Clinical Supply Regulation Research 
XTalks
APRIL 6, 2023
IRT solutions help clinical trial sponsors meet the complexities of patient randomization and clinical supply management. He also shared how modern software development concepts are impacting IRT platforms and transforming the user experience in clinical trials.
Pharmaceutical Technology
MARCH 20, 2023
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%
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Imperical Blog
SEPTEMBER 7, 2023
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.
Imperical Blog
SEPTEMBER 7, 2023
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.
The Pharma Data
JANUARY 10, 2021
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. For more information, please contact: SOURCE: MorphoSys AG via EQS Newswire.
The Pharma Data
AUGUST 15, 2021
Food and Drug Administration (FDA) has granted Fast Track designation to VTX-801, Vivet’s clinical-stage gene therapy for the treatment of Wilson Disease – a rare, genetic disorder that reduces the ability of the liver and other tissues to regulate copper levels, causing severe hepatic damage, neurological symptoms, and potentially death.
Cloudbyz
AUGUST 15, 2024
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 clinical supply management?
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