The new MedTech Europe Code of Ethical Business Practice sets strict, clear and transparent rules for the industry’s relationship with Healthcare Professionals (HCPs) and Healthcare Organizations ... SNITEM SPECTARIS SVDI/ASID Swedish Labtech Swedish MedTech VDGH Information obtained from www.medtecheurope.org. He is a speaker at the MedTech Forum 2018 and his sessions include: CEO #NOFILTER and The MedTech Europe Code as a Business Enabler, both on Thursday 25th of January. The 11 pages template is provided in a form of a Word document template (no … Comms strategy for Q2 2018. SNITEM (member of EUCOMED), SFRL (member of EDMA), LEEM French Board of Doctors’ ... AMID Code on Interactions with HCPs - AMID Código de Interacción jul2009_E AMID Code of Ethics - amid_cod_etica_trad ucido abril11.pdf ... Sweden SWEDISH MEDTECH (member of EUCOMED) SWEDISH LABTECH (member of EDMA) The Code also introduces a common independent enforcement mechanism. Since 01.2015, I am Head of Compliance EMEA-LATAM (+6700 employees, +155 countries) & RDI (Rotkreuz Site, +2600 employees), Member of the EMEA-LATAM Operating Committee and Member of the Roche Group Healthcare Compliance Council. For this reason, this template suggests the contractual clauses to be included in the quality agreement between Distributor/Importer and Manufacturer. In my role, I coordinate a compliance network of +40 Compliance Officers, set compliance targets for the Region and supervise & … Founded in 1959, COCIR is a non-profit association headquartered in Brussels (Belgium) with a China Desk based in Beijing since 2007.COCIR is unique as it brings together the healthcare, IT and telecommunications industries. It will set the minimum standard by which industry members operate across Europe. COCIR is the European Trade Association representing the medical imaging, radiotherapy, health ICT and electromedical industries. The toss of a dice. The new MedTech Europe Code of Ethical Business Practice sets strict, clear and transparent rules for the industry’s relationship with Healthcare Professionals (HCPs) and Healthcare Organizations ... SNITEM SPECTARIS SVDI/ASID Swedish Labtech Swedish MedTech VDGH Information obtained from www.medtecheurope.org. MedTech Europe Code Applicable National Code banning DS in place or agreed (entry into effect of prohibition may be later) DS prohibited by law or stakeholder agreement eSB ... France Snitem To be determined Statement by Board (Nov. 2015) not to transpose the Code SIDIV To be determined Discussions ongoing. Under the MDR, it has become crucial to ensure smooth and transparent cooperation among all the economical operators involved in the Medical Devices supply chain. An incoming tornado. Brussels, 2 December 2015 Members of the European Diagnostics Manufacturers Association (EDMA) and of the European Medical Technology Industry (Eucomed), both members of MedTech Europe, have approved a new Code of Ethical Business Practice at their General Assemblies held on 2 December in Brussels, in a continuous effort to set high ethical standards for the medical technology industry … 4 The existence of two codes created confusion; there was a need to introduce clarity to the rules applicable to the industry An updated, joint MedTech Europe code needed to reflect how society had evolved EDMA/Eucomed codes - drafted in 2007/200 – were dated and included inconsistencies and contradictions www.medtecheurope.org Rationale for the revision of previous Codes of Ethics The decline of investment in medtech. COCIR. Slovenia SLO-MED yes Code fully into force as of 1.1.2018 Slovenia SIEDMA yes Code fully into force as of 1.1.2018 Spain FENIN yes Board approval on 20.12.2016, DS banned as of 1.1.2018 Sweden Swedish Medtech N/A Agreement with stakeholders, no transposition needed. Alignment with MTE Code already the … For more information go to the MTF website and follow #MTF2018 on Twitter. The new MedTech Europe Code of Business Practice will become binding for EDMA and Eucomed corporate members by 1st January 2017. 2019 -14 Explanatory note on MDR Codes 2019-13 Guidance on sampling of MDR Class IIa / Class IIb and IVDR Class B / Class C devices for the assessment of the technical documentation ( MCDG ) 2019-12 Designating authority’s final assessment form : Key Information (EN) ( MDCG )