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Validation: : Prochains Evénements, congres, formations, conférences medicales

SPECIALITES MEDICALES
RECHERCHER UN EVENEMENT, CONGRES, FORMATION MEDICALE
CONGRES, FORMATIONS, EVENEMENTS A VENIR
RESULTAT DE LA RECHERCHE : 12
: Validation:
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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 : FDA Software Monsters Cybersecurity, Interoperability, Mobile Apps and Home Use
Race "FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC r...
Secteurs concernés: Acupuncture -Droit et santé -
Conférence / Séminaire Acupuncture : A Risk Based Approach to Excel Compliance with the FDA's 21 CFR 11 and the European Annex 11
Course "A Risk Based Approach to Excel Compliance with the FDA's 21 CFR 11 and the European Annex 11" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant...
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 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 -
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 Biotechnologie : Highlights of FDA GLP Regulations and the (Roles) and Responsibilities
Overview:  This 3 hour GLP virtual seminar will discuss various GLP regulations (FDA/OECD GLP's) along with highlighting roles and responsibilities of management and key personnel involved i...
Secteurs concernés: Biomedical -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 -
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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