WHO global model regulatory framework for medical devices including in vitro diagnostic medical devices
World Health Organization. (2017). WHO global model regulatory framework for medical devices including in vitro diagnostic medical devices. World Health Organization. https://apps.who.int/iris/handle/10665/255177. License: CC BY-NC-SA 3.0 IGO
WHO Medical device technical series
MetadataShow full item record
Showing items related by title and subject
Adherence of preventive oral care products in the Syrian market to evidence-based international recommendations Habes, D.; Mahzia, R.; Nakhleh, K.; Joury, E. (World Health Organization, Regional Office for the Eastern Mediterranean, 2016-06)No study has investigated the availability and adherence of preventive oral care products on the Syrian market to evidence-based international recommendations. Data were collected in 2012, and updated in 2016, in terms of ...
The selection and use of essential in vitro diagnostics: report of the second meeting of the WHO Strategic Advisory Group of Experts on In Vitro Diagnostics (including the second WHO model list of essential in vitro diagnostics) World Health Organization (World Health Organization, 2019)
Biologicols Unit and Expanded Programme on Immunization : WHO European Region Workshop on testing of DPT vaccine with emphase on in vitro methods = Service des produits biologiques et Programme élargi de vacciaation : Atelier de la Région européenne de TOMS sur les méthodes d'épreuve du vaccin DTC, notamment sur les méthodes in vitro World Health Organization (1991)