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ComplianceOnline Webinar - Excel Spreadsheets - Develop and Validate to Eliminate 483s(November 05, Friday 10:00 AM PDT | 01:00 PM EDT) |
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ComplianceOnline Webinar - The Tougher U.S. FDA - One Year Later(October 19, Tuesday 10:00 AM PDT | 01:00 PM EDT) |
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ComplianceOnline Webinar - Developing Supplier Quality Auditor Training Programs(September 21, Tuesday 09:00 AM PDT | 12:00 PM EDT) |
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ComplianceOnline Webinar - Best Practices for Managing FDA Investigators and Handling FDA 483 Observations(September 30, Thursday 10:00 AM PDT | 01:00 PM EDT) |
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ComplianceOnline Webinar - Critical Role of Quality Audit in GxP Compliance & Improvement(September 29, Wednesday 09:00 AM PDT | 12:00 PM EDT) |
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ComplianceOnline Webinar - Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs(October 19, Tuesday 10:00 AM PDT | 01:00 PM EDT) |
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ComplianceOnline Webinar - Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective(October 12, Tuesday 10:00 AM PDT | 01:00 PM EDT) |
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ComplianceOnline Webinar - The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development(October 05, Tuesday 10:00 AM PDT | 01:00 PM EDT) |
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ComplianceOnline Webinar - Ensuring GCP compliance through quality auditing in clinical trial(September 29, Wednesday 10:00 AM PDT | 01:00 PM EDT) |
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ComplianceOnline Webinar - How to Use Foreign Trial Data in Your NDA Approval Process(September 28, Tuesday 10:00 AM PDT | 01:00 PM EDT) |
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