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RESULTAT DE LA RECHERCHE : 15
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Conférences en ligne Biomedical : 3-Hour Virtual Seminar on DHF, DMR, DHR, TF , Design Dossiers - The Requirements
Overview: This webinar will examine the existing and proposed requiements for the U.S. FDA's DHF, 21 CFR 820.30 and now ISO 13485:2016 7.3 including its derivitive documents, the DMR and...
Secteurs concernés: Biomedical -Management médico-hospitalier -
Conférence / Séminaire Acupuncture : Governance and Change Control According to GxP/GMP Requirements
Course "Governance and Change Control According to GxP/GMP Requirements " has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon ...
Conférence / Séminaire Acupuncture : Clinical Evaluation Report for Europe and MEDDEV Expectations: Impact with New Medical Device Regulations (MDR) Seminar
Course "Clinical Evaluation Report for Europe and MEDDEV Expectations: Impact with New Medical Device Regulations (MDR)" has been pre-approved by RAPS as eligible for up to 12 credits toward...
Secteurs concernés: Acupuncture -Droit et santé -
Conférence / Séminaire Acupuncture : European Medical Device Regulation / key changes overview
Course "European Medical Device Regulation / key changes overview" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full co...
Secteurs concernés: Acupuncture -Biomedical -
Conférence / Séminaire Management médico-hospitalier : Tougher Import Rules for FDA Imports in 2018
Course "Tougher Import Rules for FDA Imports in 2018" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Des...
Secteurs concernés: Management médico-hospitalier -_Autres -
Conférences en ligne Biomedical : When to Submit a 510(k) for a Change to an Existing Device
Overview: This presentation, will aid manufacturers of medical devices who intend to modify a 510(k)-cleared device or a preamendments device subject to 510(k) Why should you Attend: This present...
Secteurs concernés: Biomedical -Santé publique -
Conférences en ligne Santé publique : Design Control is Critical to Product Quality
Overview: This 90-minute webinar will cover the basics of design controls for medical devices. Design Controls are an integrated set of management practices that are customer focused and ensure quali...
Secteurs concernés: Biotechnologie -Santé publique -
Conférences en ligne Biochimie : Verification vs Validation-Product, Equipment and QMS Software
Overview: You will learn What do the U.S. FDA and EU Expect for Verification and Validation, Actions and documentation to meet U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements...
Secteurs concernés: Biochimie -Biotechnologie -
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 : 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...
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