In Vitro (Invitro Toxicity Monitoring) Services Available In Canada
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Manufactured by ImmunoPrecise Antibodies Ltd.based in CANADA
In vitro analytical tools allow for the study of various critical quality attributes like production yield, target- and/or poly-reactivity, colloidal stability, melting temperature, self- and/or cross-interaction, solubility, and fragmentation. IPA is equipped with a state-of-the-art bio-inert HPLC enabling analytical ...
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Manufactured by Piramal Pharma Solutions (PPS)based in INDIA
In vitro facilities at PDS provide absorption, distribution, metabolism, and excretion (ADME) services for faster and improved decision making points or standalone offering to support drug discovery programs. Cost-efficient, standardized and customized assays for ADME parameters are provided to the ...
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Manufactured by Piramal Pharma Solutions (PPS)based in INDIA
Piramal’s in vitro Biology is designed to provide best in class support to our clients to enable their preclinical drug discovery, including assay development, hit identification, hit-to-lead and lead optimization, including HTS, multiplex assay development, primary/secondary functional assays, HCS, and selectivity. Our assay team ...
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Manufactured by CD Formulationbased in USA
In Vitro Dissolution Assay: The dissolution rate test of the drug was determined using an in vitro dissolution assay. For poorly soluble drugs and their oral dosage forms, such as tablets, capsules and suspensions, the dissolution of the drug in the body fluids at the absorption site is the rate-limiting step in drug absorption. Drug ...
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based in GERMANY
For legal manufacturers of in vitro diagnostic devices we offer conformity assessment procedures according to Directive 98/79/EC as a Notified Body (EU Identification Number „0483“).Conformity assessment with the involvement of a Notified Body is mandatory for all manufacturers of products according to Annex II list A and B, as ...
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Manufactured by Creative Bioarraybased in USA
In vitro toxicology and in vitro toxicity testing involves the study and interpretation of adverse effects through in vitro research methods typically associated with bacterial and mammalian cell cultures. Creative Bioarray's in vitro toxicity testing uses the latest advances in the field of in vitro toxicology ...
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Manufactured by Owlstone Medical Ltd.based in UNITED KINGDOM
Headspace VOC analysis of in vitro, ex vivo and biofluid samples. Identify VOC biomarkers relevant to key disease processes through in vitro ...
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Manufactured by Profacgenbased in USA
Protein is an important source of drug development and industrial enzyme preparation. It is important to reduce side effects and improve the physical and biological properties of engineered proteins. Glycosylation is a common modification of proteins. The process of changing the glycosylation to alter the properties of proteins is known as glycoengineering. The importance of glycoengineering in ...
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based in USA
You must comply with the In Vitro Diagnostic Directive (IVDD) 98/79/EC, if you want to market your In Vitro Diagnostic Devices in the EU. As a notified body, accredited to the full scope of IVDD, we can test and certify your medical devices and quality systems. TÜV Rheinland offers a broad range of service for determining ...
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Manufactured by Gentronix Ltdbased in 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 ...
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by Selvita S.A.based in POLAND
Cell and Molecular Biology Department at Selvita performs In vitro comparative studies of biosimilar insulins and insulin analogs as well as battery of various therapeutic antibodies (e.g. TNFα, VEGF and HER2 inhibitors etc.). These studies should be comparative in nature and should be designed to have appropriate sensitivity to ...
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based in USA
PRIMA performs in vitro bioaccessibility tests for lead according to EPA Standard Operating Procedure 9200.2-86. This method uses simulated stomach conditions to measure the amount of lead that may be leached from ingested soil. Soil may be elevated in lead, but if the lead is not bioavailable, then the soil may pose little risk to human ...
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based in GERMANY
In the area of CE marking we cover a wide range of devices under Regulation (EU) 2017/745 on medical devices and 98/79/EC on in vitro diagnostic ...
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Manufactured by Surmodics, Inc.based in USA
Surmodics facilities are ISO 13485:2016 and ISO 9001:2015 certified for design, development, production and distribution of in vitro diagnostic and surface modification technologies. Expect lot-to-lot consistency, reproducibility, and optimal performance from products manufactured by ...
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by Adjuvatisbased in FRANCE
High quality analysis and evaluation package. Complying with quality standards, Adjuvatis is able to supply a complete characterization of i-Particles® formulation. The analytical services include chemical formulation analysis physico-chemical characterization and in vitro and in vivo evaluation. ...
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Manufactured by AB Sciex Pte. Ltdbased in USA
Simplify Service and Maintence of Your Clinical Mass Spec System. All SCIEX Medical Device Service Professionals follow a 4-step training program and are certified (and re-certified every 2 years) on SCIEX in vitro diagnostic instruments as well as all major HPLC ...
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Manufactured by AnaBios Corporationbased in USA
culture can be used as an in-vitro model of chemotherapy-induced peripheral neuropathy. Multiple day treatment of human DRG neuronal cultures by oxaliplatin leads to neuronal ...
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by MtoZ Biolabsbased in USA
structure. MtoZ Biolabs has developed a high-resolution mass spectrometry, coupled with pLink-SS software, to provide our customers with accurate analysis of disulfide bonds and free cysteines. Our sample preparation steps have also been optimized to prevent in vitro exchange of disulfide bonds, and maintain native structure. Application of ...
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Manufactured by CD Formulationbased in USA
The dissolution rate test of the drug was determined using an in vitro dissolution assay. For poorly soluble drugs and their oral dosage forms, such as tablets, capsules and suspensions, the dissolution of the drug in the body fluids at the absorption site is the rate-limiting step in drug absorption. Drug solubility assays provided by ...
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Manufactured by Calbiotech Inc.based in
Calbiotech offers contract manufacturing of cGMP compliant, fully traceable, supply-chain-managed buffers and reagents, providing an economical outsourced alternative from a dependable and stable source. We have been designing, developing and manufacturing custom diagnostic reagents and kits since 1998. We produce in vitro diagnostic ...
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