Clinical Trial Supply Management Service

Start-up activities

Define and optimize packaging design, lead times, clinical, regulatory and technical aspects of upcoming clinical trials.

Define and consolidate an overall supply strategy to ensure adequate and sufficient forecasting of drug product for assigned study or programs.

 IMP supply strategy to ensure adequate and sufficient forecasting of drug product, comparators, and final IMP

Set-up and write core label text documents and coordinate the country label text translation and regulatory approval process.

Monitor IMP inventory quantities and expiry dates.

Present IMP information at Investigator Meetings.

Supply chain optimization

Full visibility of CTS activities

Technical partner for clinical development team

Risk/budget management