Employers AESGP and Medtech call for a moratorium on the implementation of the new Medical Devices Regulation 2017/745.
AESGP and Medtech call for a moratorium on implementation of the new Medical Devices Regulation
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Masterclass on ‘Aesthetic Equipment and Products’ at Beauty Cluster Barcelona
The Masterclass 'Equipment and Aesthetic Products', organised by Beauty Cluster Barcelona, Beauty Business School and the Gabinete Técnico Farmceútico...
Regulation of aesthetic products and equipment: new session at BCB
Regulation of Aesthetic Equipment and Products: a training session by Mercè Camps and Quim Gómez for Beauty Cluster Barcelona.
Corrigendum to the Medical Devices Regulation 2017/745: erratum by the European Commission
Corrigendum to the Medical Devices Regulation - The European Council presented on 25 November in Brussels a Corrigendum to the Medical Devices Regulation 2017/745. This publication consists of a correction of up to 11 citation errors in the original text of the Regulation.
Conference on the new Medical Devices Regulation in Valencia (update)
Medical Devices in Valencia - On Wednesday 27th November, a conference on the new Medical Devices Regulation was organised at the...
Chronicle of the Training on the new Medical Devices Regulation
Chronicle of the Training on the new Medical Devices Regulation - On April 4th, the GTF Technical Office organised a Training Day on the new...
Chronicle of Infarma 2019: the congress returns to Barcelona
This March, the 31st European Congress and Exhibition of the Pharmacy Office, Infarma 2019, was held in Barcelona. A meeting where, year after year,...
Carmen Ruiz-Villar, new Head of the Medical Devices Department
The Presidency of the Spanish Agency for Medicines and Health Products (AEMPS) published in the Official State Gazette of 30 November an agreement of the...
Health Authorisation for PS advertising: Salut closes the face-to-face route
The Catalan Department of Health has abolished the face-to-face procedure for applications for health authorisation for advertising of PS and IVDs. Since...
Update on the Regulation of Medical Devices: UB-IL3 course
Update on Medical Devices Regulation - In 2017, Regulation 745/2017 on Medical Devices and Regulation...
Courses at GTF: postponed course with INTERCER on ISO 13485 for Internal and External Auditors
GTF courses (update) - Due to scheduling incompatibilities between GTF and Intercer technicians, the Auditor courses are delayed...
mHealth BCN Conference: Apps and Medical Devices
Joaquín Gómez Abril, technical expert in CE Marking of Medical Devices of the Notified Body (NB) Kiwa and in collaboration with GTF M. Camps,...