Vertaling van "clinical task " (Nederlands → Frans) :

Regelmatige overlegplatforms met stakeholders zoals: ●● Clinical Task Force ●● Overleg FAGG - APB en OPHACO ●● Overleg FAGG - Industrie ●● Overleg FAGG - Medische hulpmiddelen ●● Overleg FAGG - Ziekenhuisapothekers ●● TOR ●● V-amazone
stakeholders telles que : ●● Clinical Task Force ●● Concertation AFMPS - APB et OPHACO ●● Concertation AFMPS - Industrie ●● Concertation AFMPS - Dispositifs médicaux ●● Concertation AFMPS - Pharmaciens hospitaliers ●● TOR ●● V-amazone

° Canadian Medical Association [Clinical Practice Guidelines] ° Canadian Task Force on Preventive Health Care ° Clinical practice guidelines [Guidelines Advisory Committee Ontario]
° Canadian Medical Association (Clinical Practice Guidelines) ° Canadian Task Force on Preventive Health Care ° Clinical practice guidelines (Guidelines Advisory Committee Ontario)

° American College of Physicians ° Primary Care - Clinical Practice Guidelines ° U.S. Preventive Services Task Force Guide to Clinical Preventive Services ° AHRQ [Agency for Healthcare Research and Quality]
° American College of Physicians ° Primary Care - Clinical Practice Guidelines ° U.S. Preventive Services Task Force Guide to Clinical Preventive Services ° National Guideline Clearinghouse ° AHRQ (Agency for Healthcare Research and Quality) ° Evidence-Based Clinical Practice Guidelines (US) - Pédiatrie

with the existing Ethics Committees via the Clinical Trial Task Force (CTTF), an informal structure established in 2003 under the FAMHP mission.
with the existing Ethics Committees via the Clinical Trial Task Force (CTTF), an informal structure established in 2003 under the FAMHP mission.

De Clinical Trial Task Force (CTTF) is een informeel overlegorgaan waar de verschillende belanghebbenden rond de tafel zitten.
Le Clinical Trial Task Force (CTTF) est un organe informel de concertation où les différents intéressés s’assoient autour de la table.

The European Directive 2001/20, transposed in the law of 7 May 2004, forms the basis for the department’s core tasks: ●● Validating, evaluating and assigning approvals for the conduct of clinical trials (including declarations) ●● Strategic preparation of the associated GCP
The European Directive 2001/20, transposed in the law of 7 May 2004, forms the basis for the department’s core tasks: ●● Validating, evaluating and assigning approvals for the conduct of clinical trials (including declarations) ●● Strategic preparation of the associated GCP

Unit I Unit I is responsible for the tasks of the secretariat of the commission for the establishment of retail pharmacies, of the secretariat of the commission for the recognition of pharmacists-clinical biologists, of the retail pharmacies registry and plays an important role in the problems of products in the “grey area” (these are “borderline” products whose exact status has to be determined: is it a medicine or not?).
Unit I Unit I is responsible for the tasks of the secretariat of the commission for the establishment of retail pharmacies, of the secretariat of the commission for the recognition of pharmacists-clinical biologists, of the retail pharmacies registry and plays an important role in the problems of products in the “grey area” (these are “borderline” products whose exact status has to be determined: is it a medicine or not?).

: voorzitters van de politieke groepen van de Vertegenwoordigers van de Kamer en van de Senaat Clinical Trial Task Force Raadgevend Comité voor Bio-ethiek Vlaams Patiëntenplatform.
Clinical Trial Task Force Comité consultatif de bioéthique. Vlaams Patiëntenplatform