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RESULTAT DE LA RECHERCHE : 40
: device:
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Colloque Informatique médical : Medical Device Software: An Incremental Approach to Risk and Quality Management
Course "Medical Device Software: An Incremental Approach to Risk and Quality Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recert...
Secteurs concernés: Informatique médical -
Conférence / Séminaire Acupuncture : Strategies for Improving Effectiveness and Efficiency of your Quality Management System Seminar
Course "Strategies for Improving Effectiveness and Efficiency of your Quality Management System" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RA...
Conférence / Séminaire Acupuncture : Examination of Laboratory, Medical and Device issues including Performance, Risk and Validation following Regulatory and ICH Statistical Guidelines Seminar
Course "Examination of Laboratory, Medical and Device issues including Performance, Risk and Validation following Regulatory and ICH Statistical Guidelines" has been pre-approved by RAPS as ...
Secteurs concernés: Acupuncture -Droit et santé -
Conférence / Séminaire Informatique médical : Data Integrity: Learn to Comply with the FDA Expectations and Avoid Facing Penalties ranging from Public Warning Letters to Criminal Charges and Product Removal from the Market Place
Course "Data Integrity: Learn to Comply with the FDA Expectations and Avoid Facing Penalties ranging from Public Warning Letters to Criminal Charges and Product Removal from the Market Place"...
Secteurs concernés: Informatique médical -
Conférence / Séminaire Droit et santé : HIPAA Compliance 2018 Seminar
Overview: This two-day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being, and its evolution...
Secteurs concernés: Droit et santé -
Conférences en ligne Biotechnologie : Revolutionary Change in FDA Software Regulation
Overview: It is not about giving an OK to products, it is about trusting the manufacturer to do the right thing. Overall, your regulatory approach to software regulation needs to ease up and reap the...
Secteurs concernés: Biotechnologie -
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 : 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
  Course "21 CFR Part 11 Compliance for Computer Systems Regulated by FDA" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertif...
Secteurs concernés: Biomedical -Management médico-hospitalier -
Conférence / Séminaire Management médico-hospitalier : Understanding the HIPAA/HITECH Requirements | Washington Seminar
Description: This one-day seminar will get into the fine details of what we need to do and how to do it. We will go point by point through the entire HIPAA Security Rule and uncover simple methods...
Conférences en ligne Biotechnologie : Compliance for Electronic Records and Signatures (21 CFR Part 11)
Overview: Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based valida...
Secteurs concernés: Biotechnologie -
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