Clinical Supply Management Resources

41. A Custom IRT System Facilitates Precision Medicine Studies 1/29/2025

    As the industry continues to embrace personalized medicine, the ability to implement and support an atypical supply chain is crucial.

42. Overcoming Inventory Challenges For A Complex, Global Study 7/14/2022

    Explore how the optimization of Interactive Response Technologies (IRT) settings relieved the burden of managing global supply needs for a CRO customer and clinical sponsor.

43. Safely Transporting Medicines To Patients

    Do pharma companies underestimate supply chain challenges? Much can go wrong when sending a therapy from A to B, but the right collaborations can mitigate risk.

44. The Patient-Centric Clinical Supply Chain For Cell And Gene Therapies 8/1/2022

    This article explores how delivering cell and gene therapies to patients requires new levels of agility, flexibility and innovation in the logistical management of supply. 

45. Data-Driven Adaptive Trials Enhance Safety, Progress, And Economics 7/21/2023

    By offering guidance on optimizing ROI from extensive data collections and various endpoints in clinical studies, learn how IRT technology can enhance the data-driven approach for sponsors.

46. My Worst Nightmare In RSTM: Accidental Unblinding 8/28/2023

    Learn how collaborative efforts from study managers, supply managers, biostatisticians, designers, and clinicians can better protect the blind in clinical trials and prevent accidental unblinding.

47. Adapting Drug Supply Strategies To Modern Study Models 7/15/2024

    Advancements like remote-access drug refrigerators and smart packaging highlight the need for patient-centric trial models that integrate virtual and site-based activities to meet diverse patient needs.

48. RTSM And Clinical Drug Dispensation 7/16/2024

    A pharma company used Signant Health's RTSM solution in a Phase 2 schizophrenia trial to ensure drug availability, maintain study balance, prevent duplicate allocations, and manage returns and destruction of unused drugs.

49. Master Protocol Studies: Technology Considerations For The 'Never Ending' Clinical Trial 1/6/2022

    Since the FDA is now encouraging creativity in trial designs, it is important for all stakeholders to adapt processes to follow the science and ultimately bring medicines to patients, faster. This white paper addresses the complexities that come with these trial designs, and how randomization and trial supply management (RTSM) solutions are critical to run flexible, robust, and quality-driven trials.

50. 5 Ways To Get Ready For IRT Regulatory Inspections 7/31/2025

    Preparing for a regulatory inspection during a clinical trial can be daunting. Learn about the importance of clear roles, audit trails, data integrity, and training, and get recommendations to help.