Supply Chain Auditing
Product Description
Intertek Analytical Services
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GB
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2015On CPHI since
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4Certificates
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1000 - 4999Employees
Company types
Primary activities
Categories
Intertek Analytical Services
-
GB
-
2015On CPHI since
-
4Certificates
-
1000 - 4999Employees
Company types
Primary activities
More Products from Intertek Analytical Services (99)
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Product Nebulised Drug Product Development Services
We have been supporting clients’ product development for over 30 years across all classes of inhaled and nasal delivery technologies including nebulized therapeutics. We provide expert OINDP formulation development, product performance testing and analysis, in vitro bioequivalence studies, stability, produ... -
Product Nitrosamine Impurity Testing
At Intertek we also offer a GC-MS/MS approach which has allowed our experts to achieve excellent LOD and LOQ values. Overall, GC has proved extremely useful for some difficult projects, helping us to present an alternative and successful route to avoiding challenges associated with Liquid Chromatography co... -
Product Pharmaceutical Analysis Contract Services
Whilst your organisation focuses on your core business goals, you will need to select a contract analytical services partner with a strong history of delivering regulatory compliant testing to a consistently high standard. Our contract analysis services are focused on supporting product development, GMP ma... -
Product Pharmaceutical Dissolution Testing
Pharmaceutical dissolution testing plays a key role in drug development and across the drug product lifecycle. In early phase development, dissolution helps to establish the dissolution mechanism, in later stages (stage II to III) dissolution testing helps to drive insight into key formulation or process p... -
Product Pharmaceutical Impurity Analysis and Identification Testing
Our GMP compliant laboratories provide pharmaceutical impurity testing for new drug substances (ICH Q3A(R2)) and new drug products (ICH Q3B(R2)) that can support your product development from an early stage and across the lifecycle of your drug product. Our scientists are adept at method routinely overcome... -
Product Residual Solvents and Organic Volatile Impurities (OVI) Analysis
Our pharmaceutical impurities analysis team provide expert determination and identification of residual solvents, delivered from our GMP compliant laboratories, to help you to ensure that residual solvents have been reduced to acceptable levels in drug products, drug substances and excipients. Often it is ... -
Product USP 232 and 233 Pharmaceutical Elemental Impurity Testing
Your USP Chapter 232/233 Testing Partner
We offer expert GMP elemental impurity analysis services according to USP General Chapter <232> and USP Chapter <233> which are Good Manufacturing Practice (GMP) compliant and are conducted in accordance with these USP chapters to support your raw ... -
Product Vaccine Characterization, Delivery and Bioanalytical Support
Our vaccines development experts provide a suite of services supporting the analysis, delivery, quality control of process and batch release samples and stability studies. We have support the development of a range of vaccines including mRNA, protein, glycoprotein, DNA, carbohydrate, lipopolysaccharide, li... -
Product Intertek Pharmaceutical Services
Intertek's pharmaceutical contract laboratory services, regulatory assistance, and supply chain assurance deliver quality and safety to meet your unique pharma and biopharma outsourcing needs. We bring quality and safety to life!
With our pharmaceutical experts working with you at every ... -
Product Biopharmaceutical Characterisation and Testing Services
Characterization and testing of biopharmaceuticals: Using our expert's insight into a biologic's structure, physicochemical properties, potency, and impurity profile, we help you meet your development milestones.
A range of expertise is available, including assessment of structure... -
Product Pharmaceutical Auditing Services
Auditing services for the pharmaceutical industry: Our pharmaceutical audits are conducted in accordance with the relevant regulatory texts or standards, including GMP, GDP, GLP, GCP, and GVP. We also audit against IPEC guidelines for Pharmaceutical excipients, ISO 22716 (Cosmetics — Good Manufactu... -
Product Inhalation Drug Product Development Services
Services for the development of inhalation drugs: Our team have over 30 years of experience supporting our clients' product development for orally inhaled or nasal drug products (OINDP). This includes formulation, stability, testing, product performance testing, in vitro bioequivalence studies, CMC...
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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