We project manage the entire IMP solution so that you can carry out a study with minimal obstacles
Full assistance across the entire span of a clinical supply project Including the provision of project timelines, budgeting assistance, IMPD data, CTA application assistance, technical agreements and medication label designs.
Optimisation of Trial IMP
Optimising the trial IMP solution by considering not only variables of the clinical trial (such as patient population factors) but also quantities, shelf-life, manufacture and stability dependent factors
We build strong relationships and collaborative approaches both with our clients and our pharmaceutical contract manufacturers, which enables comprehensive co-ordination of all contract manufacturing.
GMP, GDP and GCP Compliance
We help ensure GCP, GMP and GDP requirements around the IMP are met from project start to finish.