Thermo Fisher Scientific Expands Direct-to-Patient Clinical Trials Service Offerings
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- Pharmacy-to-Patient?and?Depot-to-Patient?services enable centralized control and simplified supply chain planning in managing high-value or limited supply agents available in all 50 U.S. states. Investigational Medicinal Products (IMP) and non-IMP drugs are shipped directly to patients' homes from either a pharmacy or central depot site using a GMP-compliant clinical supply chain system and coordinated through?Thermo Fisher's?HIPAA- and GDPR-compliant Direct-to-Patient contact center and Patheon Logistics.
- The?Clinical Site-to-Patient?service leverages?Thermo Fisher's?Total Transportation Management capabilities, choosing the best option to deliver the medications directly to patients' homes or study sites enabling maximum patient compliance. Moreover,?Thermo Fisher?offers the ability to ship to 47 countries approved and vetted by our regulatory experts, reducing timelines and cost for study sponsors.
- Through the Direct-to-Patient solutions,?Thermo Fisher?provides expertise across the full supply chain, including support for ancillary sourcing, blinding, patient kit production, clinical supply optimization and decentralized clinical trial setups.
- For patients participating in hybrid or virtual trials,?Thermo Fisher?provides additional services such as coordination with home nurses.
- Direct-to-Patient also offers end-to-end cold chain management and traceability and centralized storage of clinical trial material, reducing waste and minimizing the storage space needed at clinical sites.
Marcia Goff, Thermo Fisher Scientific
+1.508.902.7041
marcia.goff@thermofisher.com Rachel Robbins, Greenough
+1.617.275.6521
rrobbins@greenough.biz SOURCE Thermo Fisher Scientific
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