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  1. Special Considerations during Medical Device Design: Dos and Don'ts
    Deadline: 2014-11-26Event Date: 2014-11-26Venue: Houston, USA - United States of America
  2. 21 CFR Part 11 Add-On Inspections by the FDA
    Deadline: 2014-11-20Event Date: 2014-11-20Venue: Houston, USA - United States of America
  3. Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
    Deadline: 2014-11-19Event Date: 2014-11-19Venue: Houston, USA - United States of America
  4. Internet Issues for FDA-Regulated Industry – A Review of Issues Involving Social Media
    Deadline: 2014-11-18Event Date: 2014-11-18Venue: Houston, USA - United States of America
  5. Bioterrorism and Food Security-A Cultural Conundrum
    Deadline: 2014-11-14Event Date: 2014-11-14Venue: Houston, USA - United States of America
  6. Best Practices for Quality Risk Management for Pharmaceutical Industry
    Deadline: 2014-11-13Event Date: 2014-11-13Venue: Houston, USA - United States of America
  7. Meet the New, Tougher FDA Expectations
    Deadline: 2014-11-12Event Date: 2014-11-12Venue: Houston, USA - United States of America
  8. US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus
    Deadline: 2014-11-10Event Date: 2014-11-10Venue: Houston, USA - United States of America
  9. 21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration
    Deadline: 2014-11-04Event Date: 2014-11-04Venue: Houston, USA - United States of America
  10. Patient Rights and the HIPAA Privacy Officer - Meeting Patient Desires and Avoiding Penalties
    Deadline: 2014-11-04Event Date: 2014-11-04Venue: Houston, USA - United States of America