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Find out solutions to mitigate the impact from clinicalsupply chain risk and discover how to improve dynamic drug supply forecasting strategies. Join this webinar to learn how supply forecasting and interactive response technology can help biotech companies improve supply planning and distribution while reducing cost and risk.
The company has been ranked in the Business Expansion and Research and Development categories in the Pharmaceutical Technology Excellence Rankings. Key among them has been the extension of Syngene’s research collaboration with leading biotech company Amgen Inc. until 2026. Syngene’s collaboration with Zoetis started in 2011.
IRT solutions help clinical trial sponsors meet the complexities of patient randomization and clinicalsupply management. Therefore, the integrity of an entire clinical trial depends on this technology. For example, most clinical trials now have at least one protocol amendment. “As
Unlike commercial pharmaceutical packaging, the primary consideration in clinical trial packaging is protecting the product quality and reliability for research. Furthermore, the list includes clinicalsupply packaging, as well as labelling, storage, and logistics service providers for drug trial projects.
Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinicalsupply packaging facility in Shiga, Japan.
Supply chain uncertainty is a challenge every clinicalsupply chain manager wrestles with – stemming from increasing product demand and quality, the growing complexity of clinical trial designs and a lack of visibility in the supply chain. Achieving clinicalsupply chain flexibility now and in the future.
Collaboration provides clinical trial sponsors with access to the world’s most efficient clinicalsupply processes using a single contract. As a result, global clinicalsupply and operations teams can now single source their commercial drug requirements by utilizing two best-in-class solution providers.
To learn more about site networks, I invited Christian Burns, President of Elligo (El Eh Go) Health Research and Co-Founder of ClinX, on the show. Christian is a serial entrepreneur, investor, and founder of multiple clinical trial companies, including ClinEdge, BTC Network, and Guidestar Research. To learn more, visit [link].
Veeva connects patients, sites, and sponsors, on a single technology ecosystem to make clinical trials easier and faster. SiteVault gives research sites one place to work with sponsors – to reduce the number of systems and logins used to run clinical trials. I’m particularly excited about Veeva SiteVault.
Avoiding “Customs Chaos” in Clinical Trials Means Working Closely with Your Importer of Record Many global clinical trial shipments get muddled regarding the critical role and responsibilities of the importer of record (IOR) for clinical trials.
Avoiding “Customs Chaos” in Clinical Trials Means Working Closely with Your Importer of Record Many global clinical trial shipments get muddled regarding the critical role and responsibilities of the importer of record (IOR) for clinical trials.
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Based on its leading expertise in antibody, protein and peptide technologies, MorphoSys, together with its partners, has developed and contributed to the development of more than 100 product candidates, of which 27 are currently in clinical development.
In the fast-paced world of clinicalresearch, Randomization and Trial Supply Management (RTSM) systems play a pivotal role in ensuring the success of trials. However, a common challenge is that these systems are often one of the last to be considered in eClinical systems implementation for any particular study.
In the fast-paced world of clinicalresearch, Randomization and Trial Supply Management (RTSM) systems play a pivotal role in ensuring the success of trials. However, a common challenge is that these systems are often one of the last to be considered in eClinical systems implementation for any particular study.
In the fast-paced world of clinicalresearch, Randomization and Trial Supply Management (RTSM) systems play a pivotal role in ensuring the success of trials. However, a common challenge is that these systems are often one of the last to be considered in eClinical systems implementation for any particular study.
Benefits: The benefits of using clinical site monitoring metrics and KPIs are significant and wide-ranging. Enhanced Trial Oversight: These metrics provide a clear, objective snapshot of how each site is performing, allowing sponsors and clinicalresearch organizations (CROs) to maintain optimal oversight of the trial.
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Sairiyo is advancing the clinical development of its lead drug candidate, Cepharanthine, a repurposed and reformulated naturally derived compound for the potential treatment of cancer, neurological, inflammatory and infectious diseases. Research and development efforts will be led by Dr. Paul Van Slyke.
In the fast-paced world of clinicalresearch, Randomization and Trial Supply Management (RTSM) systems play a pivotal role in ensuring the success of trials. However, a common challenge is that these systems are often one of the last to be considered in eClinical systems implementation for any particular study.
This collaboration strengthens Novartis’ ongoing commitment to research and partner with other companies to find and develop treatment options for COVID-19 and make them available around the world as fast as possible.
During the clinical development stage, Molecular Partners will provide clinicalsupply.
Managing Toxicity: Ensuring that supply logistics can accommodate the need for rapid adjustments in treatment due to toxicity or adverse events. How do RTSM systems support compliance with Good Manufacturing Practice (GMP) in clinicalsupply management?
Research suggests that sub-Saharan Africa is expected to see one of the largest global increases in mortality rates caused by non-communicable diseases. The patients exist in Africa, as do the high-quality infrastructure of clinical trial management that are available in any other country or global region.” being African American, 3.4%
Multinational clinical trials dominated the total with 95% at 1,119, compared with 58 for single-country trials – or just under 5%. With many clinical trial participants from Ukraine leaving the country after the outbreak of the war, clinicalresearch organisations (CROs) played a crucial role in ensuring trial continuity.
Clinical trials in the US are undergoing rapid transformation in 2025. Driven by advances in digital technology, regulatory updates and growing emphasis on patient-centric design, sponsors and research organizations are rethinking how studies are designed, conducted and analyzed. billion by 2033, indicating a CAGR of 16.84%.
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