MedtecLIVE is the result of a merger of Medtec Europe and MT-CONNECT. With approximately 350 exhibitors it is Europe’s second-largest exhibition for medical technology.
From 21 May to 23 May 2019, MEDICRO will be participating as a direct exhibitor at the MedtecLIVE, which will take place at the Exhibition Centre Nuremberg, Germany. You can meet us in hall 10, exhibition stand 10.0-613, directly opposite the Exhibition forum. Take the opportunity to join our magician Markus Billner on a magic journey and get to know MEDICRO’s competences in the fields of clinical trials, PMCF studies, clinical evaluations, regulatory consulting and translations for the medical technology industry afterwards. Simply contact us and be our guest at the MedtecLIVE! We look forward to meeting you there.
For nearly 20 years we have been assisting companies in all areas of study organization, marketing authorization, medical writing, translations and any regulatory matters as a strong and reliable partner in medical technology, biotechnology and the pharmaceutical industry.
MEDICRO is a contract research organization and consulting company located in the Nuremberg Metropolitan Region, operating worldwide. It is our goal to convince you through cost efficient services, profound knowledge and quick response times. Years of cooperation with satisfied customers show that high quality standards pay off for both sides.
- Innovative – MEDICRO is your innovative partner in clinical trials and PMCF studies!
- Focused – Your wish is our concern! We achieve highest quality through motivation and dedication.
- Efficient – Your study, your clinical evaluation, your regulatory matters or your translation –performed by us efficiently!
Your Needs and Expectations
If you expect highest quality and best services for your projects, then MEDICRO is the right partner for you. In particular regarding the transition to the MDR, a quick implementation, compliance with requirements, on-schedule execution and a reliable and professional partner is what is important to you. We provide advice in all matters relating to the MDR.
Take the chance to meet us in person here in Nuremberg. Be captivated by a brief moment experiencing the Magical Touch, and afterwards get convinced of our expertise. MEDICRO is your partner who consults, assists and acts in your interest.
Clinical Trials / PMCF Studies
You are conducting a clinical trial, an RCT or PMCF study? MEDICRO assists you in study planning, budgeting, submissions, during the conduct and data analysis. In due consideration of and complying with the regulations, we always act considerately to achieve the best possible results while observing your budget. Strategic consulting is thus part of our services.
Because of the MDR taking effect, a clinical evaluation or an update thereof will be needed for all medical devices until May 2020. As opposed to other companies, MEDICRO offers on-schedule preparation of clinical evaluations, also for an all-inclusive price if requested.
Placing your product on the market, implementing conformity assessment procedures, adopting and revising quality management and risk management systems and also their review as to being suitable in terms of the MDR – we are your reliable and competent partner. MEDICRO offers high quality consulting in all regulatory matters and develops possible solutions with you.
You need translations of your instructions for use, manuals, brochures, catalogues and labels and shortly also of the UDI database entries of your product. Our qualified and experienced specialist translators at MEDICRO provide accurate translations.