Vertaling van "evaluation of safety " (Nederlands → Frans) :

Evaluation of safety devices for preventing percutaneous injuries among health-care workers during phlebotomy procedures — Minneapolis- St. Paul, New York City, and San Francisco, 1993-1995 MMWR 1997; 46:21-8.
Evaluation of safety devices for preventing percutaneous injuries among health-care workers during phlebotomy procedures — Minneapolis- St. Paul, New York City, and San Francisco, 1993-1995 MMWR 1997 ; 46:21-8.

The evaluation of oncological adverse effects (as well as the evaluation of the Periodic Safety Update Report – PSUR, Annual Safety Report - ASR, Suspected Unexpected Serious Adverse Reaction
The evaluation of oncological adverse effects (as well as the evaluation of the Periodic Safety Update Report – PSUR, Annual Safety Report - ASR, Suspected Unexpected Serious Adverse Reaction

Beschrijving Post-Authorisation Safety Study of Esbriet (Pirfenidone): A Prospective Observational Registry to Evaluate Long-Term Safety in a Real-World Setting.
Description Etude de sécurité après octroi de l’autorisation avec Esbriet (Pirfénidone) : Registre prospectif observationnel afin d’évaluer la sécurité à long terme en contexte de vie réel.

‐ The Mirasol Clinical Evaluation Study Group. A randomized controlled clinical trial evaluating the performance and safety of platelets treated with MIRASOL pathogen reduction technology.
the performance and safety of platelets treated with MIRASOL pathogen reduction technology.

The “PRE pillar” is also responsible for the evaluation of the quality, safety and efficacy of the end products.
The “PRE pillar” is also responsible for the evaluation of the quality, safety and efficacy of the end products.

The evaluation is based on current standards and guidelines on the quality, safety and clinical efficacy of medicines and health products.
The evaluation is based on current standards and guidelines on the quality, safety and clinical efficacy of medicines and health products.

serious adverse events associated with the collection, testing, processing, storage and distribution of blood or blood components that may have an effect on their quality or safety ●● Collecting and evaluating information about
serious adverse events associated with the collection, testing, processing, storage and distribution of blood or blood components that may have an effect on their quality or safety ●● Collecting and evaluating information about

Include mental health in programmes dealing with occupational health and safety. iv. Assess the potential impact of any new policy on the mental well-being of the population before its introduction and evaluate its results afterwards.
Include mental health in programmes dealing with occupational health and safety.

ADI Voor stoffen waarvoor de aanvaardbare dagelijkse opnames (ADI) is vastgesteld op Europees vlak werd rekening gehouden met de gegevens die afkomstig zijn van de EFSA (European Food Safety Authority), de EMEA (The European Agency for the Evaluation of Medical Products) of de SCAN (Scientific Committee on Animal Nutrition).
DJA Pour les substances dont la dose journalière admissible (DJA) a été établie au niveau européen, les données provenant de l’EFSA (European Food Safety Authority), de l’EMEA (The European Agency for the Evaluation of Medical Products) ou du SCAN (Scientific Committee on Animal Nutrition) ont été prises en compte.

The FDA discussions focus on product labeling and Risk Evaluation Mitigation Strategy (REMS) as well as a safety update, but no request for more clinical studies.
Les discussions de la FDA portent sur la notice du produit et sur la stratégie de la gestion des risques (Risk Evaluation Mitigation Strategy ou REMS) ainsi que sur la mise à jour des données sur son innocuité, mais ne requiert pas plus d’études cliniques.