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- Highly customized aptamer discovery solutions for aptamers in neurological disease sector
- Highly customized aptamer discovery solutions for hot areas for aptamers sector
- Wound care management solutions for home health agencies sector
- Wound care management solutions for skilled nursing facilities sector
- Wound care management solutions for hospitals sector
- Wound care management solutions for wound care clinics sector
- Highly customized aptamer discovery solutions for therapeutic aptamers sector
- Microbial Reduction Solutions for Cosmetic and Packaging
- BrightInsight Solutions for Biopharma
- Hip and Knee Replacement Systems for Medical Education
- Solutions for Healthcare
- FluidFM for CRISPR cell line development Accelerate your CRISPR gene editing and cell line engineering
- Single-cell omics with Live-seq
- Mechanobiology and single-cell adhesion measurements with FluidFM
- FluidFM for Neuroscience Pattern, stimulate, inject into, and analyze single neurons
- FluidFM for Virology Study viral entry and replication on a single virion-single cell level
- Software Solutions for Researchers
- IGX Platform Software for Immuno-Oncology
- IGX Platform Software for Cancer Vaccines
- IGX Platform Software for Autoimmunity
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- Excitation-Contraction-Energy (ECE) Coupling Analysis for Cardiac Physiology
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Medical Services Available In Canada Yukon
3,745 services found
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Manufactured by:UP Umweltanalytische Produkte GmbH based inIbbenbüren, GERMANY
We offer turn-key solutions for the measurement of different plantphysiological parameters as well as the related services (installation, launching, maintenance and ...
Manufactured by:EirMed - Trelleborg Healthcare & Medical based inMenomonie, WISCONSIN (USA)
In conjunction with EirMed’s finishing and assembly services, we offer customized device packaging. Each packaging solution is selected to ensure safe and cost effective delivery of your medical devices. EirMed has developed partnerships with sterilization companies to ensure all sterilization requirements are met. Offering a variety of methods from EtO and Gamma to E-Beam and X-Ray, our ...
by:TÜV SÜD America Inc. based inWakefield, MASSACHUSETTS (USA)
In the medical field, practitioners utilize a range of devices to address patient health, from diagnosis to surgery. When the patient comes into contact with a medical device or material, it should fulfill its intended function without harming the patient. Therefore, all medical devices need to undergo a thorough biological risk assessment to protect the patient from any toxic, physiological, ...
by:SRP Environmental, LLC based inShreveport, LOUISIANA (USA)
SRP Environmental LLC specializes in risk evaluation and catastrophe response in hospitals and medical facilities. SRP's Catastrophe Response Team is specifically trained to mitigate risk and reduce liability in healthcare facilities following a fire, wind or water loss. SRP's industrial hygienists are experienced in the special needs of medical facilities including infection control, continuity ...
by:NOVO Engineering based inVista, CALIFORNIA (USA)
NOVO specializes in medical device development services for Class I, II, and III FDA-regulated devices. The scope of our ISO 13485:2016-certified quality management system (QMS) covers a five-phase product development process (PDP) from concept through manufacturing transfer, including support for clinical trials and regulatory submissions. Our medical engineering expertise encompasses both ...
by:ProPlate, operated by Professional Plating Inc. based inAnoka, MINNESOTA (USA)
ProPlate’s dedicated new product development team supports new medical device projects from concept through commericialization through our proven process roadmap. ProPlate® has a library of solutions for a wide range of parts and industries. We are always pleased to take on new challenging projects and expand our Medical Device Silver Plating ...
by:Revanix Biomedical based inCoral Springs, FLORIDA (USA)
Revanix Biomedical's wide selection of dental handpieces repairs are designed to meet all of your dental practice ...
by:Ofni Systems Inc. based inRaleigh, NORTH CAROLINA (USA)
Process, Design, and Equipment Validation are the formal processes for establishing objective evidence that systems consistently produce results or products meeting predetermined specifications, as required by the Federal FD&C Act and cGMP. Validation is an excellent tool to understand and maximize value from your business processes. Validation is also a compliance issue; the FDA requires ...
Manufactured by:Piramal Pharma Solutions (PPS) based inMumbai, INDIA
We offer specialized services in clinical trial supply management using a global network of assets, experience, and expertise in streamlining the clinical trial packaging and supply process, thereby ensuring that the study drug is available as ...
Manufactured by:ZebraSci Inc. based inTemecula, CALIFORNIA (USA)
One of the many variables that contribute to drug delivery device reliability is the primary container itself. With our experience with the containers and components from the world’s leading manufacturers, we can assist you with selecting the right components or optimizing your device to an existing container. Leverage our knowledge, experience and partnerships to be well informed for ...
by:ETLog GmbH based inBerlin, GERMANY
Setting up and support of IC committees. Standard Precautions. Hand ...
Manufactured by:Quantificare Inc. based inSuwanee, GEORGIA (US) (USA)
At QuantifiCare, our project team members come from varied backgrounds in clinical and scientific research. Our qualified staff consist of Imaging Specialists, Project Managers, Data Managers, Trainers, QA Specialists, all working together as a cross-functional team to understand your trial requirements and consult on the latest imaging techniques. We have developed both internal SOPs and ...
Manufactured by:InnoSer Belgie NV based inDiepenbeek, BELGIUM
In vitro and in vivo methods to provide a study setup that thoroughly determines safety and efficacy. ...
by:Lifecore Biomedical, Inc. based inChaska,, MINNESOTA (USA)
Lifecore’s engineering staff works with our formulation and development scientists to transfer or develop a robust process based on customer requirements and good engineering ...
by:Patheon Inc. based inDurham, NORTH CAROLINA (USA)
From initial inquiry through development, manufacturing, testing and product release, quality is paramount. Our in-house quality and validation teams provide a range of assay development, testing, and analytical ...
Manufactured by:Pluristem Therapeutics Inc. based inHaifa, ISRAEL
Graft Versus Host Disease (GvHD) is a potentially lethal complication of hematopoietic cell transplantation (HCT) from a donor. When a patient receives a donor’s stem cells, the transplanted cells may identify the patient’s body as foreign and attack it. The chronic form of GvHD occurs at least 100 days following the transplantation. The GvHD market is predicted to exceed $500 million ...
by:BrightInsight, Inc based inSan Jose, CALIFORNIA (USA)
Leverage our team to develop, configure, or host your next digital health solution. Our digital health subject matter experts, software and quality engineers and UI/UX designers are uniquely trained to develop software with an agile, nimble approach that maintains compliance with privacy, security, regulatory, and quality requirements: Professional digital health services to create and/or ...
by:Source BioScience based inNottingham, UNITED KINGDOM
Source BioScience has access to a COVID-19 Mobile Testing Unit laboratory which can be sited for large volume, fast testing to meet requirements. Whether it is supporters of a sporting event, TV & Film crew/actors needed to be tested, testing at other venues such as theatres, concert venues or televisions studios; Source BioScience is able to offer a tailored solution to meet this ...
by:Vetter based inRavensburg, GERMANY
Learn how we work with you to design a flexible, scalable, reproducible, and efficient manufacturing processes for your clinical ...
by:Vetter based inRavensburg, GERMANY
Our experts provide the guidance, insight, and Vetter process documentation you need to prepare a Common Technical Document (CTD) for clinical trials of your injectable drug ...