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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
- Highly customized aptamer discovery solutions for therapeutic aptamers sector
- Microbial Reduction Solutions for Cosmetic and Packaging
- BrightInsight Solutions for Biopharma
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- 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
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- IGX Platform Software for Autoimmunity
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Medical Services Available In In Afghanistan
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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: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: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 ...
by:InVivo Biosystems based inEugene, OREGON (USA)
The nematode Caenorhabditis elegans is widely used in genetic and biomedical research. DNA fragment insertions can be introduced into the C. elegans genome. Our C. elegans knock-in services include point mutations, floxed alleles, degron tagging, fluorescent tagging and immunotagging. In the past 5 years, InVivo Biosystems has made over 600 fluorescent transgenic lines includuing 15 different ...
by:Bureau Veritas North America, Inc. based inNew York, NEW YORK (USA)
CSA Z180.1-13: The testing package for CSA Z180.1-13 assesses the purity of compressed breathing air supplied to service outlets, and for breathing air systems required to produce, store and distibute such air. This standard package is applicable to compressed breathing air and compressed breathing systems used for supplied-air respirators, supplied air suits, self-contained breathing apparatus ...
Manufactured by:Gentronix Ltd based inCheshire, UNITED KINGDOM
The in vitro micronucleus test (MNT) is a main-stay of most regulatory genotoxicity testing strategies, and is used to detect in vitro clastogens and aneugens. In this regard it complements the Ames test well, as between the two study types they detect all of the three major classes of genotoxin. Fluorescence In Situ Hybridisation (FISH) can also be conducted to differentiate predominantly ...
Manufactured by:Gentronix Ltd based inCheshire, UNITED KINGDOM
The mouse lymphoma assay is one of the mammalian gene mutation assays available and is frequently utilised in most genotoxicity testing regulatory frameworks. Able to detect point mutations, clastogens, and in some cases aneugens; the mouse lymphoma assay has an advantage compared to the HPRT (the alternative mammalian gene mutation assay) due to its capability to detect a broader spectrum of ...
Manufactured by:MedGenome Inc. based inCounty of New Castle, DELAWARE (USA)
Single cell analysis has become a gold standard application in both basic as well as translational research. Several approaches are now available that capture the maximal transcript diversity in a given cell and allowing for multi-model analysis strategies to generate meaningful insights. MedGenome has adopted several commercially available platforms for single cell ...
Manufactured by:MedGenome Inc. based inCounty of New Castle, DELAWARE (USA)
It is estimated that there are approximately 1010–1011 B cells in a human adult. A BCR is composed of two identical heavy chains generated by recombination of V, D and J segments and two identical light chains generated by recombination of V and J segments. Human BCRs undergo recombination at these variable regions, generating a large diverse receptor profile for each cell. Utilizing ...
by:Sage Publications Ltd. based inLondon, UNITED KINGDOM
AADE in Practice, an official publication of the American Association of Diabetes Educators (AADE), is a bi-monthly, peer-reviewed practice journal that combines the heart, art and science of diabetes self-management education. Intended to inspire, inform and empower AADE members and diabetes educators in the field, AADE in Practice publishes practical tools and strategies that directly ...