Expert Insights On Cold Chain
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                    New EU Directive Marks Cybersecurity Regulatory Paradigm Shift For Bio/Pharma & Medical Devices
                        2/15/2023
                    The EU's new Directive 2022/2555 on the Security of Network and Information Systems (“NIS2”) mandates cybersecurity risk management measures and reporting requirements for all segments of our industry, including labs; CROs and CDMOs; and manufacturers of APIs, bio/pharmaceuticals, and medical devices. 
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                    After Decades Of Biomanufacturing Workforce Development, What's Next?
                        2/1/2023
                    We have seen exponential growth of the biotech industry in recent decades. Companies have struggled to find qualified workers. To close that workforce gap, we need to leverage the lessons from successful biomanufacturing training programs and consider new approaches. 
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                    6 Strategies To Protect Your Biologics Supply Chain In 2023
                        1/25/2023
                    Instead of automating everything — which costs a lot and doesn't solve every problem — drug makers should focus on building scalable, need-specific supply chain operations. This article discusses supply chain resilience strategies biotech companies can reasonably control. 
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                    The Holistic Guide To Supply Chain For Cell & Gene Therapy Startups
                        1/19/2023
                    How does the cell and gene therapy supply chain team stay ahead of the expected changes and respond at the speed the developing program expects? Supplier selection, raw materials, built-in quality, warehousing and logistics, and traceability are all covered in this article. 
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                    New Approaches For Drug Substance Freezing And Storage
                        1/12/2023
                    The latest in drug substance-refrigeration technology gives the biopharmaceutical industry options for freezing and storing liquid DS. Here are some insights for optimizing setups based on application, facility, and budget. 
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                    1 Year Out, Where Do We Stand On DSCSA Implementation?
                        11/21/2022
                    This month kicks off the final year of a decade-long process to enhance overall security of the U.S. prescription drug supply chain under the Drug Supply Chain Security Act. This article looks at this year’s DSCSA implementation efforts, before examining where implementation currently stands and what gaps and challenges remain. 
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                    Digital Twins & The CGT Value Chain: A Universe Of Possibilities
                        10/21/2022
                    The cell and gene therapy revolution is coinciding with advanced digital technologies. At the forefront are digital twins, which combine at-scale computing, modeling methods, and IoT connectivity to create full-scale digital replicas of physical assets or real-world processes, such as factories, value chains, and even humans. 
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                    Autonomous Supply Chain Planning Is Within Reach
                        10/19/2022
                    In a fast-paced industry constantly innovating — from personalized medicine to health wearables — life sciences companies must be prepared to adopt transformative technologies that can help them meet the demands of the future of medicine. Autonomous supply chain planning is not science fiction; it's here, and it's now. Building a practical road map will help. 
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                    Attributable Data Integrity in Modern Biopharma Using ALCOA Principles
                        8/29/2022
                    This article is the first in a five-part series providing contemporary, practical, and useful examples of data integrity within each of the five traditional principles of ALCOA. This article centers on A: Attributable. 
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                    The Process Map To Ensure Biopharma Raw Materials Supply
                        8/16/2022
                    In new product introduction, there is often a lack of a basic data package for a product being scaled up for clinical or launch supplies. This can lead to several issues, e.g., capacity and lead time restrictions, oversupply, and more. A stepwise process can be used as a guideline for introducing a material to support new drug substance manufacture. 
