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Risk Management Services In Europe
20 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 ...
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. ...
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 ...
by:SCREENTEC based inOulu, FINLAND
Our ISO 13485 and certification supports our growth as a contact manufacturer of medical devices and ...
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. ...
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 ...
by:Apex Healthcare Services Ltd. based inReading, UNITED KINGDOM
We work to support individuals maintain their independence by identifying their support needs and putting in measures to help reduce the risks of them managing their daily tasks on their ...
by:Sage Publications Ltd. based inLondon, UNITED KINGDOM
The American Journal of Medical Quality is focused on keeping readers informed of the resources, processes, and perspectives contributing to health care services. This peer-reviewed journal presents a forum for the exchange of ideas, strategies, and methods in the delivery and management of health ...
by:European Device Solutions Limited based inWhitley Bay, UNITED KINGDOM
We are a leading supplier of Software Quality Assurance and Regulatory Advice to industry and academia with many years’ experience in FDA, EMA, & MHRA regulated life sciences industries in the UK, Ireland, US, Far East and the EU. Our services include the following devices: Medical devices (and accessories), In-vitro diagnostic devices (and accessories), Wellness / lifestyle devices, ...
by:Sectra AB based inLinköping, SWEDEN
Sectra’s enterprise imaging portfolio gives you a unified strategy for all your imaging needs, and lets you improve patient outcome while lowering operational costs. With our solutions, you can reduce the number of systems while providing top-of-the-line diagnostic capabilities spanning both image-intense departments such as radiology, breast imaging, pathology, orthopaedics, and cardiology ...
by:Thermo Fisher Scientific, LIMS & Laboratory Software based inPhiladelphia, PENNSYLVANIA (USA)
Quick to Clinic is an integrated early development offering designed for biotech companies looking for a dependable solution to scale up recombinant antibodies from discovery to first-in-human (FIH) trials. With Quick to Clinic, you balance early development timelines, risks, and future scale-up and commercialization needs. Speed up your early development to as little as 13 months from the start ...
Manufactured by:VTU Group GmbH based inGrambach, AUSTRIA
We support you in developing your standards, in setting up your GMP-compliant production facilities and in establishing the manufacturing ...
by:Almac Group based inCraigavon, UNITED KINGDOM
We are uniquely placed to partner with clients throughout the entire process of CDx Development through our Clinical Trial Diagnostic ...
Manufactured by:Werth Systems GmbH based inHiddenhausen, GERMANY
The pre-installation, localized support and the physical installation to the treatment area. The law regarding health care devices and materials require in depth expertise. A standard office-PC may be installed in a medical environment without thinking further of the consequences. A computer being installed in a operating room or in a intensive care area is a very different process. Lack of ...