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March 30, 2022 from 10am to 1pm – online This project management training for FDA regulated companies will show how you can meet key FDA and EU MDD regulatory requirements for the project you manage. It will focus on proven tools and techni… Organized by Complianceonline | Type: webinar
March 29, 2022 from 10am to 1pm – online This webinar will go through every section of the revised FFIEC Bank Secrecy Act/Anti-Money Laundering Examination Manual to highlight changes and areas where banks should review their internal polic… Organized by ComplianceOnline | Type: webinar
March 28, 2022 from 10am to 1pm – online An ANDA is an Abbreviated New Drug Application. This application is submitted to the FDA to seek approval to produce a U.S. generic drug from an existing patented approved drug. The ANDA is submitted… Organized by Complianceonline | Type: webinar
March 24, 2022 from 10am to 1pm – online The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. Thi… Organized by Complianceonline | Type: webinar
March 23, 2022 from 10am to 1pm – online Hygienic Design in food processing is a given, however FDA’s #483 violations continue to reflect organizations clearly lack the necessary requirements to maintain safe environments for food productio… Organized by ComplianceOnline | Type: webinar
March 23, 2022 from 10am to 1pm – online This webinar will focus on regulatory requirements, optimal processes and define the difference in collaboration with both internal and external physician advisor roles. It will also discuss the role… Organized by ComplianceOnline | Type: webinar
March 23, 2022 from 10am to 1pm – online This 21 CFR Part 11 compliance training will guide you through the requirements of Part 11 and will also explain its 3 primary areas: SOPs, product features and validation (10 step risk based approac… Organized by ComplianceOnline | Type: webinar
March 21, 2022 from 7am to 10pm – online This course will give an introduction into the Medical Device Single Audit Program (MDSAP) and how to adjust your internal audit program. The introduction will give an overview about the requirements… Organized by ComplianceOnline | Type: webinar
March 18, 2022 from 10am to 1pm – online Batch record review is an important step in the release of a medicinal product. This webinar sets out the regulatory requirements for batch records and sets out a systematic approach for review. Tren… Organized by ComplianceOnline | Type: webinar
March 17, 2022 from 10am to 1pm – online This webinar will discuss what are Mycotoxins, classifications, contamination methods, the Regulations & Recommendations on Maximum Mycotoxin Levels, the risk management and prevention strategies… Organized by Complianceonline | Type: webinar
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