Breakthrough Cellular Therapy Solutions
Cellular therapy and regenerative medicine are burgeoning fields within healthcare showing tremendous promise in the treatment of a wide range of serious conditions. Unlike donated tissues and organs, which are in limited supply, stem cells offer the possibility of a renewable source of replacement cells and tissue. The use of cord blood and adult stem cells is revolutionizing the treatment of everything from Parkinson's disease and ALS to spinal cord injuries, burns, heart disease, diabetes and arthritis. Already, more than 80 diseases and disorders can be treated using cellular therapy. The potential available through ongoing research is astonishing.
As these treatment options and research programs continue to emerge and proliferate, so too does the need for a single, specialized system that fully integrates all of the complex components of cellular therapy — from donor registration and product management through patient education and care to outcomes management and reporting. With Mediware’s strong history of leadership in blood and biologics management, the natural expansion of cellular therapy solutions is a simple one.
Our Transtem™ solution brings a comprehensive platform of cellular therapy management to the industry. With a sharp focus on positive patient outcomes, ongoing cellular therapy research and development as well as compliance with emerging regulatory trends and standards, this innovative suite of two software applications supports the entire process. Plus, its comprehensive quality improvement features set the stage for a true partnership in research, fusing technology and medicine for a safer patient experience and better outcomes.
Transtem’s simple, Web-based interface means easy, intuitive navigation for your donors, patients and clinicians. That means better communication and improved data sharing and integrity across the entire care process.
Collection, Lab and Product Management
Developed by clinicians using a knowledgebase refined over years of practical use in both clinical and research environments, Transtem's powerful lab and product management software bridges donor, clinician, product and patient information into a single, easy-to-use platform. Its rich, interactive — and extremely donor friendly — tools give donors easy access to online screening and educational materials complete with convenient access to the donor questionnaire. An easy-to-use collector’s portal means clinicians are always just clicks away from the necessary training and education they need.
Plus, Transtem’s built-in GMP and regulatory compliance controls automate and streamline product collection, manufacturing and storage processes for the highest level of safety and security. Integrated patient information provides critical outcomes management and reporting details so you can easily and seamlessly track treatment results.
Under even the best circumstances, managing the care of patients across islands of data is a challenging endeavor. But, when it comes to complex treatment involving cellular therapy and transplant medicine, you simply can’t afford to have critical patient data housed in outlying systems. Transtem's patient care software integrates and streamlines all aspects of patient care from clinical data management to administrative functions to patient and family education and so much more — into a single system. With this solution, you can easily receive, review, store and share information back and forth, in real-time, with referring clinicians, hospitals, ancillary service providers or anyone else involved in patient care.
Comprehensive patient and family education features create well informed, aware patients and help take the fear out of treatment. Powerful bedside charting tools, continuing care management roadmaps and remote patient monitoring options combined with integrated outcomes management and reporting features enable you to track patient progress before, during and after treatment. So you have a holistic view of patient care and outcomes. Plus, Transtem is designed to not only adhere to, but maximize, the standards established by CIBMTR, ASMT and other regulatory or policymaking bodies.