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Otto Damsma Joins Bioforum as Vice President of Asia Pacific Operations
Otto Damsma Joins Bioforum as Vice President of Asia Pacific Operations

We’re delighted to welcome Otto Damsma to Bioforum! Otto, who has more than 30 years of industry experience across biopharma, CRO and academic settings, joins our global team as Vice President of Operations for Asia Pacific to lead Bioforum’s continued growth and expansion in the region.   Otto Damsma Vice President of Operations for Asia …

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PharmaVOICE 100 Celebration: A Conversation with RedHill Biopharma, Alkermes, and PharmaVOICE: “Developing Clinical Trial Outsourcing Strategies that Scale As Biotechs Do”
PharmaVOICE 100 Celebration: A Conversation with RedHill Biopharma, Alkermes, and PharmaVOICE: “Developing Clinical Trial Outsourcing Strategies that Scale As Biotechs Do”

2020 has proven to be an incredibly pivotal time for the life sciences industry. While COVID-19 has created limitations around patient-doctor interactions and clinical trial operations, it has also demonstrated the opportunity that technology presents—and the power of fully embracing these tools to enable remote interaction and data transformation. Of course, challenges within the clinical …

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On-Demand Webinar Recording: “5 Key Considerations When Selecting an EDC Provider”
On-Demand Webinar Recording: “5 Key Considerations When Selecting an EDC Provider”

On-Demand Webinar Recording: “5 Key Considerations When Selecting an EDC Provider” As EDC in clinical trials becomes an industry standard, its benefits—no matter the software provider—seem universal: ease of use, remote access to information, mitigated risk around data entry and regulatory compliance, bountiful savings around time and cost, and so forth. But, with multiple vendors …

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We’re pleased to announce that our very own Irina Sher, VP of Data Management, has been recognized by the Healthcare Technology Report as one of the Top 25 Women Leaders in Biotechnology in 2020!
We’re pleased to announce that our very own Irina Sher, VP of Data Management, has been recognized by the Healthcare Technology Report as one of the Top 25 Women Leaders in Biotechnology in 2020!

The Healthcare Technology Report’s “2020 Top 25 Women Leaders in Biotechnology Award” We’re pleased to announce that our very own Irina Sher, VP of Data Management, has been recognized by The Healthcare Technology Report as one of the Top 25 Women Leaders in Biotechnology in 2020! Each year, the publication recognizes accomplished women who are …

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PharmaVoice June Issue: A New Era of Clinical Trials
PharmaVoice June Issue: A New Era of Clinical Trials

PharmaVoice June Issue: A New Era of Clinical Trials Bioforum’s Insights on how Industry Responds to the COVID-19 Pandemic Amir Malka, President & Co-Founder, BioForum the Data Masters Q: How have your business operations changed? Fundamentally, our business operations haven’t changed. They have been fortified with a renewed focus on value. Flexibility and being available …

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Veeva and Bioforum Partner with RedHill Biopharma to Maximize Value of Opaganib Phase 2/3 COVID-19 Clinical Data
Veeva and Bioforum Partner with RedHill Biopharma to Maximize Value of Opaganib Phase 2/3 COVID-19 Clinical Data

  Veeva and Bioforum Partner with RedHill Biopharma to Maximize Value of Opaganib Phase 2/3 COVID-19 Clinical Data Veeva Vault CDMS and Bioforum selected to optimize clinical data management for RedHill’s global Phase 2/3 clinical trial evaluating opaganib in patients with severe COVID-19 PLEASANTON, Calif. & NESS ZIONA, Israel–(BUSINESS WIRE)–Veeva Systems (NYSE: VEEV) (“Veeva”) and Bioforum today announced …

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COVID-19 Support plan for Emerging Biopharma
COVID-19 Support plan for Emerging Biopharma

COVID19 Support plan for Emerging Biopharma It’s is important to realise that every trial will (or already has been) impacted by the COVID19 pandemic. Even trials that are already running on a decentralised (or virtual) trial model are having to deal with the implications of missed visits or patients having to deal with COVID19. No …

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Interim User Guide - COVID-19
Interim User Guide – COVID-19

Interim User Guide – COVID-19 CDISC have released an Interim User Guide, freely available on their website, for studies pertaining to COVID-19. The User Guide provides examples and guidance on implementing CDISC standards for COVID-19 so that users can collect, structure and analyze data more effectively. The User Guide is part of a package that …

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Bioforum News - April 2020
Bioforum News – April 2020

Dear Colleagues and Friends, The ongoing spread of COVID-19 will continue to have major implications for clinical trial operations as we navigate through unchartered territory, and we’re committed to doing our part to support both the research community and the communities where we live and work. As more and more countries take action to manage …

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Coronavirus (COVID-19) Update: FDA Issues Guidance for Conducting Clinical Trials
Coronavirus (COVID-19) Update: FDA Issues Guidance for Conducting Clinical Trials

FDA NEWS  RELEASE Coronavirus (COVID-19) Update: FDA Issues Guidance for Conducting Clinical Trials For Immediate Release: March 18, 2020 The U.S. Food and Drug Administration today issued a guidance for industry, investigators and institutional review boards conducting clinical trials during the coronavirus (COVID-19) pandemic. The FDA recognizes that the COVID-19 pandemic may impact the conduct of clinical …

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Bioforum Partners with Mednet to Accelerate Clinical Development
Bioforum Partners with Mednet to Accelerate Clinical Development

Bioforum Partners with Mednet to Accelerate Clinical Development  Partnership Designed to Optimize Clinical Trial Efficiency and Flexibility MINNEAPOLIS and BOSTON – November 10, 2019 – Mednet, a provider of eClinical solutions for the global life sciences community and Bioforum, a global, data-focused contract research organization (CRO), announced a partnership designed to enhance the efficiency of …

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