2026 Sponsors & Exhibitors

Cytel is the largest provider of statistical software and advanced analytics for clinical trial design and execution. For over thirty years, Cytel’s scientific rigor and operational excellence have enabled biotech and pharmaceutical companies to navigate uncertainty, prove value and make confident, evidence- based decisions. Our experts deliver industry-leading software, data-driven analytics, real-world evidence and strategic consulting. Headquartered in Waltham, Massachusetts, Cytel has more than 1,400 employees across North America, Europe and Asia. For more information about Cytel, please visit www.cytel.com. 

Dr. Vince Clinical Research (DVCR) is a full-service contract research organization (CRO) specializing in early phase trials in both healthy normal volunteers and patient populations across a wide range of trial designs and therapeutic areas such as neuroscience, substance abuse, pain, cardiometabolic disorders, infectious diseases and many others. CRO services include project management, data management, biostatistics, statistical programming, PK/PD analysis, medical writing, monitoring as well as site feasibility and management for multi-site trials. Additionally, DVCR operates one of the most innovative and technologically advanced clinical pharmacology units in the world with over 90 beds for overnight confinement, a cGMP compliant pharmacy as well as luxurious amenities to support diverse study participant recruitment and retention. By leveraging technology and one of the country’s most experienced leadership teams in early clinical development, DVCR provides Smarter Faster Data® to their biopharmaceutical clients. For more information, please visit https://sponsors.drvince.com/

Harbor Clinical is a women-owned clinical research services firm. As a Functional Service Provider (FSP) offering Staff Augmentation, Consulting, and Single-Service resourcing models, Harbor Clinical’s mission is based on the goal of forging innovative partnerships, with sponsors and employees, built on a bedrock of communication and transparency. To learn more, please visit https://www.harborclinical.com/

One2Treat is dedicated to transforming the way biopharmaceutical companies design, analyze and interpret randomized clinical trials, and how the overall medical value of a treatment may be communicated. Through its innovative software platform and patient-centered methodologies, One2Treat helps sponsors incorporate the patient's voice into early trial design, endpoint selection, and treatment value assessment. By aligning clinical evidence generation with patients and clinicians’ needs, One2Treat supports more meaningful clinical trials, efficient decision making and enhanced regulatory discussions, leading to faster market access. For more information, please visit https://one2treat.com/

Scimega is a niche Canadian oncology CRO acting in Canada within the context of global cutting-edge oncology trials sponsored by U.S. mid-size and smaller biotechs. Skilled in collaborative vendor teaming, Scimega guarantees sponsors the quickest site start-up and highest patient recruitment rate, without sacrificing premium quality data.

With an optimal operations design robust enough to address an ever-changing clinical trial landscape, Scimega’s team of Lean Coached oncology experts go above-and-beyond to provide: Local, full-time, permanent hires for exceptional staff quality; An extensive network of Canadian Investigator Sites that frequently emerge among top enrollers, and are activated 50% faster than average for global studies; Optimal site engagement to maximize quality, timely data entry and query resolution; Robust and Lean Scimega methodology and processes are supported by current technology to keep every trial this CRO monitors on the Lean trajectory.

Learn more about the Canadian opportunity or explore an expansion with Scimega!

For more information, please visit:

www.scimega.com    https://scimega.com/blog/       info@scimega.com

The Weave Platform is an AI-native regulatory automation platform with built-in AI templates—AutoIND for INDs and AutoCT for clinical documents—designed to support regulatory dossiers across all stages of drug development, accelerating timelines, enhancing quality, and managing complexity. Learn more at www.weave.bio.

Worldwide Clinical Trials (Worldwide) is a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications, from discovery to reality. Our full-service clinical development capabilities include bioanalytical laboratory services and Phase I-IV clinical trials, as well as post-approval and real-world evidence studies – all powered by our talented and accessible team of clinicians, scientists, and researchers who bring their first-hand expertise to each clinical program.

At Worldwide, we understand that each customer and project are unique, so we take a collaborative and personalized approach to identify and meet specific needs and goals. Anchored in our company’s scientific heritage, we are therapeutically focused on cardiovascular, metabolic, neuroscience, oncology, and rare diseases. We apply this deep therapeutic knowledge to develop flexible plans and quickly solve problems in the rapidly evolving clinical development landscape.

Our team of 3,000+ professionals spans 60+ countries, and believes that through collaboration, and a culture that embraces diversity, equity, inclusion, and belonging (DEI&B), everyone plays an important role in making a world of difference for patients and their caregivers. We are united in cause with our customers to improve the lives of patients through new, innovative therapies.

For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

The PPD clinical research business of Thermo Fisher Scientific enable customers to accelerate innovation and increase drug development productivity. Utilizing patient-centered strategies and data analytics, our capabilities cover multiple therapeutic areas and include early development, all phases of clinical development, peri- and post-approval, novel approaches to patient recruitment and investigator sites, and comprehensive laboratory services. For more information, please visit https://www.thermofisher.com/ppd

Delve Health is an innovative biotechnology solutions company dedicated to revolutionizing the way clinical trials and healthcare organizations leverage data for improved patient outcomes and operational efficiency. By harnessing the power of wearables, biosensors and AI and leveraging the real-world data (RWD) collected by remotely monitoring patients, Delve Health delivers quality analytics to researchers and healthcare professionals. We provide actionable insights to make informed decisions, drive transformative outcomes and enhance patient care—all while removing social determinants of health (SDOH) barriers. For more information, go to https://delvehealth.com/

Barrington James are an industry leading, global recruitment business that exclusively serves the Pharmaceutical, Biotechnology and Medical Device sectors. With offices all over the world and hundreds of specialists dedicated to sourcing exceptional talent, we have the capacity and capabilities to deliver world-class recruitment solutions to Life Science companies of all sizes. To learn more, please visit https://barringtonjames.com/

BioPoint is a US-based life sciences consulting organization that brings decades of industry knowledge and expertise to our clients. We offer flexible support whether it is a need for a single resource or our specialized FSP approach, BioPoint can support all facets of drug development. To learn more, please visit https://biopointinc.com/.

At Faro, we're redefining how clinical trials are designed and executed. Our AI-powered platform streamlines protocol development and connects design decisions to downstream workflows, enabling faster, more efficient clinical studies. From first draft to final protocol, Faro reduces manual effort and simplifies collaboration across functions, accelerating study startup and ensuring operational alignment from day one. With structured clinical knowledge and dynamic orchestration, teams can identify risk earlier, improve consistency, and design patient-centered studies that scale. The result: fewer amendments, faster timelines, and more efficient trials built on a foundation of connected, intelligent processes. For more information, visit farohealth.com.

At Inizio Biotech, we understand that every day is an opportunity to build towards the true value of your assets. Providing best-in-class services across the clinical development and commercialization journey, our biotech solutions are highly personalized and coordinated through a single strategic point of contact. We support you by guiding, validating, and inspiring the decisions that matter most. To learn more, please visit https://inizio.health/

Lumanity is a global healthcare advisory firm committed to bringing human perspectives to the forefront, integrated with sound science and business strategy, to realize a bold vision of fearless innovation and drive more authentic human touchpoints from discovery to care. Our passionate, diverse specialist team of patient advocates, clinical, scientific, and subject matter experts embed humanity and insight into meaningful solutions, co-created with communities to illuminate the path to healthcare that matters to patients. We believe the path of innovation starts and ends with the human lived experience. Learn more at https://lumanity.com/patient-engagement/

Miracle accelerates clinical trials with real-time, automated insights across enrollment, patient profiles, safety, labs, data management, forecasting, and more. By aggregating and harmonizing siloed data, Miracle helps biopharma companies reduce delays, make faster decisions, and centralize communication. Customers have cut months off trial timelines by eliminating manual processes and inefficiencies. For more information, please visit https://www.miracleml.com/

For more information, please visit https://mmsholdings.com/ 

For more information, please visit https://www.perspectivepv.com/

PhaseV is a technology company leveraging advanced causal inference and machine learning to innovate clinical trials. Our technology and methods enable to optimize trial design by detecting hidden signals in existing clinical data and extracting actionable insights, as well as supporting advanced adaptive designs for more efficient, precise and successful clinical trials. For more information, go to www.phasevtrials.com

Phastar is a leading, award-winning, specialist Biometrics CRO that provides statistical consulting, analysis, reporting, data management and data science services to small and large biotechnology, pharmaceutical and medical device companies across the world. We leverage collaboration, technology, clinical data, and our worldwide presence to optimize decision-making for safety, quality, and efficiency. With 15 offices worldwide, our number one priority is ensuring on-time, quality work and assisting our customers in optimizing their clinical research. For more information, please visit https://phastar.com/

Precision for Medicine is the first global, precision-medicine, clinical research organization and a leader in complex clinical development. Our clients benefit from advanced technologies and new approaches that compress timelines, gain efficiencies and increase the probability of approval. Under one global roof, Precision has worldwide CRO services, integrated sophisticated biomarker capabilities, technical manufacturing solutions and more. With 7 specialty labs and 3500+ professionals worldwide, we help clients accelerate life-changing treatments and propel medicine forward. For more information, visit https://www.precisionformedicine.com/

At SSI Strategy, we're strategic partners deeply invested in our clients' success. We offer a unique, adaptive approach to supporting biotech companies, integrating business acumen with deep expertise in Clinical Development & Operations, Regulatory affairs, Pharmacovigilance, Medical Affairs, Quality and more.

Our agile skills and resources model allows us to adapt to your specific needs, working as an embedded team within your organization. We complement your existing teams, scaling specialized skill sets up and down as needed, while equipping them with the tools and resources to operate at peak performance. By fostering the organization you want to build, we position your full-time employees to be more successful and effective in their strengths. As your needs evolve, so does our support. We offer deep expertise, strategic insight, and a comprehensive range of services to help you navigate the challenges of bringing a therapeutic from concept to commercialization.

Our mission is clear: Build better biotechs through seamless collaboration, informed decision-making, and accelerated progress.

For more information, please visit www.ssistrategy.com

The Higgins Group, Inc. is an executive search and consulting firm focused exclusively in the life sciences. For over two decades we’ve been helping our clients thrive by going beyond recruiting the best leaders: as a strategic partner we consult on organizational issues that affect executive integration, retention, and performance. This approach has led to long-lasting relationships with a select roster of global pharmaceutical and biotech clients, helping us to grow exclusively through referrals since 1998. Today, we offer three practices to help our life sciences clients improve performance, retain talent, and accelerate ROI: Our Executive Search Practice specializes in finding physicians and R&D executives with the credentials, qualities, and cultural fit to drive superior company performance. Our Leadership Development Practice boosts performance with executive coaching and customized workshops to integrate new executives and create sustainable leadership improvements in individuals and teams. Our Board Impact Practice enhances board decision-making by recruiting and developing diverse, high-performing leaders who can help guide life sciences firms to realize their vision. All three practices are based on a simple, powerful premise: great leaders drive great performance. To learn more, please visit www.higgins-group.com

Founded in 2018, TruTechnologies is the leading provider of real-time clinical trial oversight, focused on enabling timely, high-quality data and mitigating risks in drug development. The company partners with six top 20 pharmaceutical companies and numerous biotechnology firms to accelerate patient screening and enrollment, drive protocol adherence, and correct deviations. For more information, please visit www.trutechnologies.io

Alpha Clinical is a boutique consulting firm specializing in clinical development, end-to-end pharmacovigilance services, regulatory affairs, and R&D consulting. We provide comprehensive solutions, including clinical operations, site management, medical affairs, and strategic due diligence, ensuring compliance with global standards while prioritizing patient safety. Our expertise drives excellence across the pharmaceutical and biotech industries. For more information, please visit https://alphaclinicaldevelopments.com/

Q2BI is a biometrical and clinical science contract research organization (CRO) for the life science industry product/drug development and regulatory submissions. Founded in 2009, Q2BI has a broad range of expertise-based services in the areas of Electronic Data Capture (EDC), Clinical Data Management (CDM), Medical Services (Medical Writing, Medical Monitoring, Medical Coding), Statistical Programming, Biostatistical science, Safety Monitoring including IDMC/DSMB, Pharmacokinetics / Pharmacodynamics (PK/PD), Data Science including data visualization/analytics and System Validation Consulting. Q2BI is a pioneer in adopting CDISC and supported the world’s first FDA Project ORBIS.

For more information, please visit https://sumptuous-ds.com/

Thorough Group delivers elite biotech human capital talent solutions, connecting innovative companies with top-tier leaders and specialists. With 85+ years of expertise across our leadership team, we align mission-driven professionals to fuel breakthroughs and accelerate growth. Our strategic, insight-driven approach ensures cultural and operational fit for long-term success. For more information, please visit WWW.Thoroughgroup.com