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RESULTAT DE LA RECHERCHE : 30
: Devices:
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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 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 : 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 -
Conférences en ligne Informatique médical : Improving Compliance and your Company's Bottom Line (MedicalDevice Cybersecurity)
Overview: This session will provide some insight into current trends in cybersecurity threats to medical devices and how to follow industry best practices to prevent and/or mitigate these threats. Cy...
Secteurs concernés: Informatique médical -
Conférences en ligne Biotechnologie : Quality Agreements Made Easy (Advanced 2018)
Overview: The requirements for the assurance of quality within networks and circles of entities whose responsibilities are increasing specialized present an especially vexing challenge to the managem...
Secteurs concernés: Biomedical -Biotechnologie -
Conférences en ligne Biotechnologie : Risk Control According to (GxP-GMP) Requirements
Overview:  GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics. Documentation is a critical tool for...
Secteurs concernés: Biotechnologie -
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