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SEARCH RESULTS : 7
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Online Conference Nursing : Recent Updates of FDA 21 CFR 11 Add-On Inspections
Overview: This presentation will cover the scope, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11. This will enable you to determine whether...
Concerned sectors: Public Health -Nursing -
Online Conference Nursing : FDA Process Analytical Method Validation
Overview: An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Why should you Attend: Observati...
Concerned sectors: Medical Equipment -Nursing -
Online Conference Nursing : Dietary Supplements CGMPS - 21 CFR 111 Compliance 2018
Overview: This is to ensure the quality of the dietary supplement and to ensure that the dietary supplement is packaged and labeled as specified in the master manufacturing record. Why should you ...
Concerned sectors: Medical Equipment -Nursing -
Online Conference Nursing : GMP for Phase I Investigational Drug Products 2018
Overview: Phase I clinical trials are the first time that investigational new drugs are introduced into human subjects and, although it is very, very important for all drugs to be manufactured using ...
Concerned sectors: Medical Equipment -Nursing -
Online Conference Public Health : Validation for the New FDA Inspections
Overview: How to conduct a software validation program that will satisfy FDA requirements and produce a safe product. Why should you Attend: There are additional requirements,analyses and tests t...
Concerned sectors: Public Health -
Online Conference Medical Informatics : Compliance for Electronic Records and Signatures 2018
Overview: This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to greatly increase productivity. Areas Covered in the Session: Which data a...
Concerned sectors: Medical Informatics -
Online Conference Medical Informatics : ISO 62366 - How to Conduct a Human Factors
Overview: This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/usability validation. Why should you Attend: We will explain how to...
Concerned sectors: Medical Informatics -
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