Yourway, an integrated courier and clinical packager in the global clinical trials supply chain market, and Firma Clinical Research, the niche service provider for patient-centric home healthcare, are joining forces to provide coordinated supply and product deliveries and administration services for virtual/decentralized clinical trials. The collaboration between the two clinical study service providers supports patient retention and compliance, while also helping CROs and sponsors improve the efficiency of clinical trial management.
Yourway and Firma are working together to ensure a seamless process for the delivery of supplies and drugs needed for in-home visits to clinical trial patients. Clinical products and equipment are coordinated to be sent directly to the patient. In addition, collected bodily samples and other materials are shipped from the patient’s home through a courier. In-home patient care is performed by an approved healthcare provider.
This patient-centric approach of Yourway and Firma assures delivery, protocol compliance and data quality. The collaboration between the two companies extends through 2020.
“Yourway has served the biopharma industry for more than two decades, and we are proud to collaborate with Firma Clinical to help improve the patient experience for in-home health visits for clinical trials,” says Gulam Jaffer, President, Yourway. “We offer direct-to-patient and direct-from-patient services globally, including shipments that require ambient to frozen temperatures and controlled substances. These services are making virtual and decentralized clinical trials possible.”
“Firma is committed to the needs of patients, sponsors and healthcare professionals by providing in-home care for clinical trials that often involve investigational products (IP),” says Michael Woods, CEO, Firma Clinical Research. “Firma has completed thousands of home health visits in 45 countries, and about 40 percent include the administration of IPs. We take a patient-centric approach to our services and often work with advocacy groups to collect patient survey data for sponsors.”
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
FDA Grants Ziftomenib with Breakthrough Therapy Designation for NPM1-Mutant Acute Myeloid Leukemia
April 23rd 2024Data from the Phase Ib portion of the KOMET-001 trial showed that the once-daily oral treatment may provide a substantial improvement over available therapies for relapsed/refractory NPM1-mutant acute myeloid leukemia.