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Medical Device Services In Canada
18 services found
by:Activation Laboratories Ltd. based inAncaster, ONTARIO (CANADA)
We provide high-quality analytical testing for the medical device industry including chemical, microbiological studies and materials testing. We use a variety of international methods for testing including ASTM, USP as well as customer supplied methods. Our experienced personnel can provide you with validation and feedback on international standard ...
Manufactured by:Katsan Medical Devices based inIzmir, TURKEY
At Katsan’s production facilities, we are proud to provide our partners with one of the most sought-after types of services in the world – OEM production. By this way, our collaborators can have their own brand and put into practice all ideas about new medical device manufacturing without operating, labor and investment costs. High innovative ...
by:Artron Laboratories Inc. based inBurnaby, BRITISH COLUMBIA (CANADA)
We can provide your company with our products at a wholesale distribution price which you can then rebrand under your own private label, resting assured that you are offering your clients medical devices of the highest ...
Manufactured by:Sotera Health based inBroadview Heights, OHIO (USA)
At Nordion’s Gamma Centre of Excellence in Laval, Quebec, we provide state-of-the-art gamma services to medical device and packaging manufacturers, spice producers and specialty products manufacturers. Non-standard and high-precision Gamma processing. When manufacturers of medical devices, food items, polymers, packaging ...
Manufactured by:Pega Medical Inc. based inLaval, QUEBEC (CANADA)
Regulatory clearance of new medical devices is one of our strengths. Pega Medical Services’ strong technical background, coupled with a solid understanding of US-FDA and Canadian regulatory requirements, has been a key factor in submitting successful pre-market applications. Pega Medical is ISO 13485:2016 and MDSAP ...
by:BSI Consulting based inHerndon, VIRGINIA (USA)
BSI Compliance Navigator is the smart, simple way to manage your regulatory information for Medical Device and In Vitro Diagnostic products with EU, UK and US requirements – helping you to get to market faster and maximize your ...
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:Pega Medical Inc. based inLaval, QUEBEC (CANADA)
If you need to know whether your product meets the national and international regulatory requirements for safety and effectiveness, or how it compares to the competition's products, Pega Medical Services can perform in-vitro biomechanical evaluation of your new product to verify its structural integrity and function, as well as recommend possible modifications. Our technical ...
by:Activation Laboratories Ltd. based inAncaster, ONTARIO (CANADA)
The Life Sciences Division was established in 2003 and has evolved to offer a full suite of developmental, CMC and research services for the Life Science market. Clients include Pharmaceutical, Biotech, NHP, Medical Device and Cosmetic companies world-wide. ...
Manufactured by:Norgen Biotek Corp. based inThorold, ONTARIO (CANADA)
Norgen Biotek is accredited to ISO 15189:2012, emphasizing our commitment to quality in our laboratory and R&D services. Norgen offers a number of laboratory services to the scientific community and for medical device developers and manufacturers including highly competent molecular diagnostic testing for both research purposes and clinical ...
by:Xybion Corporation based inPrinceton, NEW JERSEY (USA)
Xybion has demonstrated expertise validating computer programs for all types of regulated businesses in the energy, transportation, financial services, and life sciences (including FDA-regulated businesses such as pharmaceutical and medical device manufacturers, clinical research organizations, and GLP ...
by:CSA Group based inToronto, ONTARIO (CANADA)
Mitigate the risk of a cyber attack with thorough review and testing of your connected products and systems. Cybercrime damage costs are expected to hit $6 trillion annually by 2021, up from $3 trillion in 2015. IoT devices connect twice as many people that are alive in the world. In 2015, the FBI warned about the dangers of IoT, yet most devices are still ...
Manufactured by:Katsan Medical Devices based inIzmir, TURKEY
As the last step of a new product design Katsan provides its partners with marketing consulting services. Our grafic designers, web designers and marketing team will create and implement marketing strategies of your products. Development and implementation of a strategic marketing plan. Target markets research. Creating a brand of a new product (brand name, logo, slogan, presentation etc.). ...
Manufactured by:Pega Medical Inc. based inLaval, QUEBEC (CANADA)
From initial concept to market and everything in between, Pega Medical’s team will guide you through all the steps of product development. Whether you are a physician with a unique product idea, a start-up company overwhelmed by regulatory requirements or a research center looking to bridge the gap between fundamental research and market ready devices, Pega ...
Manufactured by:Thermo Fisher Scientific based inWaltham, MASSACHUSETTS (USA)
Natural killer (NK) cells are innate lymphocytes that kill virally infected or malignant cells. Unlike T cells, NK cells function in an antigen independent manner, responding to anything they perceive as "non-self", including malignant cells. NK cells are an attractive allogeneic immune modulator, as they have a well-known safety profile and lack the potential to cause graft-vs-host disease, a ...
by:Bureau Veritas North America, Inc. based inNew York, NEW YORK (USA)
What are APIS and should I Be Concerned about Them? Active pharmaceutical ingredients (APIs) are defined as any substance or a mixture of substances that when used in the production of a drug, becomes an active ingredient in the drug product. Unlike most chemical hazards in the workplace for which health effects upon exposure are incidental, the purpose of an API is to have the maximum biological ...
by:NEO MD based inGreat Neck, NEW YORK (USA)
Healthcare Software We Develop, By Target Users. NEOMD delivers healthcare software tailored to a variety of medical specialties, including cancer care, cardiology, allergology, physiotherapy, chronic disease management, mental health management, and more. Healthcare software development services involve designing, developing, testing, and, if required, maintaining healthcare-related ...
by:Activation Laboratories Ltd. based inAncaster, ONTARIO (CANADA)
Our scientists are highly experienced in both implementing client assays and developing them de novo. Our Canadian laboratories undergo routine audits from both regulatory agencies and clients alike. Our In Vitro Assay Service and Cell Based Bioassays Services include ...