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  1. Method Development and Validation for Assays Supporting Testing of Biologics
    Deadline: 2021-06-14 Event Date: 2021-06-24 - 2021-06-25
    Venue: Virtual Seminar, USA - United States
  2. Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
    Deadline: 2021-05-16 Event Date: 2021-05-26
    Venue: Virtual Seminar, USA - United States
  3. Internal Audit, Fraud Risk Assessment and Risk Management Annual Plan
    Deadline: 2021-05-15 Event Date: 2021-05-25 - 2021-05-26
    Venue: Virtual Seminar, USA - United States
  4. FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
    Deadline: 2021-05-10 Event Date: 2021-05-20 - 2021-05-21
    Venue: Virtual Seminar, USA - United States
  5. Change Control Best Practices - Avoiding Unintended Consequences of Changes
    Deadline: 2021-05-08 Event Date: 2021-05-18 - 2021-05-19
    Venue: Virtual Seminar, USA - United States
  6. Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
    Deadline: 2021-05-07 Event Date: 2021-05-17 - 2021-05-18
    Venue: Virtual Seminar, USA - United States
  7. REACH and RoHS Compliance: Gain a Deeper Understanding
    Deadline: 2021-05-07 Event Date: 2021-05-17 - 2021-05-18
    Venue: Virtual Seminar, USA - United States
  8. Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies
    Deadline: 2021-04-23 Event Date: 2021-05-03 - 2021-05-04
    Venue: Virtual Seminar, USA - United States
  9. Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
    Deadline: 2021-04-30 Event Date: 2021-05-10 - 2021-05-11
    Venue: Virtual Seminar, USA - United States
  10. How to Prepare an Effective Audit Manual for an Internal Audit Department
    Deadline: 2021-05-09 Event Date: 2021-05-19
    Venue: , USA - United States