Intertek Analytical Services
About Intertek Analytical Services
Certifications
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FDA -
GMP -
ISO
Categories
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GB -
2015On CPHI since
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4Certificates
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1000 - 4999Employees
Company types
Primary activities
Contact info
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Intertek Pharmaceutical Services, Hexagon Tower, Crumpsall Vale. off Delaunays Road, M9 8GQ, Manchester, United Kingdom
Meet us at
CPHI Americas 2025
Pennsylvania Convention Center, Philadelphia
20 May 2025 - 22 May 2025
CPHI Frankfurt 2025
Messe, Frankfurt
28 Oct 2025 - 30 Oct 2025
Products from Intertek Analytical Services (100)
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Product Analytical Method Development and Validation Supporting Drug Development
Supporting Your Analytical Method Lifecycle
Intertek offers cost-effective strategic approaches to analytical method lifecycle management, which combines method development, improvement, qualification, validation, method transfer to and from client laboratories, and maintenance related to GMP producti... -
Product Biopharmaceutical Development Support Services
Fundamental to your biopharmaceutical chemistry, manufacturing and controls (CMC) development, you will need detailed analytical characterisation data to satisfy regulatory requirements. Our experts strategically deploy orthogonal protein analysis approaches that address key molecular and biological charac... -
Product cGMP Pharmaceutical Quality Control Testing
QC testing of pharmaceutical raw materials to international pharmacopoeia specifications has become a specialty of Intertek. With our knowledge of analytical chemistry and our vast range of instrumental techniques, we can undertake the vast majority of the chemical tests listed within the international pha... -
Product Cleaning Validation Analysis Support for Pharma Production
Our analytical scientists provide cleaning validation analysis from our GMP compliant laboratories. We ensure that fit-for-purpose analytical methods are specific for the substances being assayed and suitable to detect contaminants at the specified ARL for an appropriate level of cleanliness (sensitivity).... -
Product Elemental Impurities Testing
Our elemental impurities experts and toxicologists can help you to develop a compliance strategy to achieve successful implementation of ICH Q3D requirements. Intertek's GMP laboratory services teams facilitate the process through the design of tailored analytical programs based on wide experience of pharm... -
Product Extractables and Leachables Studies
Regulatory agency expectations are continually evolving with ever more stringent requirements for the evaluation of drug product packaging associated with each new product. Our extractables and leachables scientists based at our GMPscientists conduct E&L analysis studies in accordance with regional g... -
Product Formulation Development Contract Services
Our drug product formulation development teams offer design and optimisation of formulations for powders, capsules, liquids and solids, semi-solids, inhaled, nasal, nebulised, pressurised and topical drug formulations. We provide focused understanding from an early stage of development tailored to your new... -
Product GCP/GLP Bioanalysis Services
In our state-of-the-art facilities, we provide GLP/GCP method development, validation, method transfer, sample analysis and pharmacokinetic and toxicokinetic support, along with automated data collection and reporting systems. Over the past 20 years, we have supported the development of pharmaceuticals, bi... -
Product Genotoxic Pharmaceutical Impurities Analysis
Our GCP/GLP/GMP compliant laboratories provide genotoxic impurity testing services to detect and evaluate the potential of GIs for your API and/or drug substances which can support your product development from an early stage to market release. With scientists who are adept at method development and valida... -
Product GMP and CMC Pharmaceutical Laboratory Services
We provide regulatory-driven, phase-appropriate, CMC laboratory and GMP pharmaceutical laboratory services. Our expertise ensures sufficient information for your Investigational New Drug (IND), Abbreviated New Drug Application (ANDA) and New Drug Application (NDA) filings. This is achieved through analysis... -
Product ICH Pharmaceutical Stability Testing and Storage
With a network of ICH stability storage facilities in the UK, US and Australia, we offer an extensive capacity and a range of conditions including climatic walk-in chambers, cabinets and refrigerated as well as freezer storage, covering all ICH stability conditions. These are fully controlled and monitored... -
Product ICH Stability Testing, Storage & Program Management
Our extensive capabilities cover all ICH conditions (or custom conditions), including climate control walk-in chambers, cabinets, refrigerated and freezer storage that are fully monitored and controlled, with backup units at every location. We have 24-hour alarm systems at all sites with dedicated teams on...
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Intertek Analytical Services Resources (2)
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News Boosting in Vitro Testing for Nasal Drug Products
In Vitro Test Methods for Nasal Drug Products VIDEO: Learn how our Alberta Idealised Nasal Inlet (AINI) capability can deliver enhanced IVBE studies for generics and support the development of novel intranasal products targeting specific nasal regions -
Brochure Brochure - Pharmaceutical Services
Covering our full breadth of contract laboratory services, auditing and regulatory consultancy expertise, this brochures provides a summary of our global capabilities.
Visit www.intertek.com/pharmaceutical for more information.
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