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Get the latest updates, insights and best practices on data management and biostatistics in clinical trials.

Bioforum Expands Leadership Team with Appointment of Michael Goedde as President

Life Sciences Industry Veteran to Lead Development and Execution of Growth and Innovation Strategy, Expanding Global Reach of Bioforum’s Biometric Services and Solutions  Bioforum, the Data Masters, a leading contract research organization (CRO) focused on the delivery of biometric services and solutions to the global clinical trials industry, today announced the appointment of Michael Goedde …

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Bioforum Signs Exclusive Deal to Acquire Assets from Abond CRO Inc., Expanding Reach of Global Biometric Services

  Abond Selects Bioforum to Deliver Continuity of Statistical Analysis and Data Management Support Services to Clinical Trial Sponsor Clients Worldwide   US-Based Biotechs Transition from Abond to Bioforum to Drive Clinical Trial Efficiency and Optimization       Bioforum, the Data Masters, a leading contract research organization (CRO) focused on the delivery of biometric services and solutions …

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FREE WEBINAR: Accelerating Submissions: Understanding FDA’s NDA Data Submission Requirements and Developing Biometrics-focused Strategies to Reduce Costs and Save Time

  Click to Watch the Recording Date: Tuesday, February 6, 2024 Time: 10:00 a.m. · Seoul (GMT +9:00) Webinar description: Join Amanda Cross, Bioforum’s Chief Operating Officer, to learn how a data-first approach to outsourcing can speed your FDA submission timelines. Agenda: An overview of the Integrated Summary of Efficacy (ISE) and Integrated Summary of …

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Adapting Computer System Validation (CSV) to Evolving Technological Landscapes: A Strategic Modernization Approach

Click to Watch the Recording Join Limor Teomim and Ido Raz as they look at a strategic modernization approach to adapting computer system validation (CSV) to evolving technological landscapes define risks in software validation: How technology changes impact software risk management How to implement risk-based approach in SaaS Regain system ownership with modern software validation …

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Bioforum Expands Clinical Trial Technology and Services with Acquisition of Validify

Acquisition Adds Computer Systems Validation Automation Capabilities, Further Enriching Bioforum’s End-to-End Suite of Solutions for Clinical Trial Data Management NESS ZIONA, Israel, Nov. 20, 2023 /PRNewswire/ — Bioforum, a data-focused, technology-driven CRO, today announced the acquisition of Validify (Applato Systems Ltd.), a leader in the automation of computer systems validation (CSV). With this expansion, Bioforum is addressing the growing demand for …

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Bioforum has been shortlisted for Citeline’s 2023 Scrip Awards!

Exciting news! Bioforum has been shortlisted for Citeline’s 2023 Scrip Awards in the “Best Contract Research Organization – Specialist Providers” category! It’s an honor to be recognized for the work we do to help clinical trial sponsors improve and innovate data processes. We’re proud of our long-term, trusted partnerships with clients around the world and …

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CROs Leading The Way In Modern-Day Clinical Data Management

By Deborah Borfitz  July 13, 2023 | Contract research organizations (CROs) increasingly find themselves on the leading edge of changes afoot in clinical data management, making it less about the policing of information and more about extracting meaningful insights from it. Among them are global CRO Bioforum, which specializes in creating efficiencies through data linkages and …

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Celebrating Bioforum and Medidata’s 10 Year Partner Anniversary

  “For over a decade, we have helped clinical trial sponsors drive innovation on the Medidata Clinical Cloud. As a boutique CRO specialized in data management, biostatistics and medical writing, with clients all over the world, Bioforum is focused on delivering high-quality data and leveraging technology that enables sponsors to build the agility, scale, and …

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FREE WEBINAR: How to Get the Best From Your Medical Writing Vendor: An Open Conversation with Angela Burnett and Shiri Diskin

  Click to Watch the Recording Medical Writing department heads from Bioforum and RRD International will discuss how to effectively select medical writing vendors and manage medical writing outsourcing. With over 30 years of experience leading regulatory medical writing groups in the drug/biologic development industry, this will be a frank exchange of ideas and practical …

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FREE WEBINAR: SDTM Data Completeness & Audit Trail Webinar

Click to Watch the Recording Join Tanya du Plessis and Eyal Wultz as they take a look at an innovative approach to solving two of the major challenges facing SDTM: • How can you ensure all your clinical data ends up in SDTM? • How can you show an audit trail of your SDTM data …

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