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Fast Facts
Fda Conferences
Results for Conferences on the Category : Fda
When Event Where
May-22-2012Supplier Controls to Meet Tougher U.S. FDA RequirementsUnited States
May-23-2012Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance - Webinar By ComplianceOnlineUnited States
May-24-2012Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanelUnited Kingdom
May-24-2012Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanelUnited States
May-24-2012An Overview of Risk Management and Risk Analysis Techniques in Clinical TrialsUnited States
May-24-2012Statistics for the Non-Statistician - US Seminar 2012 at Washington DCUnited States
May-29-2012Risk-Based Monitoring of Clinical Trials: Say Goodbye to 100% Source Document Verify - Webinar By GlobalCompliancePanelUnited States
May-31-2012How do I Keep FDA Happy with my Contract Manufacturer - Webinar By ComplianceOnlineUnited States
Jun-01-2012Device Corrections and Removals - Webinar By ComplianceOnlineUnited States
Jun-05-2012Excel Spreadsheet Validation to Eliminate 483s - GlobalCompliancePanelUnited States
Jun-06-2012Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanelUnited States
Jun-07-2012FDA Compliant Practice for Labeling and Off-Label Communication Through Social Media - Webinar By GlobalCompliancePanelUnited States
Jun-07-2012FDA Acceptance of non-US Clinical Trials - Webinar By ComplianceOnlineUnited States
Jun-13-2012Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations - Webinar By ComplianceOnlineUnited States
Jun-14-2012Excel Spreadsheet Validation for FDA 21 CFR Part 11 - Webinar GlobalCompliancePanelUnited States
Jun-14-2012REMS Update: Risk Evaluation and Mitigation Strategies - Webinar By ComplianceOnlineUnited States
Jun-18-2012RAPS Approved Seminar on Complying with GMP and CGMP Requirements: Streamlining Quality Assurance and FDA Compliance at MumbaiIndia
Jun-19-2012Webinar by GlobalCompliancePanel Avoiding FDA 483 Observations by Identifying the Root Cause of DeviationsUnited States
Jun-20-2012Medical Device Supplier Quality Agreements - Webinar By GlobalCompliancePanelUnited Kingdom
Jun-21-2012The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations - Webinar By GlobalCompliancePanelUnited States
Jun-21-2012IT Infrastructure and Network Qualification: Step-by-Step - Webinar By GlobalCompliancePanelUnited Kingdom
Jun-21-2012IT Infrastructure and Network Qualification: Step-by-Step - Webinar By GlobalCompliancePanelUnited States
Jun-26-2012Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanelUnited States
Jun-27-2012Trial Master File for Research Sites: Can You Pass FDA Inspection? - Webinar By ComplianceOnlineUnited States
Jun-27-2012FDA Inspections - Do's & Don'ts - Webinar By GlobalCompliancePanelUnited States
Jun-28-2012One and Half-day In-person Seminar: Obtaining and Marketing Your 510(k) with Today's FDA, a 510(k) WorkshopUnited States
Jun-28-2012How to submit a 510(k) and get it cleared from FDA - Webinar By GlobalCompliancePanelUnited States
Jul-12-2012Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial - Webinar By ComplianceOnlineUnited States
Jul-12-2012Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanelUnited States
Aug-08-2012Spreadsheet Validation: Understanding and satisfying FDA requirementsUnited States
Aug-16-2012CAPA Systems for Medical Device Manufacturers - Seminar By ComplianceOnlineUnited States
 
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