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RESULTAT DE LA RECHERCHE : 5
: Inspections:
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Conférence / Séminaire Biotechnologie : What you Need to Know to Prepare FDA Inspection
Overview: Although an effective Quality System should always be inspection ready, many medical device companies make basic mistakes during inspections leading to 483s and even warning letters. This w...
Secteurs concernés: Biotechnologie -
Conférence / Séminaire Management médico-hospitalier : How to be efficient and compliant with 21 CFR Part 11, data integrity, and SaaSCloud
Course "How to be efficient and compliant with 21 CFR Part 11, data integrity, and SaaS/Cloud" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RA...
Secteurs concernés: Biomedical -Management médico-hospitalier -
Conférence / Séminaire Management médico-hospitalier : Seminar on Hosting FDA Regulatory Inspections in San Diego
Course "Hosting FDA Regulatory Inspections" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Descriptio...
Secteurs concernés: Biomedical -Management médico-hospitalier -
Conférences en ligne Biotechnologie : FDA continues to enforce through its new 21 CFR Part 11 inspection
Overview: The webinar will have the answers. In addition, using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare thei...
Secteurs concernés: Biotechnologie -
Conférence / Séminaire Management médico-hospitalier : How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection
Course "How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection" has been pre-approved by ...
Secteurs concernés: Biomedical -Management médico-hospitalier -
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