By Charity Ogunsanya
Published in: Compliance Online
Published on: November 4, 2023
Description: 90 minute paid webinar
This training program will highlight mistakes often made when corrective and preventative actions are not clearly identified and applied during a manufactured product sterility test failure investigation because an ineffective investigational procedure and tool was used to conduct a sterility test failure investigation. The webinar will also illustrate how avoiding such common mistakes will ensure that these types of products meet the sterility requirements USP and other regulatory guidelines applicable to finished products, bulk drug substance, raw materials or excipients.
Audits • Best Practices • Compliance • Investigations • Laboratory Issues • Methods • Quality • Testing
