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ComplianceOnline Webinar - CE Marking: Obtaining and Maintaining EU Compliance Under the Medical Device Directive(February 11, Friday 10:00 AM PST | 01:00 PM EST) |
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Medical Device Complaints Handling Strategies for Managing Your Biggest Compliance Challenge - Medical Device Webinar By ComplianceOnline (January 27, Thursday 10:00 AM PST | 01:00 PM EST) |
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ComplianceOnline Webinar - Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations(February 03, Thursday 10:00 AM PST | 1:00 PM EST) |
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ComplianceOnline Webinar - Design Validation Protocol and Acceptance Criteria for Chromatographic Methods to meet ICH requirements(January 28, Friday 1:00 PM EST | 4:30 PM EST) |
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Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities - Pharmaceutical Webinar By ComplianceOnline (January 12, Wednesday 10:00 AM PST | 01:00 PM EST) |
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Full day Virtual Seminar - Compliance for 21 CFR Part 11, reducing costs using risk-based computer system validation (January 26, Wednesday 10:00 AM EST | 05:00 PM EST) |
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Regulatory Affairs for Biologics |
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CTD Dossier Requirements: Focus on EU Module 1 and Quality Module 3 |
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Clinical Statistics for Nonstatisticians |
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1st Information Day on the Development Safety Update Report (DSUR) Guidelines ICH E2F |
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