Refine by
Risk Management Services Available In In Denmark
41 services found
by:HOSPINORM Projects GmbH based inDubai, UNITED ARAB EMIRATES
Financial Services from Hospinorm combines in-depth industry know-how. financial expertise and extensive risk management experience to ensure that both communities and developers benefit from investment of critical infrastructure ...
Manufactured by:Intelesens Ltd based inBelfast, UNITED KINGDOM
At Intelesens, we conduct periodic reviews of our quality management system and monitor the implementation and effectiveness of quality plans. We implement and maintain a risk management approach in the processes of the Quality System and in the life cycle of products. Our pursuit of our quality standards and operational procedures are clearly ...
Manufactured by:RSD Engineering Solutions SL based inCanovelles, SPAIN
RSDis in charge of complex projects, including the ones following the ATEX normative for pharmaceutical industries. We manage and lead the projects in their totality: planning/costs/quality/risk management/… According to us, it is essential that the relationship with the customer has to be based on confidence. That’s why we propose a ...
Manufactured by:Cedic S.r.l. based inPeschiera Borromeo (MI), ITALY
Our Quality Management System (QMS) complies with ISO 13485 standard and is MDSAP certified for Australia, Brazil, Canada, the United States and Japan. Patient safety is guaranteed through product CE certifications, FDA clearance and compliance with the applicable ISO standards , such as ISO 14971 for conducting Risk Management. ...
by:European Device Solutions Limited based inWhitley Bay, UNITED KINGDOM
We have worked with numerous SMEs and Start Ups to develop their Quality Management System (QMS), Technical File and Risk Management Documentation to help them attain a CE Mark for their new medical device(s) in both a timely and cost-effective manner. We have experience of working with all classes of medical device (Class I, IIa, IIb and III) ...
Manufactured by:FORCE Technology based inBrøndby, DENMARK
It is a determining factor that you begin the process correctly and consider legal requirements for product and quality management, from the beginning of the development phase. To be able to meet the different test standards within EN 60601 or IEC 60601 family, you must be able to document product development according to standardized risk ...
by:Constellis based inReston, VIRGINIA (USA)
The ongoing COVID-19 pandemic has created critical issues for governments and businesses across the globe, from dealing with the spread of the virus to disruption and economic impact. In response to this crisis, Constellis offers a fully integrated risk management solution that includes protective measures to keep the outbreak from overwhelming hospitals and ...
by:American Risk Management Resources Network, LLC (ARMR.Network) based inMiddleton, WISCONSIN (USA)
Improper disposal of medical records-A restoration firm entered a medical facility after a significant water event. While collecting all wet documents, the employee of the firm took wet medical records and simply disposed of them in the trash. This became a claim because for the failure to properly destroy personal ...
Manufactured by:Integer Holdings Corporation based inPlano, TENNESSEE (USA)
Our commitment to quality ensures that our products and services meet or exceed the highest standards set by the United States Food and Drug Administration (FDA), the European Community, and other internationally recognized agencies. We maintain an industry-wide reputation as an award-winning manufacturer with high quality standards through enforcement of stringent clinical and regulatory ...
Manufactured by:Nanosonics, Inc. based inSydney, AUSTRALIA
This process is essential for investigations in the event of reprocessing failures, outbreaks or recalls, and can help facilities manage risk. Traceability is required for semi-critical and critical medical devices that undergo HLD or sterilization. ...
by:Custom Medical based inDarmstadt, GERMANY
In the MDR, the word usability or usability in the German form occurs only twice. However, there are requirements on the subject of usability in many different places in the guideline. At at least 10 places requirements are made to the product and the manufacturer, which can be fulfilled only with a useful Usability engineering process. ...
by:Integro Insurance Brokers based inNew York, ILLINOIS (USA)
We’re known for our expertise and passion in delivering exceptional brokerage and consulting services to the healthcare industry. Our healthcare team listens to your concerns, addresses your needs, and helps you meet your risk financing objectives. ...
Manufactured by:Ortho Clinical Diagnostics based in, SINGAPORE
Tap Into The Mind Of Your Lab With Insights That Enable Your Decisions To Be Made With Greater Ease And Confidence – Informed By Data Solutions That Encompass And Address All Aspects Of Your Lab. ...
Manufactured by:Novasep based inChasse-sur-Rhône, FRANCE
We believe that the quality and transparency of communication with you and within our organization are crucial in delivering your project. Each project is attributed to a professional project manager who is your dedicated point of contact at Novasep for the whole duration of the collaboration. The project manager coordinates all activities related to your projects and liaises between the ...
Manufactured by:Ecomed Solutions based inMundelein, ILLINOIS (USA)
Many clients face internal challenges such as limited resources, capabilities, or internal bureaucracy and risk falling behind their ...
by:SCREENTEC based inOulu, FINLAND
Our ISO 13485 and certification supports our growth as a contact manufacturer of medical devices and ...
by:Clearwater Security & Compliance LLC based inNashville, TENNESSEE (USA)
Clearwater’s ClearAdvantage managed services program transforms a cumbersome cost center into a business asset and competitive differentiator. A Unique, Comprehensive Cybersecurity and Compliance Managed Services Program. Managing complex cybersecurity and compliance operations can be difficult, if not impossible if you don’t have the required expertise or resources. Whether in the ...
by:sfm medical devices GmbH based inWaechtersbach, GERMANY
On the way to the successful marketing of our OEM products, we take care of all the necessary conformity certifications: In coordination with our customers and from one source. ...
by:Bureau Veritas North America, Inc. based inNew York, NEW YORK (USA)
Meeting legislative regulations and customer requirements for the manufacture and sale of medical devices in a global marketplace can be confusing. With so many regulations, differing from country to country, an organization must address a complex array of quality, process, and management issues in order to compete ...
Manufactured by:ProBioGen AG based inBerlin, GERMANY
Customer satisfaction is at the heart of our quality management system (QMS), which assures products and services of utmost quality. We place the highest priority on product integrity, safe GMP manufacturing, and regulatory compliance (EMA, FDA, ICH). Our best-in-class QMS is founded on state-of-the-art technologies for manufacturing and testing. It is operated by a highly educated and ...