Intertek has provided contract pharmaceutical services (GMP analysis, bioanalysis, formulation, consultancy, auditing) from our GLP/GCP/cGMP network for over 25 years. With specialist expertise in inhalation drug development, biopharmaceuticals and nutraceuticals, we provide integrated formulation and analysis packages including method development/validation, formulation, elemental impurities, extractables/leachables, QC analysis and GMP release testing. Through our stability storage network (Europe/US/Australasia), we offer efficient study management, flexible storage conditions and testing capabilities to satisfy all regulatory criteria for real time, accelerated or forced-degradation studies. Our GLP/GCP bioanalysis laboratory services (UK/US) support preclinical and clinical development for small and large molecules. Our regulatory consultants ensure compliance and development strategy planning. Quality drives our business with facilities regularly inspected by the MHRA and FDA.