Pharmaceuticals: Exova's pharmaceutical services team, of over 200 experienced and highly qualified staff, provide GMP compliant contract testing and development services to the pharmaceutical, biotech and medical device industries worldwide. Flexibility, speed and excellent communication help our customers get their products to market faster. Our skilled Project Managers allow us to focus on teamwork whilst delivering unrivalled Customer Service, resulting in many relationships which have lasted for over two decades. Our network of laboratories gives our clients easy access to specialised capabilities and services ranging from analytical testing, method development and validation, pre formulation and formulation development for small molecules and NCE's, small scale manufacturing of clinical trials materials, stability storage studies, as well as bioanalytical and microbiological analyses.
Regulatory services support drug development from formulation through to final dossier submission. Laboratories in the Americas are FDA, Health Canada audited and registered. Laboratories in UK are GMP and GLP accredited by the MHRA. Exova provides API testing as well as finished product batch release testing and operates as "in-house" QC laboratory to a significant number of international pharmaceutical organisations.