This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review...
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This webinar will teach attendees best practices for conducting effective quality audits to ensure regulatory compliance. Learn how to avoid potential pitfalls during the audit process. Why Should You Attend: Auditing is a critical function within a pharmaceutical or medical device company. Properly performed audits help to ensure that audited parties are operating in accordance with regulatory requirements, procedures, supply/quality agreements, etc. Ultimately audits are a key contributor i...
This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review...
Pharmaceutical packaging and labeling play a pivotal role in the success of any product launch. These activities serve as the essential link between...
This training will review the best practices establishing and conducting a cleaning validation for reusable medical devices. It will also address the...
This webinar will include a detailed discussion of Contract Manufacturing Organizations (CMO) Quality Agreement topics such as change control,...
In this webinar, learn how to implement the changes required by the new regulation EU MDR 745/2017 in your current quality management system in a...
By Olga Golovina On January 1, Ukraine became a full member of the International Criminal Court (ICC), a landmark moment in its efforts to see...
Beginning May of 2025, manufacturers will face more stringent requirements for analytical and clinical validation of laboratory-developed tests...
OTTAWA — A leading gun-control group is accusing the Liberal government of watering down a promise to ensure firearms are properly scrutinized...