Systech provides digital identification and traceability solutions that establish essential product data, ensure digital connectivity and enable real-time insights on the packaging line and throughout the supply chain. With decades of experience in pharmaceutical packaging execution and serialization, Systech offers comprehensive, easily configured, turnkey software solutions with reliable implementation and expert support. Global brands across industries rely on Systech’s platform to help them achieve their objectives in compliance, brand protection, resiliency and digital transformation. Systech is a leading brand of Markem-Imaje®, a global product identification, packaging intelligence and connected product solutions provider.

Honeybee Trials is a clinical trial patient recruitment platform. Historically, 90% of clinical trials are delayed and 30% are terminated due to challenges with patient enrolment. The disparity in clinical data is jarring, as 99.99% of the global population is under-represented in the research that drives health advancements in our communities. At Honeybee, we believe that the solution starts with giving clinical teams the toolset to improve the patient's clinical trial journey. We're building data-driven software to change the way patients discover, enrol, onboard and participate in clinical trials. We're driving higher participation rates, greater diversity and lower attrition in trials to bring health products & services to market faster than ever before.

Consilx is an award winning technology platform provider for decentralized clinical trials. ConsilX is founded by senior executives with extensive experience in clinical drug development, service industries and academic research institutions. Our clients include Top-10 Pharma, Global CRO Consortium, mid-tier CROs, and Research organizations. The digital platforms provided Consilx are: a) Digital Consenting platform for site-based & remote consenting. We also have an eConsent-Lite. b) Patient Engagement solutions including visits tracking, medications compliance, adverse event alerts, etc. c) Direct Data Capture through eSource (for site-based & tele-visits), eDiaries, questionnaires, wearables, devices d) Telemedicine - Online video and audio communication between site and patients and related workflows e) LifeLedger™ - Decentralized trial platform managing the entire conduct of a clinical trial f) Blockchain-based Micro Platforms for data notarization, post-trial data access to patients for permissioned sharing, verified & automated data and documents exchange amongst clinical trial partners Visit us at www.consilx.com or write to us at info@consilx.com for more information.

VCTC is a new type of clinical research site, specialised in making clinical research accessible and meaningful for anyone, anywhere. Our innovative approach is proven to accelerate and enhance research outcomes, enabling better clinical decision-making and facilitating the faster introduction of new and improved medical treatments. Participants are always at the centre of everything we do and we pride ourselves on offering an exceptional, safe and inclusive experience for everyone involved. We consistently achieve faster and more diverse recruitment of participants compared with other models. At the heart of our team are medical, scientific and clinical specialists, meaning that trial participants - and our clients - have ready access to the expertise, support and help they need throughout. This consistently results in enhanced research evidence and high participant retention rates. We provide support for all components of clinical research, from leading a trial end-to-end, to advising on best practice or developing accessible trial guidance and other materials. We aim to push boundaries and continually improve the quality of clinical research, leading a lasting, meaningful transformation in the way clinical research is conducted worldwide.

A scalable and industry wide recognized clinical trials database registry created to improve clinical trial participant safety and data quality by preventing duplicate enrollment and key protocol violations. Verified Clinical Trials is a global organization used across multiple therapeutic indications and all phases of clinical trials research.

Clinical Ink, Inc. provides eSource solutions for the clinical trials industry. It offers SureSource, an electronic source solution that allows users to record comments, explanations, and validated source data on protocol-specific eSource documents, as well as captures the data required by the protocol. The company also provides an electronic source record (ESR) for clinical trials that provides cleaner data. In addition, it offers hosting services. Clinical Ink was founded in 2006 and is based in Winston-Salem, North Carolina.

FiCRO offers tailored solutions for both preclinical and clinical trials to bio-ventures. We are dedicated to mediating between bio-ventures and CROs, ensuring efficient trial operations by collecting and maintaining up-to-date data. Numerous bio-ventures worldwide rely on Contract Research Organizations (CROs) to prepare for clinical trials. By offering a service that matches sponsors' RFPs with the most optimized CROs based on data, MEDIAIPLUS aims to reduce both the time and cost required for bio-ventures to conduct clinical trials.

IgniteData’s Archer technology is transforming the way hospitals and research sites transfer data for clinical trials. EHR-to-EDC data transfer provides fast, accurate patient data for clinical studies, significantly reducing the requirement for laborious data transcription and source data verification (SDV).

GE Healthcare is a healthcare company with intelligent devices, data analytics, applications, and services-supported intelligence platforms. Their company operates at the center of an ecosystem working toward precision health, digitizing healthcare, helping drive productivity, and improve outcomes for patients, providers, health systems, and researchers around the world.

M&B Sciences, Inc, is a minority owned, tech focused life science research firm that is an industry leader in recruiting patients for global clinical trials, market research and pharmacovigilance studies. With a patient registry of more than 250,000 willing study participants across 308 different medical conditions, including rare diseases, we have completed more than 100 interventional and non-interventional global patient recruitment campaigns on behalf of our biotech, pharma, and healthcare clients.

Putting patients first is in uMotif’s DNA. The modern uMotif eCOA platform delivers faster, high-quality clinical trials and real-world studies by putting patients at the core of research. Combined with uMotif’s robust site tools – including consent management, site productivity, and trial awareness – the platform strengthens the patient-site relationship, which is key to improving eCOA compliance and retention. With cloud hosting in the US, Europe, and China, the GCP, 21 CFR Part 11 and GDPR-compliant platform supports all study phases and indications. Visit www.umotif.com

OpenDBM is an open-source platform that democratizes access to AiCure’s scientifically validated digital biomarker algorithms so researchers can apply them to their own datasets. This transparency encourages industry and academic collaboration, helping to validate digital biomarkers as a legitimate means to understanding disease and patient behavior.

Our Mission: Shaping a new clinical trial industry standard for data integrity that ensures trust, delivers value and elevates patient care! In the clinical trial ecosystem, reliable data is essential for a wide range of stakeholders: Regulatory Authorities, Key Opinion Leaders, Investors, Customers, Insurers, M&A Firms, and most importantly, patients. Blockchain technology is revolutionizing how clinical data is captured and stored. By design, it offers an unparalleled level of security compared to traditional systems and ensures a tamper-proof audit trail for clinical data, enhancing trust and transparency at every stage. With this robust foundation, you can confidently engage with your stakeholders, knowing that your data meets the highest standards of security, integrity, and reliability. Trust your data—and let it empower your success. Our passionate team members combine their expertise in a unique way. We are bringing together profound know-how in blockchain, information technology, pharma, medtech and clinical research thus briding the gap between business and technology.

Clinvigilant Research is a leading provider of comprehensive services to the life sciences industry, specializing in Contract Research Organization (CRO) services, eClinical solutions, and clinical consulting. Our mission is to empower pharmaceutical, nutraceutical, consumer, biotechnology, and medical device companies to bring innovative therapies to market efficiently, while maintaining the highest standards of quality and compliance. CRO Services As a full-service CRO, Clinvigilant Research manages clinical trials from start to finish. Our services cover: • Study Design & Protocol Development • Phase I - IV, RWE, PMS, and Observation Clinical Trials • Regulatory Affairs • Site Selection and Management • Clinical Monitoring • Data Management and Statistical Analysis We ensure that clinical studies are conducted according to Good Clinical Practice (GCP) and are compliant with global regulatory requirements. eClinical Solutions Our state-of-the-art eClinical solutions offer an integrated digital platform for managing clinical trials, streamlining processes, and improving data accuracy. Our solutions include: • Electronic Data Capture (EDC) • Clinical Trial Management Systems (CTMS) • Electronic Patient-Reported Outcomes (ePRO) • Risk-Based Monitoring (RBM) • Electronic Consent (eConsent) • Electronic Source (eSource) • RTSM These tools ensure that clinical trials run efficiently while providing real-time access to high-quality data. Clinical Consulting We offer tailored clinical consulting services to address the unique needs of our clients. Our experienced consultants provide expertise in areas such as: • Regulatory Strategy and Submissions • Study Feasibility and Optimization • Quality Assurance Audits • Market Access and Commercialization Clinvigilant Research is committed to being a trusted partner in advancing healthcare innovations by providing flexible, client-focused solutions that meet the challenges of clinical development.

We use new technologies combined with deep experience in supply chain processes to create easy to implement and cost-efficient applications. Our leading-edge sensors create digital tweens of the objects and allow them to stay connected with us, among them, and exchange in intelligent clouds. We provide near real-time Supply Chain transparency allowing the monitoring and management of exceptions. We provide tracing, avoid counterfeiting, damages (due to temperature, humidity or shock) and losses in supply chains, theft , waste in production and logistic asset utilization, and Billions in losses due to lack of transparency and lack of real-time monitoring of supply chains. Our solutions are based on multifunctional sensors (various measuring functions can be de-activated as required), are easy to install (plug and play), can be used without additional infrastructure, and with low maintenance ( years battery life). We also offer complete solutions, from sensors and cloud applications to transparency (real-time reporting), ad-hoc control (push information on emails, mobile phones, apps and other systems) and automated processing.

Now part of Clinical Ink, the life sciences technology company that brings data, technology, and patient science together. Our deep therapeutic-area expertise, coupled with eSource, Direct Data Capture, eCOA, eConsent, telehealth, and digital biomarker advancements, drive the industry standard for transparency and precision. Our solutions power sponsors, CROs, researchers, and patients to recenter decentralized trials and rewrite clinical discovery.

Elligo Health Research is an integrated research organization founded to bridge the gap between cutting-edge clinical trials and the patients who need them—an idea that sparked when our founder's barber couldn't access a promising treatment. By embedding research into routine care, Elligo empowers physicians to offer trials to their own patients, expanding access, improving diversity, and reducing barriers through additional travel and retention support services. Sponsors and CROs benefit from a nationwide network of research-ready sites—traditional and decentralized— backed by EHR data integration and proven recruitment strategies. With flexible service models, Elligo supports each site’s unique needs, from infrastructure and staffing to full-service trial operations. Our mission is to accelerate clinical research and bring life-changing therapies to more people, faster.

TraceLink is the only network creation platform company that builds integrated business ecosystems with multienterprise applications - the true foundation for digitalization - delivering customer-centric agility and resiliency for end-to-end supply networks and leveraging the collective intelligence of entire industries. Delivering end-to-end supply chain solutions, TraceLink's Opus Platform enables speed of innovation and implementation with an open partner model for no-code and low-code development of solutions and applications. At TraceLink, we blend decades of knowledge in SaaS technology and supply chain business processes with a clear vision for advancing manufacturing industries through disruptive, unconventional software solutions. With headquarters in Massachusetts, TraceLink has six global offices through North America, South America, Europe, and Asia.

RM2 launched the smart reusable pallet revolution by embedding autonomous IoT sensor technology in its logistically optimized, hygienic BLOCKPal™ reusable composite pallets. IoT sensor data are transmitted to the cloud via the LTE-M network, making visible the pallet’s location and condition both indoors and in transit without requiring any additional hardware or IT development or training. RM2’s End-to-end Logistics Intelligence Optimization and Tracking (RM2 ELIoT®) technology - the Company’s cloud-based supply chain intelligence platform - captures and contextualizes location, temperature, shock, and event data, giving customers end-to-end supply chain visibility and clear, actionable insights in real time. RM2 issues, retrieves, and sanitizes more than 1.5 million reusable IoT pallets annually through a nationwide network of over 30 service facilities in a cost-effective, scalable, and environmentally sustainable pallet pooling system. Learn more at www.RM2.com.

SCMIND is a leading supply chain & management consultancy specializing in the pharmaceutical supply chain, Global Track & Trace, and Digital Transformation.

IVR Clinical Concepts is a specialty company devoted to developing and implementing cost-effective, secure Interactive Voice and Interactive Web Response applications (IVR/IWR, a.k.a. IxRS and IRT) that interface seamlessly with other technologies and provide data collection and reporting tools that enhance comprehensive management of clinical studies. Users, sites and subjects, can enter data using either IVR or IWR in the same application, per their needs or preferences; all data entered then integrate directly to EDC systems for virtually immediate real-time data, real-time reports and real-time results for pharmaceuticals, biotechnology and medical device trials. IWR applications can be designed to work on Microsoft Windows, Apple and Android devices according to the needs of the study. Clients who choose IVR Clinical Concepts for their IVR/IWR solutions are rewarded with flexible data input in globally available applications that put key decision-making information at their fingertips.

Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our 24,000+ professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™ We continue to earn recognition industrywide, including the 2025 Scrip Award for “Best Contract Research Organization – Full-Service Provider,” 2024 Fierce Biotech CRO Award for "Innovative Approaches to Patient-Centric Research" and the 2024 and 2023 Society for Clinical Research Sites (SCRS) Eagle Award. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove comments that do not adhere to our guidelines and report users who violate the rules of our page.

Hawthorne Effect's mission is to make clinical trials accessible to everyone, everywhere. The company's proactive Visit Management System honors the relationship between sponsors and their investigators and promotes the use of shared technology to ensure protocol compliance and eliminate missing data. By enabling research teams to not only track all of their patients and thousands of data points but deploy specially trained healthcare providers (“HEROs”) to conduct visits anywhere, anytime, Hawthorne Effect ensures that no patients are “lost to follow-up.

Clinical and Consumer Insights Anywhere, Anytime.

A niche consultancy with over twenty years of both Clinical Data Management and Database Services expertise. We partner with pharmaceutical, biotech and medical device companies to ensure they have the support and expertise in-house to successfully execute their trial from the data management perspective.