Cirrus can design and conduct experiments for device performance testing (e.g., catheter, nebulizer, dry powder inhaler) and can recommend a suitable delivery device(s). The work can be conducted under GMP or GLP conditions and QA reviewed, if required, so that the results are ready for inclusion in a regulatory submission. Furthermore, our senior staff, who have many years of industry experience both with device selection and regulatory filing, can provide support with the device regulatory submission.