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Medical Device Assembly Industry Services Available In Taiwan
35 services found
Manufactured by:Cedic S.r.l. based inPeschiera Borromeo (MI), ITALY
Ensuring only the best materials are sourced and sustainable packaging is used, our procurement department has evolved to be highly specialised in procuring for the medical devices industry. Clients can rest assured knowing that we utilise controlled sources from a long-standing network of credible suppliers. Our procurement colleagues also work closely with the many technical experts within ...
Manufactured by:ARCH Medical Solutions Corp. based inScarborough, MAINE (USA)
Amplify shares your commitment to quality and regulatory compliance. We will work alongside your team to produce exceptional results through the regulatory journey. We provide superior solutions by utilizing and maintaining strong partnerships at every step of the process. Meredith May, Director of Consulting at Empirical Technologies, advises on launching safe new medical devices to ...
by:MASTERMELT METAL MANAGEMENT based inSweetwater, TENNESSEE (USA)
Mastermelt Metal Management provides refining services for the medical device industry. We refine guide wires, marker bands, rags, wipes, anti-bacterial silver products, gold coated products. Pt, Pt10Ir, Pt20Ir, Pt10Ni, gold and palladium are our ...
Manufactured by:ASAHI INTECC CO., LTD. based inAichi, JAPAN
With a basic policy of investing at least 10% of net sales into R&D expenses, we continue to develop products while maintaining close ties to the medical ...
Manufactured by:Arrotek based inNorth Attleboro, MASSACHUSETTS (USA)
At NeedleTech we are constantly developing new products for the medical device industry, and prototyping is an essential part of the process. We know launching a new product is a huge commitment for any medical device company and fast turnaround of prototypes is an essential part of this process. Our engineering expertise, equipment, flexible production processes, and R&D lab allow us to ...
Manufactured by:MPE Inc. based inMilwaukee, WISCONSIN (USA)
Quickly and clearly understand if your capital medical equipment or medical device has a viable place in the market. MPE Inc. helps you realize how to turn your idea into life-enhancing technology. In turn, this sets the foundation for successful commercialization by aligning on a strategic product goal. Through our product definition services, we’ll identify feasible pathways to market, ...
by:Emergo by UL based inAustin, TEXAS (USA)
Commercializing your medical device first requires you to obtain registration and approval from regulatory agencies in each country where you plan to sell your device. Device registration requirements can vary significantly from country to country, which can create compliance challenges for companies pursuing multiple-market strategies. Depending on where you plan to sell your device(s), ...
Manufactured by:Schivo based inWaterford, IRELAND
At Schivo, we realise that a quick lead time for the development of prototypes is vital to our customers success. With a dedicated team and facilities to assist at all prototyping stages for your product and operate the highest standard equipment to support our customers from initial prototype manufacturing to product ...
by:Emergo by UL based inAustin, TEXAS (USA)
Medical device regulations in most countries require foreign manufacturers to appoint an in-country representative. Your representative acts as your liaison to regulatory authorities and assists with device registrations and vigilance/adverse event reporting. It’s important to choose a representative who is familiar with the regulatory requirements for your product to act in the best ...
Manufactured by:BioT Medical based inPetach Tikva, ISRAEL
Today when a company launches a medical device to market, both the FDA and the EU MDR may require the company to follow up on the patients that use the device in order to monitor postmarket safety and adverse events. Furthermore, as a device company you'd probably like to know if your device is as effective in the real world as it was during the clinical trial. BioT provides you with the set of ...
Manufactured by:Biorep Technologies, Inc. based inMiami Lakes, FLORIDA (USA)
Before you can bring a critical medical device to market to help enhance – and save – lives, you need to be certain it’s right and ready. Along with a commitment to absolute quality standards, our medical device contract manufacturing offers rigorous process validation. ...
Manufactured by:Shining World Health Care Co., Ltd. based inNew Taipei City, TAIWAN
From clinical demands to product distribution, a medical device contains different elements, including demand clarification, prototyping, tooling, regulatory certification, trail production, etc. We realize that there are many discovered unmet needs in the medical device market that can bring out better outcomes for ...
Manufactured by:Advant Medical based inGalway, IRELAND
Advant Medical is a trusted Contract Manufacturing Partner to Global Medical Device Companies. We have built up considerable expertise over 30 years in medical device contract manufacturing of Class I, II, III ...
by:Protheragen-ING based inNEW YORK (USA)
Medical devices play a crucial role in modern healthcare by aiding in the diagnosis, treatment, and monitoring of various medical conditions. Ensuring the safety, efficacy, and quality of these devices is paramount to protecting patient well-being. This is where Protheragen-ING Lab's medical device services come into play. As a Medical Device GLP Company, We specialize in providing comprehensive ...
by:European Device Solutions Limited based inWhitley Bay, UNITED KINGDOM
The new Medical Device Regulation (MDR) comes into force on the 26th May 2021 replacing the Medical Devices Directive (MDD) and the Active Implantable Medical Devices Directive (AIMDD). The MDR applies to all manufacturers selling medical devices into Europe and requires them to update both their processes and technical documentation to satisfy the new requirements. The MDR introduces greater ...
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 ...
by:Corpbiz Advisors based inNoida, INDIA
Central Drugs Standard Control Organisation is, known as CDSCO, is a regulatory body for the Indian medical devices industry, under the provisions of the Drugs & Cosmetics Rules, 1945 and Drugs & Cosmetics Act, 1940 and it’s the national regulatory body for Indian pharmaceutical and medical devices. Team Corpbiz will assist you in CDSCO Registration or DCGI approval for your ...
Manufactured by:A-Laser Precision Laser Cutting based inMilpitas, CALIFORNIA (USA)
The medical industry presents unique challenges to precision parts manufacturers. Not only are the applications cutting edge, but demanding in terms of traceability, cleanliness, and repeatability. A-Laser has the equipment, experience, and systems in place to provide our customers with the highest quality products in the most reliable and efficient manner possible. A-Laser brings unique ...
by:TÜV Rheinland AG based inKöln, GERMANY
High-quality, active implantable medical devices, such as pacemakers or cochlear implants, give patients new quality of life. EU Directive 90/385/EEC defines the requirements for active implantable medical devices on the European market. As a notified body, we conduct conformity assessments for your active ...
by:Emergo by UL based inAustin, TEXAS (USA)
Regulators in most medical device markets require registrants to meet post-market surveillance (PMS) obligations to maintain compliance. However, PMS rules can vary between different medical device markets, requiring manufacturers to develop tailored rather than one-size-fits-all approaches. With deep expertise in post-market surveillance requirements, Emergo is equipped to act as your compliance ...