The Life Sciences Logistics industry is experiencing significant growth, driven by the increasing complexity of advanced therapies and biologics. It emphasizes real-time visibility, stringent cold chain management, and regulatory compliance (GDP) to ensure product integrity and patient safety. Digital transformation and data integration are key trends.
Total Assets Under Management (AUM)
Pharmaceutical Logistics Market Size in United States
~Approximately 18.5 billion USD
(7-9% CAGR)
- Driven by biopharmaceuticals and clinical trials.
- Increasing demand for temperature-controlled logistics.
- Growth in advanced therapies and personalized medicine.
18.5 billion USD
Blockchain technology offers immutable, transparent, and verifiable records for product lineage and condition, enhancing trust and compliance across the life sciences supply chain.
AI and ML can analyze real-time and historical data from trackers to predict potential supply chain excursions, optimize routes, and improve inventory management for sensitive biologicals.
Integration of IoT sensors directly into packaging allows for continuous, granular monitoring of environmental conditions and location, enhancing product integrity from origin to destination.
The FDA Modernization Act 2.0 (2022) aims to accelerate the development and approval of new drugs and therapies, including advanced therapies, by promoting alternative methods to animal testing and streamlining regulatory processes.
This policy will likely increase the volume and complexity of advanced therapies requiring stringent logistics, creating more demand for Sendum's specialized visibility solutions.
The Drug Supply Chain Security Act (DSCSA) of 2013, with its final enforcement deadline in November 2023, mandates enhanced tracing and verification requirements for prescription drugs throughout the U.S. supply chain, aiming for a fully interoperable electronic system.
This policy significantly increases the need for robust electronic chain of identity and chain of custody solutions, directly aligning with and driving demand for Sendum's offerings.
While not a single '2023' policy, ongoing amendments and guidance under the 21st Century Cures Act continue to promote the development and use of real-world evidence and accelerate approval pathways for regenerative medicine and advanced therapies.
The ongoing focus on accelerating advanced therapy development intensifies the need for precise, real-time logistics and monitoring capabilities that Sendum provides to ensure product integrity from clinical trials to commercialization.
Sign up now and unleash the power of AI for your business growth