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Get the latest updates, insights and best practices on data management and biostatistics in clinical trials.
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Webinar: Best Practices For Executing EDC Protocol Amendments
Webinar: Best Practices For Executing EDC Protocol Amendments

Listen in to our recent webinar with Veeva Systems as Bioforum’s VP of Data Strategies and Solutions, Tanya de Plessis, joins Veeva’s Vice President, Vault CDMS, Richard Young, to discuss the best practices for executing EDC Protocol Amendments. If you couldn’t make it to the webinar or would like to rewatch it, visit the link …

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Bioforum has received ISO 27001:2013 certification for Information Security Management System (ISMS)
Bioforum has received ISO 27001:2013 certification for Information Security Management System (ISMS)

From Bioforum’s inception, we have demonstrated our commitment to quality and upholding the highest standards of information security to protect clinical trial data and assure its confidentiality, integrity, and availability. The ISO 27001:2013 certification is yet another external validation of our dedication to improvement in this area as we continuously review and strengthen our policies, systems, processes and culture to be best in class.

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Dr. Shiri Diskin, VP of Medical Writing, joins PharmaVOICE's editor-in-chief Taren Grom for an episode of the WoW (Woman of the Week) podcast series
Dr. Shiri Diskin, VP of Medical Writing, joins PharmaVOICE’s editor-in-chief Taren Grom for an episode of the WoW (Woman of the Week) podcast series

  Our very own Dr. Shiri Diskin, Bioforum the Data Masters’ VP, Head of Medical Writing, joins PharmaVOICE editor-in-chief Taren Grom for an episode of the WoW (Woman of the Week) podcast series. They chat about the critical role medical writers play in the drug development process, particularly drafting key regulatory documents and scientific journal articles, as well as Shiri’s passion for …

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Paul Malan Joins Bioforum as Vice President of Biostatistics
Paul Malan Joins Bioforum as Vice President of Biostatistics

We’re delighted to welcome Paul Malan to Bioforum! Paul brings 17 years of experience in planning and executing clinical trials, study designs, statistical analysis and reporting. He joins Bioforum from IQVIA, where he began his career as a statistician in 2003. Over the years, Paul held roles of increasing responsibility at IQVIA, moving up the …

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Webinar: Validation Strategies for Cloud-Based EDCs - More Innovation, Less Effort
Webinar: Validation Strategies for Cloud-Based EDCs – More Innovation, Less Effort

Validation concerns can hold companies back from adopting innovations in their clinical systems Validation concerns can hold companies back from adopting the latest innovations in their EDC systems. Differing opinions on the appropriate level of system validation can also add stress within an organization. It is possible to implement new features and stay validated with …

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Webinar: Applying the Principles of RBQM to Data Management
Webinar: Applying the Principles of RBQM to Data Management

Tanya du Plessis, our VP of Data Strategies & Solutions, and CluePoints‘ Rich Davies were discusssing RBQM. Watch the informative discussion on risk-based approaches to clinical data management and how to increase ROI, highlighting the latest industry trends, best practices and the most effective technology tools. Watch the recording>> Tanya du Plessis Vice President of …

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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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