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

SPECIALITES MEDICALES
RECHERCHER UN EVENEMENT, CONGRES, FORMATION MEDICALE
CONGRES, FORMATIONS, EVENEMENTS A VENIR
RESULTAT DE LA RECHERCHE : 16
: regulations:
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Cycle de Formation Informatique médical : A Risk Based Approach to IT Infrastructure & Cloud Qualification, Compliance & Control
Course "A Risk Based Approach To IT Infrastructure & Cloud Qualification, Compliance & Control" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant&#...
Secteurs concernés: Informatique médical -
Colloque Informatique médical : 21 CFR Part 11 compliance for software validation and SaaS/Cloud Seminar 2018
Course "21 CFR Part 11 compliance for software validation and SaaS/Cloud" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon ...
Secteurs concernés: Biologie -Biotechnologie -Médecine du travail -
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 : Writing & Managing Effective SOPs Seminar 2018
Course "Writing & Managing Effective SOPs" 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 -
Cycle de Formation Informatique médical : How to Register and Maintain Various Types of Combination Products | Seminar 2018
Course "Combination Products" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This seminar pr...
Secteurs concernés: Informatique médical -
Conférences en ligne Médecine générale : How to Correctly Submit Pharmacogenomics Data for Faster Approval by the Agency, and What to Expect from the Regulatory Agencies in the Near Future
Overview: This presentation, will describe the agency expectations, describe how to correctly submit pharmacogenomics data for faster approval by the agency, and what to expect from the regu...
Conférences en ligne Biomedical : Auditing Analytical Laboratories for FDA Compliance
Overview: Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requi...
Secteurs concernés: Biomedical -Management médico-hospitalier -
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 -
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....
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