THE MEDI-GLOBE GROUP IS ON EXPANSION COURSE IN CHINA
The Medi-Globe Group is dedicated to developing and marketing innovative state-of-the-art medical diagnostic and treatment solutions. Around the globe, our products ease the work of physicians and as a result benefit our patients.
In Gastroenterology, Urology and Pulmonology, the Medi-Globe Group enables medical professionals to treat patients with high-quality medical technology for minimally invasive therapies. We provide products and systems that continuously improve both efficiency and high-quality results. Our business ethics commit us to the highest level of responsible ecological, social and economic business practices.
We take our responsibility for developing, manufacturing and marketing instruments for the benefit of patients seriously. In doing so, we strive to sustain and measurably improve the quality and performance of our products, services, and processes.
Our Quality Management (QM) monitors compliance with relevant national, European and international standards and regulations for the development, manufacture and placing on the market of our instruments. In addition, our QM department continuously monitors standardized workflows and processes in all departments and corporate production sites to ensure, among other things, the highest level of product quality.
Based on user feedback and market observations of our sales structures, QM assesses the necessary measures to optimize products and processes.
Medi-Globe routinely conducts audits at our suppliers‘ facilities to ensure that raw materials and components are always delivered and manufactured to the agreed specifications.
Medi-Globe is currently taking the necessary measures to meet the requirements of the upcoming MDR.
In addition to being ISO 13485:2016 certified, all our products bear the CE mark. Furthermore, we operate in full compliance with Good Manufacturing Practices (GMPs) and all requirements of international health systems such as, but not limited to, the US Food & Drug Administration (FDA), the Canadian Medical Device Regulations (CMDR), and the Japanese Pharmaceutical Affairs Law (JPAL).
Our first responsibility is with physicians, nurses and patients. Everything we do for them is of the highest quality. We also take full responsibility for our employees worldwide and treat everyone with dignity and respect.
Our SPIRIT of Innovation best describes what we stand for.
Alte Huenxer Straße 115
753 01 Hranice
Asept InMed SAS
9 Avenue Mercure
3526 KV Utrecht
Medi-Globe Brasil Ltda.
Av. do Contorno, 2090
– sala 201 E 202 –
UROTECH GmbH, organizační složka
602 00 Brno
Medi-Globe Group Representation Office APAC
26/F, Two Harbour Square, 180 Wai Yip St, Kwun Tong, Hong Kong
Medi-Globe-Strasse 1 – 5
83101 Rohrdorf OT Achenmühle
Ⓒ Medi-Globe GmbH. All rights reserved.