Pharmaceutical Testing and Services
Our pharmaceutical laboratories provide contract pharmaceutical services to the highest industry standards.
Exova compliant with best industry practice
We offer a friendly but professional approach, essential when building long term productive partnerships. We are an ethical, independent company, offering a confidential service to our customers.
Our laboratories are compliant with industry standards, operating to cGMP guidelines and have been audited by the MHRA (Medicines and Healthcare products Regulatory Agency) and/or the FDA (US Food and Drug Administration).
Our services range from formulation services, method development, stability storage and batch release testing, servicing all sectors of the pharmaceutical and related industries.
Services are offered worldwide from our UK and Americas laboratories.
Pharmaceutical and Testing Services
Batch Release Testing is a critical step required to release vital medicines to market. We have a wide range of analytical capabilities to enable the release of products to stringent cGMP guidelines.
We can offer a ‘one-off’ service for analysis or method development; or a longer term, ongoing service for routine batch analysis and assessment of material for batch to batch consistency throughout a manufacturing campaign.
We provide clinical supplies areas which operate to good manufacturing practice and specialise in GMP manufacture and supply of investigational medicinal products for early phase clinical studies.
Our analytical capabilities are available to characterize your raw materials, determine changes in materials due to fabrication processes or sterilization, or investigate the reasons for product failures.
We have extensive experience in the development of analytical methods for pharmaceutical drug substances and products. We routinely work on a wide range of formulation types and on projects.
Exova offers comprehensive particle size testing for the characterisation of fine particles.
Our pre-formulation expertise enables us to work closely with our clients’ discovery functions. Formulation expertise includes development of a wide variety of dosage forms appropriate for clinical trials, commercialisation and line extensions.
We provide a range of standard and customized analyses for pharmaceutical raw materials and intermediates.
Our regulatory consulting services assist our clients in their development projects, specialising in work with a high chemistry and pharmacy content.
The company offers a full range of monitored ICH temperature, humidity and light stability storage conditions. We also have the flexibility to store samples at other temperatures for degradation studies/accelerated storage, or frozen for biologicals.
We provide the industry with technical consulting services to support the development of new products or the investigation of existing products and processes for the pharmaceutical, personal care and consumer product sectors.