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Research supplier
Gen-Probe Life Sciences
Gen-Probe Life Sciences is listed as a small business research supplier in the Scientist.com network, with 4 sites in 2 countries and 1 service area.
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Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Small business
Biomarkers
- Biomarker Analytical Validation Assess and optimize the characteristics of a candidate biomarker to ensure reproducibility and consistency.
- Biomarker Clinical Utility Evaluate the potential clinical applications of a candidate biomarker.
- Biomarker Clinical Validation Evaluate the predictive ability of a candidate biomarker for a disorder.
- Biomarker Discovery Identify a biomarker associated with disease progression of disease, effectiveness of therapy or diagnosis of disease or condition.
- Biomarker Services Evaluating normal/abnormal biological conditions and characteristics within the body
- Diagnostic Biomarkers Discovery Identify candidate biomarkers indicative of the presence of a disorder.
Show all 8 in Biomarkers
- Predictive Biomarkers Discovery Identify candidate biomarkers suggestive of a response to a treatment.
- Prognostic Biomarkers Discovery Identify candidate biomarkers representative of disease progression without treatment.
Chemical and Compound Analysis
- API Physical Characteristics Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
- Chemical Stability Measure the stability of small molecules in solution.
- Chiral Separation Purify therapeutically active isomers of drug candidates.
- Dissolution Profiling Measure release of API from formulation (tablet or capsules) under GMP guidelines.
- Electrophoresis Separate nucleic acids or proteins based on physical properties such as charge or mass.
- Endotoxin Testing Use standard assays like LAL (Limulus Amebocyte Lysate), rFC (Recombinant Factor C), or MAT (Monocyte Activation Test) to detect and quantify the level of endotoxins in a sample
Show all 22 in Chemical and Compound Analysis
- Headspace Gas Chromatography Analyze volatile organic compounds (VOCs) partitioned above the liquid/solid phase of a sample.
- Ion Exchange Chromatography Separate and detect analytes.
- Liquid Chromatography Separate substances using a mobile and stationary phase.
- Melting Point Use melting point analysis to characterize compounds based on calorimetry and thermodynamic data.
- NBE RIB 2/5 BA Request information or a price quote for GLP Large Molecule Bioanalysis services and products
- Optical Rotation Distinguish between optical isomers as well as between natural versus man-made compounds.
- Particle Size Analysis Measure particle size distribution and characterize particle size, porosity and composition.
- Partition Coefficient Determine lipophilicity (hydrophobicity) of compounds by measuring log P.
- Photostability Measure drug degradation rates after exposure to various light sources.
- Protein Binding HPLC Uses high pressure liquid chromatography to separate protein-drug complexes.
- Protein Separation and Detection Separate proteins based on properties such as solubility, adsorption or size differences.
- Sample Bioanalysis Determination of concentration of an analyte in biological sample.
- Size Exclusion Chromatography Separate and identify analytes based on their molecular size.
- Solubility Studies Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
- UV-Spectroscopy Conduct sample analysis based on light absorption and transmission.
- Viscosity Testing Evaluate the fluid flow properties of liquids for product evaluation and quality control.
Show all 61 services
Chemical and Compound Testing
- Batch Release Request information or a price quote for Batch Release services
- Limulus Amebocyte Lysate (LAL) Test Detect bacterial endotoxins in raw materials used for the production of cosmetics products.
- USP <2021> Microbial Enumeration Tests Estimate the total aerobic microbial count, total combined yeast and mold counts, and the presence of bile-tolerant gram-negative bacteria present in nutritional supplements.
- USP <2022> Microbiological Procedures for Absence of Specified Microorganisms Determine the absence of objectionable organisms in nutritional supplements.
Chemistry, Manufacturing and Controls (CMC)
- Drug Product Stability Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
- Fill and Finish Processing Confirm final product sterility, formulation and packaging in the biopharmaceutical process.
- Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
Clinical Consulting
- Biomarker Services Consulting Expert advice to conduct solutions for evaluating normal/abnormal biological conditions and characteristics within the body.
Discovery Chemistry
- LCMS Analysis Physically separate substances using liquid chromatography and mass spectrometry.
- Method Development and Validation Develop and validate methods for synthesis and scale up of drug candidates.
- UV and IR Profiling Analyze the integrity of a compound or large biomolecule.
DNA & RNA
- Capillary Electrophoresis Separate ng quantities of DNA to single base resolution.
- DNA Extraction Extract DNA from an original source.
- Genotyping Examine a DNA sequence to identify specific genetic varients .
- Methylation Analysis Determine genomic methylation patterns and analyze methylation in tumors and treated samples.
- qPCR Analysis Measure the accumulation of PCR products in real time.
- Quantitative RT PCR Use quantitative reverse transcription polymerase chain reaction to measure absolute and relative mRNA abundance.
Show all 10 in DNA & RNA
- RNA Extraction Isolate total RNA or mRNA from cells or tissues
- RNA Services Whether you’re isolating total RNA for whole genome expression analysis by microarray or setting up high content screening by s...
- Sanger Sequencing Sequence single strand DNA fragments using DNA Polymerase.
- SNP Characterization Identify single nucleotide polymorphisms to make genetic associations, analyze disease SNPs and determine LOH.
Food Safety & Regulations
- Water Activity Determine water activity in consumer healthcare products involving a USP or FCC monograph.
In Vitro Assays
- Microbiology Study microbes and their role in human health.
Product Orders
- BioTx General Biotherapeutics analyze therapeutics and drugs via biological means and recombinant DNA. Pre-clinical sample bioanalysis and le...
Scientific Data Services
- Bioinformatics Bioinformatics is a powerful method of storing, retrieving and analyzing biological data.
Testing Services
- Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
- Freeze-Thaw Testing Use freeze-thaw cycling to measure the long-term durability of cosumer products.
- Real-time Stability Test Assure stability and physical integrity of consumer products in real-time conditions.
- USP <61> Microbial Limits Test Determine whether a substance or preparation complies with an established specification for microbiological quality.
- USP <62> Microbial Limits Test Determine the presence or absence of specific microorganisms.
Other services
- New Request
Service areas:
Where it operates
Sites by country, with the cities in each.
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United Kingdom 3 sites
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United States 1 site
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Tepnel Pharma Services is an independent Contract Research Organisation which supports the drug development pipeline at the Rx/Dx interface. With over 30 years of experience in supporting pharmaceutical, biopharmaceutical and biotechnology companies through the provision of outsourced cGMP compliant Chemistry, Manufacturing and Control (CMC) and human genetics testing, Tepnel Pharma Services is positioned to provide CMC support for drug development, whilst also providing a companion diagnostic solution which addresses the requirements of personalised and stratified medicines. Specialties...
Show the full description
Tepnel Pharma Services is an independent Contract Research Organisation which supports the drug development pipeline at the Rx/Dx interface.
With over 30 years of experience in supporting pharmaceutical, biopharmaceutical and biotechnology companies through the provision of outsourced cGMP compliant Chemistry, Manufacturing and Control (CMC) and human genetics testing, Tepnel Pharma Services is positioned to provide CMC support for drug development, whilst also providing a companion diagnostic solution which addresses the requirements of personalised and stratified medicines.
Specialties
Research & Clinical Services, CDx Development, Batch & Product Release, Stability/Raw Materials Testing, Method Dev & Validation, DNA Extraction, Microarray Services, qPCR Next Gen Sequencing, Rx Dx Partnership, Small & Large Molecule, Translational, Biomarkers
Under inspection and approval of the MHRA and FDA, our pharmaceutical testing and molecular genetic services include:
•Molecular Genetic Services – full range of services for biomarker discovery, assay development, assay validation and companion diagnostics development in support of R&D, clinical and personalised medicine studies.
•cGMP Drug Development Support Services – regulatory compliant laboratory services that deliver on the promise of quality, scientific expertise and turn-around time according to your developmental needs.
Molecular Genetic Services
Molecular Genetic Services Service Overview
As a Molecular Genetic Services provider, we offer a full range of services for biomarker discovery, assay development, assay validation and companion diagnostics development in support of pre-clinical, clinical and personalised medicine studies. We offer a complete biomarker discovery and validation package from initial study design through to companion diagnostics development.
Our Molecular Genetic Services include gene expression, genotyping, copy number and epigenetic analysis using microarrays, qPCR, Sanger sequencing, fragment analysis and next generation sequencing. All our services can be run as “research use only” or as a regulatory compliant service.
We can support all stages of the companion diagnostics development process including design control, kit manufacture, validation studies and production.
cGMP Services
cGMP Services Service Overview
Tepnel Pharma Services specialises in the provision of pharmaceutical testing in support of drug development. Our cGMP pharmaceutical testing facilities are located in Scotland and are configured to ensure maximum efficiency from sample receipt through to report delivery. With over 30 years’ CRO experience of pharmaceutical testing, we provide regulatory compliant analytics in support of both small and large molecule APIs and finished products. Our staff are committed to continuous development of value proposals on behalf of our clients.
- Website
- www.tepnelpharmaservices.com
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