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RESULTAT DE LA RECHERCHE : 23
: 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 -
Cycle de Formation Informatique médical : Preparation of FDA Submissions and Communicating with the FDA | Seminar 2018
Course "Preparation of FDA Submissions and Communicating with the FDA (INDs, NDAs, BLAs, ANDAs, PMAs, 510(k)s, IDEs, Post-Approval Supplements)" has been pre-approved by RAPS as eligible for...
Secteurs concernés: Informatique médical -
Cycle de Formation Informatique médical : New EU Medical Device Regulation | Updated Regulation 2018
Course "The New EU Medical Device regulation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview...
Secteurs concernés: Informatique médical -
Conférences en ligne Management médico-hospitalier : Emergency Communications for Medical Facilities and First Responders
Overview: Webinar participants will be presented with short history amateur radio's development, it's contribution to World War II, advancement of the technology, contribution to the scienc...
Conférences en ligne Biomedical : 3 hour Virtual seminar on FDA's New Enforcement of 21 CFR Part 11
Overview: FDA continues to enforce Part 11 through its ongoing Part 11 inspection and enforcement program. Just in the last 3 years FDA issued more than 30 warning letters with Part 11 relat...
Secteurs concernés: Biomedical -Management médico-hospitalier -
Congrès Chirurgie plastique : IMCAS Asia 2018
For the 12th edition of IMCAS Asia, IMCAS has united with THAICOSDERM & ITCAM in the bustling city of Bangkok, Thailand. From the 13th-15 2018, join plastic surgeons, dermatologists and other aest...
Secteurs concernés: Chirurgie plastique -
Conférences en ligne Management médico-hospitalier : Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Overview: This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Japan....
Conférences en ligne Biomedical : Non-Conforming Material and Failure Investigation
Overview: Non-conforming material happens. And medical device companies must deal it. This 90-minute webinar will help you to make sense of confusing regulations and effectively deal with non-confo...
Secteurs concernés: Biomedical -Management médico-hospitalier -
Conférences en ligne Médecine générale : Process Validation Requirements & Compliance Strategies
Overview: This Process Validation Requirements webinar will review process validation basics, with emphasis on looking beyond compliance towards achieving a robust process. Review of process...
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 -
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