We have expertise in taking products from proof of concept stage through to registration. With an understanding of the regulatory requirements in NZ, Intuit can ensure a fast and cost-effective route to market.
Intuit partners with a number of pre-clinical and clinical trial providers in NZ who are able to perform trials from early stage to final registration-standard studies, including GLP and GCP studies.
With a background in EU regulatory affairs, Julia can also ensure that trials are suitable for EU registration.
We also offer protocol development and GCP trial monitoring.
Intuit can provide consultancy services for existing products or development projects, or we can simply provide additional flexible regulatory resource when you need it. Contact us to discuss your requirements.
Julia is registered with MPI as an Independent Data Assessor and can assess all aspects of the veterinary medicine dossier, including Chemistry and Manufacturing, Safety, Efficacy and Residues.