general medical devices compliant with the EU medical devices directive (EU MDD) or EU active implantable medical devices directive (EU AIMDD) with a valid declaration and CE marking can be placed on the Great Britain market up until the sooner of expiry ...
To navigate this process,MedCastserves as a web-based Medical Device Centralized Online Application System for MDA registration. However, utilization of MedCast is restricted to local Authorized Representatives. These Malay representatives need to possess an establishment license along with a ce...
Abubakar Dr Ahmed, NigeriaAcob Joel, Philippines Adeke Dr Azuka, NigeriaAffey Dr. Fatuma, Kenya Agogo George, KenyaAguiyi-ikeanyi Chinelo, Nigeria Ahmed Anas Guerboub, MoroccoAhyayauch Hasna, Morocco Ait Addi Rachid, MoroccoAjam Qais, Iraq ...
Karthick Subramanian Jawaharlal Institute of Postgraduate Medical Education and Research, India Vesna Ambarkova Saints Cyril and Methodius University of Skopje, Macedonia Ana Beatriz Gorini da Veiga Federal University of Health Sciences of Porto Alegre, Brazil Duncan B Johnstone Temple University School of...
In addition, the Philippines may also require documents such as a quality systems certificate of approval and a certificate of agreement between a distributor and the manufacturer. The list of devices that must be registered was most recently released in February 2014; the Philippines wi...