To answer the question what degree do you need for a career in medical device sales, there is a short-answer and a long-answer to this Read More » Getting Hired The 5 Best Tips For Getting Into Medical Sales If you want to take your career into your own hands and get your foot ...
TÜV SÜD Danmark ApS is the second EU MDR (Regulation (EU) 2017/745) Notified Body under TÜV SÜD. Providing services to medical device manufacturers globally, TÜV SÜD Denmark Medical Health Services‘ primary focus is to deliver a seamless and efficient certification experience by opt...
Company Present in both Europe and North America, GMED’s level of excellence and standards have made it an internationally recognized name in the field of medical device certification. About Us Recognition and Accreditation Leadership Role of Notified Bodies Governance Role of Approved Bodies Choose ...
products specifically intended for the cleaning, disinfection or sterilisation of devices as referred to in Article 1(4) and of those referred to in the first paragraph of this point. Before placing a medical device on the market, manufacturers shall perform a conformity assessment of a medical d...
Certification & Regulation Scalable Solutions Comprehensive Supports Why Hygienic Design Matters? For environments requiring high levels of cleanliness, hygienically-designed medical devices, like ADLINK’s panel computers and monitors, can help reduce device contamination, cleaning effort, and transmission of...
GUC today announced the achievement of highly coveted ISO 13485:2016 certification, which make GUC the first and only ASIC company to meet these demanding standards and will strengthen qualities of medical IC design and manufacturing services.
Innovative global brand with over 90 years of experience in medical equipment manufacturing We assigned Cisema in the past to assist us with our product safety certification for China. Cisema was responsible for gaining approval for our products, supporting us regarding China regulatory affairs, as we...
Our expert maintenance services include preventative and as-needed maintenance for critical care equipment. This ensures maximum device performance and reliability for our clients. As a result, you will have the less administrative burden and will be able to protect the investment of our customers. ...
Information of product (name and certification) and applications for registration and record-filing of medical devices must be included in the purchase inspection record and sales record respectively (Articles 32 and 38); Medical device business enterprises must provide after sales service. If the afte...
Device verification, including a review of technical documentation Quality system audit based onISO 13485, where an INMETRO auditor confirms the manufacturer’s production process’s compliance Witnessed routine production tests conducted on 100% of the products bearing INMETRO certification ...