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NANOPHARM LTD
NANOPHARM LTD is listed as a small business research supplier in the Scientist.com network, with 2 sites in 1 country and 2 service areas.
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Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Small business
Chemical and Compound Analysis
- Analytical Separations and Purification Analytical Separation and Purification of compound/molecule.
- API Physical Characteristics Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
- Excipient Compatibility Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
- Liquid Chromatography Separate substances using a mobile and stationary phase.
- Size Exclusion Chromatography Separate and identify analytes based on their molecular size.
- Spray Drying Convert a liquid into a powder by rapidly drying the mixture and removing the moisture component.
Chemistry, Manufacturing and Controls (CMC)
- Analytical Development and Validation Request services related to Analytical Development and Validation
- API and drug product storage and release API and drug product storage and release
- API manufacturing process development, tech transfer and validation API manufacturing process development, tech transfer and validation
- API/ Excipients Compatibility Studies Delineate real and possible interactions between potential formulation excipients and the API as an important risk reduction exercise early in formulation development.
- API/DP specific test methods API/DP specific test methods (e.g., stability indicating HPLC assay and purity)
- Chemistry, Manufacturing and Controls (CMC) Request Chemistry, Manufacturing and Controls services
Show all 9 in Chemistry, Manufacturing and Controls (CMC)
- Compendial test methods Run Compendial test methods (e.g., KF)
- Drug Formulation Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
- Integrated Small Molecule Package Process an entire Small Molecule/Compounds Pipeline Project including: Compound Synthesis or Purchase, Compound Analysis/Testing, In Vitro Assays, and Formulation/Reformulation from our bundle of suppliers
Show all 29 services
Clinical Trials
- Pharmacokinetic Studies Design a study that observes the time course of drug absorption, distribution, metabolism, and excretion, as means to test the safety and effective therapeutic management of drugs in an individual patient.
- Statistical Analysis Planning Technical and detailed elaboration of the principal features of the analysis described in the protocol, and includes detailed procedures for executing the statistical analysis of the primary and secondary variables...
Data Science/Bioinformatics
- Discovery In Silico Drug Dynamics Develop In Silico model of a drug candidate with a biological system with applications such as Pro-drug Predictions, ADME-PK Due Diligence, Brain-Barrier Permeability Simulation, Drug Absorption Simulation, In Silico...
Discovery Chemistry
- Method Development and Validation Develop and validate methods for synthesis and scale up of drug candidates.
- USP Testing Analytical Reagents Acquire chemical reagents, solution concentrates and volumetric solutions used to evaluate items in USP testing.
Disease Models
- Respiratory Models Test therapeutic efficacy of drug candidate in respiratory disease model.
Drug Development
- Assay Development Consulting Request consultant services measuring the activity of a drug or biochemical in an organism or organic sample.
- Chemistry, Manufacturing and Controls (CMC) Consulting Consultant services related to the development of pharmaceutical and biopharmaceutical drug products that are consistently effective, safe and high quality for consumers.
In Vitro ADME
- Nasal Permeability Test for passive diffusion and active transport in nasal permeability models.
- Reference Standards Find reference standards for assays, tests and services.
In Vitro Assays
- Assay Development Construct or create new assays or modify existing ones.
- In Vitro Assay Development Develop innovative assay and screening methods outside a living organism to enable a wide range of pre-clinical activities.
Model Development
- In Silico PK-PD Modeling Quantitative modeling and simulations correlation of pharmacokinetic and pharmacodynamic endpoints in support of preclinical and clinical development.
Testing Services
- Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
Service areas:
Where it operates
Sites by country, with the cities in each.
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United Kingdom 2 sites
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Nanopharm Ltd was founded in 2002 by Dr Robert Price and Dr Paul Young specialising in the application of atomic force microscopy (AFM) and other surface sensitive techniques in characterising pharmaceutical materials and formulations. Successful growth of the company has been achieved through an organic business model. In late 2006, with the advent of the cohesive-adhesive balance (CAB™) approach for the characterising active pharmaceutical ingredients (APIs), the company has focussed its attentions on the physico-chemical properties which influence the behaviour of the APIs in terms...
Show the full description
Nanopharm Ltd was founded in 2002 by Dr Robert Price and Dr Paul Young specialising in the application of atomic force microscopy (AFM) and other surface sensitive techniques in characterising pharmaceutical materials and formulations. Successful growth of the company has been achieved through an organic business model.
In late 2006, with the advent of the cohesive-adhesive balance (CAB™) approach for the characterising active pharmaceutical ingredients (APIs), the company has focussed its attentions on the physico-chemical properties which influence the behaviour of the APIs in terms of stability, performance and its influence on the efficacy of the drug product.
This novel development has allowed informed decisions to be made at critical stages during the research and development program, allowing the introduction of possible protection measures and optimisation controls to be introduced earlier into the development process.
- Website
- www.nanopharm.co.uk
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