliance, third-party vendor evaluation, cGMP manufacturing, quality systems and quality auditing including CAPA, Investigations, validation, mock inspection, supplier qualification, QMS, risk assessment and procedural updates.
NSF provides a comprehensive range of pharmaceutical support services, including consulting, auditing, training and regulatory compliance, helping clients to address industry challenges and public health and safety concerns, as well as meet the stringent requirements of the pharmaceutical industry.
For more information on how to sign up to the webinar, please fill out the enquiry form attached to this page.