Medical Device Services In Asia & Middle East
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based in INDIA
Medical Device Registration in India is overseen by the CDSCO, under the Directorate General of Health Services in the Ministry of Health & Family Welfare. To get a Medical Device Registration without any hassle, contact ...
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by HingeClinicabased in USA
HingeClinica is a world class partner for Medical Device services. We render End to End Medical device MDR compliance and Regulatory services, Clinical trial, Pharmacovigilance services to Medical Devices industry. Our Medical Device team has extensive experience ...
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based in USA
When materials are to be implanted in patients, quality is of the utmost importance. Failure to meet the rigorous standards of medical device OEMs can have devastating results for patients and their families. Ensuring your materials are made to your specifications and investigating failures promptly and accurately are both critical to ...
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based in INDIA
Medical Device Import License in India is managed by the CDSCO, under the Directorate General of Health Services in the Ministry of Health & Family Welfare. To get a Medical Device Import License without any hassle, contact ...
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Manufactured by SeaskyMedicalbased in CHINA
Medical Device Contract Manufacturing is a procedure in which a medical technology business which has single proprietorship outsources manufacturing to another medical device manufacturing firm. Healthcare contract manufacturing is created in accordance with the OEM’s standards and in accordance with ...
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Manufactured by Chemical Inspection & Regulation Service Limited (CIRS)based in CHINA
Medical Devices and In Vitro Diagnostics Product Regulatory Compliance in China. Pre-market Investigation & Analysis. Medical Devices Registration & Approval. Clinical Trial Consulting. Manufacturing and Distributing License Approval. Quality Assurance & Compliance. Risk Assessment & Management. Customs Clearance. ...
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by NSAI Inc.based in USA
ISO 13485 is a necessary certification for medical device manufacturers. It proves that you have a quality manufacturing process and the management standards in place to maintain high quality. ISO 13485 certification is the first step towards achieving compliance with European, Canadian and other regulatory requirements for medical ...
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Manufactured by ZebraSci Inc.based in USA
As competition and increased regulation drive innovation, collaboration between partnerships in a global environment becomes critical to the success of medical device commercialization. We provide pharma and biopharma leaders with insights to reduce regulatory risk and remain compliant, while evaluating strategic tasks against proven ...
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Manufactured by ZebraSci Inc.based in USA
ZebraSci’s experience in primary container engineering, human factors, and medical device commercialization for auto-injectors, needle safety devices and novel drug-device systems assists organizations in developing combination products – from early concept through commercial launch and post-market ...
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Manufactured by Mingyan Metalbased in CHINA
Medical device manufacturing carries a considerable degree of liability and regulatory oversight. When the needs and laws change, the medical industry frequently needs to innovate and introduce new products. There is a diverse range of medical devices and usage scenarios. Materials in medical ...
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Manufactured by Nanosonics, Inc.based in AUSTRALIA
Traceability is the documentation collected to link medical devices and their reprocessing records with patient use. 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 ...
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Manufactured by BioT Medicalbased in ISRAEL
BioT is an easy-to-integrate cloud-based platform designed to instantly connect medical devices, patients and caregivers to ensure a seamless continuum of ...
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Manufactured by Nanosonics, Inc.based in AUSTRALIA
Disinfection is the process by which microorganisms are destroyed in order to prevent transmission to the next patient via a medical ...
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Manufactured by Inventex Medical LLCbased in USA
Based on our many years of experience and connections in the plastics industry and the medical device marketplace, we can provide assistance in all aspects of product development from market analysis, material selection, manufacturability, and end user ...
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Manufactured by MediPurposebased in USA
The MediPurpose™ Medical Device Innovation division collaborates with medical device inventors and innovators to take new medical devices from concept to commercialization—bringing together financing, proven medical device development methodology and ...
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Manufactured by Shining World Health Care Co., Ltd.based in 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 ...
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Manufactured by Dana Medical Co., Ltd.based in SOUTH KOREA
Acupuncture of various oriental medicines such as hochim, long acupuncture, and smile face At the stage of production, Dana Medical Co., Ltd. is developing its own R&D. Raw materials through the spring maker invented through It is a process of processing into a shape. Acupuncture is inserted into the human body. Because it is a medical ...
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Manufactured by DIERS International GmbHbased in GERMANY
Our competent team of engineers, sport scientists and computer scientists is available for your questions and suggestions. To ensure the quality and precision of your DIERS measuring system, we offer you regular maintance services (according to Medical Device ...
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by HingeClinicabased in USA
HingeClinica providing regulatory consulting services to Pharmaceutical, Biotechnology, and API manufacture and medical ...
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Manufactured by Nanosonics, Inc.based in AUSTRALIA
Earle H. Spaulding recognised a disinfection framework was required since all reusable medical devices cannot be sterilized. The Spaulding Classification met a key unmet need that today still forms the basis of international medical device disinfection ...
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