Biosimilar, mAb, ADC, Peptides, ATMPs, Cell and Gene Therapy Characterisation Services

Intertek offers wide range of pharmaceutical services which includes wound care analysis. It belongs to medical devices services category. It includes quantification of level of components (inorganic or organic), loading / dosing studies, in vitro simulated antimicrobial active release studies, competitor ...

Intertek offers wide range of pharmaceutical services which includes x-ray powder diffraction (glp & gmp) for pharmaceuticals. It belongs to pharmaceutical analysis services category. It includes gmp services, stability and pharmaceutical testing, physical characterization techniques for pharmaceutical...

Our pharmaceutical auditing and management services give you a transparent view of your supply chain enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes. Through our shared audit programs, delivered by our global network of specialist audit...

Bioanalytical LC-MSMS and Immunoassays

Biologic Drug Characterisation

Biopharmaceutical and Pharmaceutical CMC Support

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...

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...

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...

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)....

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...

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...

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 

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.