Partners

Bioforum collaborates with leading service providers with proven clinical trials experience, products and services that our clients can count on to help them succeed.

Medidata is leading the digital transformation of life sciences, creating hope for millions of patients. Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users across 1,900+ customers and partners access the world’s most trusted platform for clinical development, commercial, and real-world data. Medidata, a Dassault Systèmes company, is headquartered in New York City and has offices around the world to meet the needs of its customers.

Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves.

Viedoc designs engaging software for the life science industry. By accelerating clinical trials on all levels, Viedoc’s solutions support major pharmaceutical, biotech, and medical device companies, as well as renowned research institutions worldwide. Headquartered in Uppsala, Sweden, Viedoc also has offices in America, France, Japan, Vietnam, and China. Since Viedoc’s inception in 2003, over 1 million patients in more than 75 countries have participated in studies powered by Viedoc

Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s flexible, electronic data capture (EDC)-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond simply EDC, Mednet’s comprehensive solution set provides the tools required to build and manage all types of clinical research, while adapting to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success.

At Medrio, we believe that clinical trial technology shouldn’t be difficult to use. That’s why our full-service eClinical Data Management suite helps streamline and decentralize your research and unify your solutions so you have more time to focus on your patients, rather than multiple vendors. Since 2005, our flexible technology has evolved alongside our customers to include an integrated suite of EDC, DDC, eConsent, RTSM, and ePRO/eCOA solutions that support your teams and sites, while reducing patient burden.

Let our solutions put you back in the driver’s seat with adaptive technology that easily powers mid-study changes and accelerates your trials, without compromising data quality. Or lean on our global team of experts who are available 24/7 to support you where you need it most. We’ve worked alongside Sponsors, CROs, and sites—spanning all therapeutic areas and trial phases—to secure over 770 approvals because we know it takes a village to achieve a healthier world.

uMotif’s mission is to put patients at the centre of clinical research. Designed with patients for patients, the uMotif patient-centric eClinical platform powers site-based to fully decentralised clinical, real-world, and post-marketing research. By engaging patients and healthcare professionals, uMotif is trusted by global pharmaceutical companies, biotechs, CROs, and academic institutions to capture eConsent and large volumes of ePRO, symptom, and wearable device data.

4G Clinical is a global leader in randomization and trial supply management (RTSM) for the life sciences industry, offering the only fully cloud-based, 100% configurable, and flexible solution utilizing natural language processing to accelerate clinical trials. 4G Clinical is headquartered in the U.S., within the Boston Biotech corridor of Wellesley, Massachusetts, and a West Coast office in Portland, Oregon. The company also maintains eight additional locations worldwide, with offices in Tokyo, Amsterdam, Dublin, Brussels, Tel Aviv, Basel, Nottingham, and Rheinbach.

Founded in 2000, MWB Consulting is now a premier boutique pharmaceutical consulting firm focused on the development and support activities in the pharmaceutical and medical device industries. MWB’s clients range from large pharmaceutical companies to small biotech companies in Europe, North America and Latin America.

MWB currently provides QPPV and pharmacovigilance consulting services and assist clients in resolving difficult product safety issues at the regulatory level.

We value our partners and are always looking to connect with like-minded, passionate & professional entrepreneurs. We’d love to talk to you about some of the ways we can work together.

Established in 1994, the Society for Clinical Data Management (SCDM) is a non-profit, international organization of over 2,800 members founded to advance the discipline of clinical data management.

SCDM members are charged with promoting quality and excellence in data management and are dedicated to the development, support and advancement of clinical data management professionals. SCDM is organized exclusively for educational purposes and seeks to engage with relevant organizations that can support to advance
its mission.

CDISC creates clarity in clinical research by convening a global community to develop and advance data standards of the highest quality. Required by the United States Food and Drug Administration (FDA) and Japan’s Pharmaceuticals and Medical Devices Agency (PMDA), recommended by the China National Medical Products Administration (NMPA) and adopted by the world’s leading research organizations, CDISC standards enable the accessibility, interoperability, and reusability of data. With the help of CDISC standards, the entire research community can maximize the value of data for more efficient and meaningful research that has invaluable impact on global health. CDISC is a 501(c)(3) global nonprofit charitable organization with administrative offices in Austin, Texas, with hundreds of employees, volunteers, and member organizations around the world.

ACDM represents enthusiastic clinical research professionals with a passion to improve the drug development process by offering an environment for continuous learning and application of contemporary Clinical Data Management practices.

Serving the data management community for over 30 years, our commitment is to provide explicit settings for our fellow members to network, share experiences & keep up to date with the latest regulations & standards in the area of Data Management. We also take pride in helping our members in their professional development journey. Our mission is to provide opportunities to constructively engage, collaborate and learn from the industry experts in Data Management, to equip members with the necessary skills to excel in their careers, so they can become the data management experts of the future.

EMWA is the European Medical Writers Association. EMWA is the network of professionals that represents, supports and trains medical communicators in Europe. It is a not-for-profit organization that is run for its members by its members. The European Medical Writers Association was founded in 1989 by a small group of professional biomedical communicators with academic, industrial and journalistic affiliations. EMWA has grown since then and now has over 1,000 members from 39 different countries (including 12 countries outside Europe), and includes academics and professionals working in-house or freelance for pharmaceutical and medical communications companies, research institutes, and in the field of scientific journalism.

AusBiotech is Australia’s biotechnology organisation, working on behalf of members for more than 35 years to provide representation and services to promote the global growth of Australian biotechnology. AusBiotech is a well-connected network of over 3,000 members in the life sciences, including therapeutics, medical technology (devices and diagnostics), food technology and agricultural sectors.

The BioMelbourne Network is a not-for-profit membership association for organizations engaged in biotechnology, medical technology and health innovation in the city of Melbourne in the state of Victoria.
The BioMelbourne Network’s role is to foster links between companies, research organizations, financial markets and government, creating a connected environment for greater collaboration and prosperity. The network’s mission is to build the ecosystem of capabilities in Melbourne to support the development and commercialization of new drugs, devices, diagnostics and digital health technologies to impact healthcare globally.

Via the Applied Knowledge Center, Bioforum provides educational courses and seminars to qualify the biomedical community and elevate its professional abilities. Our international faculty of more than 400 experts comprise academic scholars from applied and scientific disciplines, as well as professionals with profound industry experience.

In addition to furthering professional development for thousands of industry executives annually, Bioforum’s Applied Knowledge Center provides secretariat services for professional associations such as the Analytical Chemistry Association, the Israeli chapter of the PDA, the Industry Network of Advanced Cell Applications (INACA) and CannAlliance, among other organizations.

IMP offers comprehensive clinical supply management services in a controlled, monitored, licensed and certified GMP facility by the Israeli Ministry of Health.

IMP’s professional team accompanies each customer from study set-up to study completion and handles all study types; open-label or blinded studies, all phases (I-IV) and scales, including large-scale products and supply (for phase III studies) and complicated packaging campaigns.

IMP services include importation, sourcing, packaging, QP release, storage, distribution and more.
IMP works under the strict current GMP and GDP regulations to ensure safe, high-quality and cost-effective product and holds the Manufacturer’s/Importer’s Authorization with in-house experienced QPs for the certification/re-certification of clinical supply.