• ‘Professional Patient’ Detection Now A Clinical Study Essential

    Apr 13, 2022, 01:00 by User Not Found
    Clinical Research News | After more than a decade in the business of detecting “professional patients,” Verified Clinical Trials is a familiar name to stakeholders across the research enterprise—including the nefarious players who ride-share from city to city in search of unprotected sites where they can enroll in studies purely for the financial gain. It’s an underappreciated underground economy that is costing sponsor companies time and money and, in some cases, completely shutting down studies, according to Mitchell Efros, M.D. FACS, CEO of Verified Clinical Trials.
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  • Seqster Launches Real World Data Tools on Salesforce AppExchange

    Apr 12, 2022, 16:21 by User Not Found
    Clinical Research News | Seqster PDM has launched SeqsterOS, the operating system for patient registries and clinical studies on Salesforce AppExchange integrated directly with Salesforce Health Cloud. SeqsterOS seeks to empower life science enterprises to seamlessly integrate patient-consented Real World Data, including electronic health records (EHR), genomics, and device data, with a patient engagement layer for their clinical studies.
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  • EMA Endorses Biomarkers For Type 1 Diabetes Prevention Trials

    Apr 11, 2022, 01:00 by User Not Found
    Clinical Research News | Following many years of collaborative patient-level data sharing across stakeholder groups, the European Medicines Agency (EMA) recently endorsed pancreatic islet autoantibodies as enrichment biomarkers for type 1 diabetes (T1D) trials focused on delaying or preventing the disease. The Qualification Opinion appears on both the EMA website and that of the Critical Path Institute’s (C-Path) Type 1 Diabetes Consortium (T1DC).
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  • Building Clinical Trial Infrastructure for Greater Diversity

    Apr 8, 2022, 01:00 by User Not Found
    Clinical Research News | The life sciences industry has faced recent criticism for its continued challenge to boost diversity in clinical trials. Reports suggest that the US Food and Drug Administration (FDA) is currently at work on guidance that will define how the agency would interpret “adequate representation” of ethnic, racial and age diversity to increase representation of traditionally underrepresented populations in drug development. This will ensure organizations are broadening eligibility criteria through inclusive trial practices and trial design.
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  • DFE Pharma, Harro Höfliger, and Sterling partner in “INTO” to provide formulation services for respiratory products

    Apr 7, 2022, 18:05 by
    DFE Pharma, Harro Höfliger, and Sterling partner in “INTO” to provide formulation services for respiratory products Inhalation Together (INTO) helps pharmaceutical companies in the respiratory field to simplify formulation development New York, USA (24th March 2022) – Three leading companies in their respective fields - DFE Pharma (excipients solution provider), Harro Höfliger (equipment supplier), and Sterling (API manufacturer) - announced a unique partnership with the establishment of “Inhalation Together” (INTO) in the field of dry powder inhalation (DPI).
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  • BOC Sciences Optimizes PROTAC Platform to Boost Related Research

    Apr 7, 2022, 18:05 by
    BOC Sciences optimizes its PROTAC platform of protein degradation technology to boost PROTAC research and development.
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  • Creative Bioarray Develops Cell Immortalization Kits and Immortalized Human Cells to Support Immortalized Cell Research

    Apr 7, 2022, 18:05 by
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  • ActiGraph Joins Decentralized Trials & Research Alliance

    Apr 7, 2022, 18:05 by
    ActiGraph further solidifies its reputation as an innovator in clinical trials by joining an organization aimed to make research participation accessible to all.
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  • CD Formulation Announces to Offer Nitrosamine Impurities Analysis Service for Drug Formulation Projects

    Apr 7, 2022, 18:05 by
    Earlier this month, CD Formulation announces that it is now capable of providing nitrosamine impurities analysis service for customers who are involved with drug formulation projects and need help from CRO companies like CD Formulation.
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  • Tower Cold Chain launches KTEvolution container for pharmaceutical transport

    Apr 7, 2022, 18:05 by
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  • Stanley Capital-backed portfolio company DSS acquires MyMeds&Me

    Apr 7, 2022, 18:05 by
    Stanley Capital-backed portfolio company DSS acquires MyMeds&Me 04 April 2022, London - Stanley Capital Partners LLP (SCP), the European and US-focused mid-market private equity firm, today announced the acquisition of MyMeds&Me Limited (MMM) by its portfolio company Drug Safety and Pharmacovigilance Services Solutions (DSS). DSS is a leading global provider of pharmacovigilance services under the brand Bioclinica. The financial terms of the transaction are not being disclosed.
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  • BioIVT Acquires Commercial Blood Bank Tennessee Blood Services

    Apr 7, 2022, 18:05 by
    This transaction expands BioIVT’s donor network and increases its capacity to provide fresh whole blood, plasma, serum, and red blood cells for drug and diagnostic development.
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  • CPHI North America opens as 65% of US companies forecast growth in excess of 20% in 2022

    Apr 7, 2022, 18:05 by
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  • Valo Health Acquires TARA Biosystems Creating First of its Kind Vertically Integrated Cardiovascular Platform

    Apr 7, 2022, 18:05 by
    Valo Health Acquires TARA Biosystems Creating First of its Kind Vertically Integrated Cardiovascular Platform
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  • CluePoints Continues Impressive Global Growth with Three New Senior Appointments

    Apr 7, 2022, 18:05 by
    CluePoints Continues Impressive Global Growth with Three New Senior Appointments The company welcomes new VP Marketing, VP People, and VP Business Operations to its expanding team King of Prussia, PA – 5th April, 2022: CluePoints, the premier provider of Risk-Based Study Execution (RBx) and Risk-Based Quality Management Software for clinical trials, has appointed Catherine Ditzler as VP Marketing while Céline Daubresse joins as VP People, and James Faust is the new VP Business Operations.
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  • ArisGlobal Expands LifeSphere Clinical Portfolio with Landmark Customer Wins in APAC & Middle East

    Apr 7, 2022, 18:05 by
    ArisGlobal, the leading provider of life sciences software that automates core drug development functions with its end-to-end technology platform LifeSphere®, today announces significant growth in the global footprint of its LifeSphere Clinical software, following the customer wins of two prominent institutions in the Asia Pacific and Middle East regions.
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  • Celerion Announces Investment in ADME Suite of Services

    Apr 7, 2022, 18:05 by
    Celerion, a clinical research organization (CRO) to the biopharmaceutical industry, has announced that it has made a significant investment in its ADME (Absorption, Distribution, Metabolism and Excretion) suite of services to meet continuously increasing demand to conduct these studies. This investment includes expanding laboratory space, adding new capabilities as well as a dedicated customer service team.
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  • Rho Hires Global VP of Quality Assurance to Support International Expansion following Acquisition

    Apr 7, 2022, 18:05 by
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  • Matching Japan’s Real-World Databases To Research Purposes

    Apr 7, 2022, 01:00 by User Not Found
    Clinical Research News | Japan has a variety of databases available to researchers, but knowledge and experience is needed to understand the characteristics of each one and select wisely, according to two representatives of CMIC Group, the country’s largest contract research organization. The database options are tied to Japan’s publicly funded healthcare system that provides universal health insurance and the freedom to choose among medical institutions offering consistently high-quality, low-cost medical care.
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  • The Scope of Things: Craig Lipset on Decentralized Trials, the New Risk Model, and Open Doors

    Apr 5, 2022, 10:05 by User Not Found
    Clinical Research News | The pandemic has certainly been a turning point for decentralized trials, and Craig Lipset, co-chair of the Decentralized Trials and Research Alliance (DTRA) says the reasons are clear: the industry’s understanding of risk.
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