Services for manufacturers

Posts - that's to be discovered on the topic (10)

IE Life Science July 24, 2022
Showcase

TS Quality & Engineering September 9, 2021
Showcase

Start creating your MDR Transition Plan

The website eu-mdr.eu is intended to help companies from different sectors and with different products to reach the safe haven of MDR conformity in an efficient way.

Swiss Medtech Expo 2021

RMS Foundation January 13, 2021
Showcase

Particle analysis after dynamic loading of medical devices

Many medical devices consist of several components and are exposed to cyclical loads during use. Resulting micromovements can generate abrasion particles. To prove the safety of a product, it is often necessary to determine the type, quantity and size of the wear particles.

EPHJ July 16, 2020
Story

EPHJ is stepping up and announces 2020 edition

Having been obliged to postpone its 2020 edition to September due to Covid-19, the largest annual trade fair in Switzerland will in fact take place this year in Geneva to contribute to the recovery of all the high-precision sectors.

RMS Foundation April 2, 2020
Showcase

Fatigue Resistance of AM-Structures

A special grid structure made of Ti6Al4V was deposited on a bar using additive manufacturing (AM). There were small metallic droplets on the surface. Fatigue tests resulted in early failures because of the higher hardness of the AM-structures and the interface compared to the bulk material.

EXCO Consulting GmbH August 8, 2019
Showcase

Gap analysis for established product technical documentation

To continue offering his products on the market, a customer had to check the documentation of existing product lines and adapt it to current regulations. With the support of EXCO, he was able to close the gaps in the shortest possible time and pass the subsequent TÜV audit.

Swiss Medtech Expo 2019

EXCO Consulting GmbH August 8, 2019
Service

With EXCO for MDR / IVDR Compliance

We offer solutions for the regulated market. EXCO examines your processes and documentation for compliance with the requirements of the new EU MDR / IVDR. This includes individual consultation with recommendations for action and the specific implementation of entire work packages.

Swiss Medtech Expo 2019

epmodex AG July 30, 2019
Showcase

Updates at the MDR

The new EU Medical Devices Directive (MDR) affects everyone and there are only a few months left before important transition periods for the certification of medical devices expire for manufacturers. This showcase shows you how to successfully implement MDR in simple steps.

Swiss Medtech Expo 2019

KEYENCE INTERNATIONAL April 15, 2019
Service

Our Service

KEYENCE products are designed to optimize our customers' manufacturing and research processes. Our in-house research and development team continuously develops our product range to meet our customers' high quality standards.

Swiss Medtech Expo 2019

RMS Foundation January 29, 2019
Service

Inorganic analysis of traces by ICP-MS

ICP-MS is an extremely sensitive technique that allows simultaneous quantification of 70 elements down to trace levels in the μg/L or sub-μg/L range, and can therefore handle a large variety of analytical challenges.

Swiss Medtech Expo 2019

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