27^th Clinical Trials
Innovation Programme

CLINICAL TRIAL SUPPLY MANAGEMENT: managing your Clinical Trial Material with agility. CREAPHARM is your experienced global partner for CTSM, specialized in clinical packaging, labeling and clinical logistics. Benefit from a worldwide scope with local specialists to maximize the success of your clinical trials!

CREAPHARM support you and your clinical trial with expert services in:

• Sourcing
• Highly-secured storage from -196°C to ambient.
• Clinical packaging/labeling of IMPs/IPs & blinding.
• EU QP-Release.
• Worldwide clinical logistics & cold chain management: adapted logistics with temperature-controlled transport solutions. Including ATMP Supply Chain management.
• Biospecimen Kit Assembly & Clinical samples logistics.

Florence is a trailblazer in Site Enablement solutions that redefine the landscape of clinical research operations. At Florence, our mission is clear: to streamline collaboration among research sites, sponsors, and CROs, ultimately closing the cure acceleration gap and revolutionizing the clinical trial industry. With the trust of more than 18,000 research teams across 55 countries, Florence prioritizes security and compliance, offering robust features, industry certifications, and seamless integrations for efficient trial management and has become synonymous with speeding up research, ensuring inspection readiness, and maximizing study capacity. Join Florence in shaping the future of clinical trials–where innovation meets collaboration, and breakthroughs become reality. To learn more about our Site Enablement solutions, visit www.florencehc.com.

Intertek has over 30 years of experience conducting regulated bioanalytical studies supporting and accelerating the development of pharmaceuticals, biopharmaceuticals, vaccines, and biosimilars. At our 30,000 square foot, state-of-the-art, GXP (GLP, GCP & GMP) European Centre of Excellence lab located in Manchester, UK, we provide global bioanalysis outsourcing support for biologics and small molecule drugs, across each phase of drug development. Our Total Quality Assurance (TQA) capabilities include proprietary method development, validation, method transfer, high throughput sample analysis. Specialising in PK, ADA, NAb & Biomarker based assays, utilising our wide range of platforms, such as the MSD S600, Quanterix HD-X, Gyros xPAND, Flow Cytometer, PCR, ddPCR, ELISA, LC-MS, NMR etc.

Analog Devices, Inc. (NASDAQ: ADI) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive advancements in digitized factories, mobility, and digital healthcare, combat climate change, and reliably connect humans and the world. We are at the forefront of an ecosystem that is driving healthcare forward to deliver life-changing solutions for all. Our technology captures clinical-grade data and turns it into simple, trusted insights for remote patient monitoring. We have decades of experience in the healthcare industry as a key technology provider for CT machines, MRI machines, digital x-ray, handheld ultrasound, vital signs monitoring, and much more. By making care possible in more places and delivering insight at the Intelligent Edge, we are helping to improve patient outcomes.

Learn more at www.analog.com and on LinkedIn and Twitter.

Komtur Pharmaceuticals is an international wholesaler and specialized service provider for the pharmaceutical industry. With branches and partners in every major market worldwide, we have built an unmatched global network to complement our long-standing reputation for innovative solutions, reliability in sourcing hard to find pharmaceuticals and getting medicines to patients in good time. It is our mission to support our partners in the pharma industry at any phase of the product life-cycle to bring their products to market and make them available to patients around the world, in-line with our vision to be the world’s most trusted patient-centric partner for the pharmaceutical industry. As an innovative, modern company, we are pleased to announce that Komtur Pharmaceuticals has successfully achieved certification as a Women's Business Enterprise (WBE) by WeConnect International. We are committed to promoting the value of women in the workforce and opening new avenues for growth and collaboration.

Because at our core, Komtur cares. Genuinely cares!

Almac Clinical Services currently provide services to over 600 Pharmaceutical and Biotech companies worldwide including the top 20 global pharma companies. Guided by our extensive clinical supply experience and expertise, we are recognised as one of the leading, multi-faceted, global solution providers within the niche and complex market of clinical trial supply. Utilising our best in house Supply Chain Management (SCM) expertise, custom designed services and software solutions, we offer the most flexible approach to support the delivery of your global clinical trial from protocol right through to patient delivery. Our core services are designed with flexibility to fit your clinical study requirements. From small-scale Phase 1 studies to international mega-trials, we have successfully managed thousands of protocols, bringing drug products to market faster and more efficiently.

OPIS was founded in 1998 by medical doctors from the Pharma Industry and is a Global clinical CRO with 25 years of experience in a wide range of therapeutic areas. OPIS provides full-service, 360° clinical trial support from study concept creation and protocol development to full project execution, study data handling and up to study closure, analysis, and reporting. We manage Phase I-IV, interventional, non-interventional and medical devices studies on an international level. In addition, OPIS also manages pre- and post-marketing clinical investigations for medical and diagnostic devices, nutraceutical, and food supplement studies.

Comac Medical is a comprehensive Contract Research Organisation (CRO) and Site Management Organisation (SMO), delivering clinical research services across 39 countries. Our dedicated professionals are committed to overseeing a broad spectrum of services from early to late phases, with a track record of over 1000 studies spanning 27 years. Drawing on extensive experience in therapeutic areas such as oncology, gastroenterology, dermatology, neurology, and more, we provide in-depth knowledge tailored to our clients' programmes and requirements. Comac Medical's Early Phase Unit brings over 18 years of specialised expertise to Phase I and Bioavailability/Bioequivalence (BA/BE) studies in Sofia. With a robust history of conducting more than 300 early-phase trials, our facility is the largest in Southeastern Europe and includes a Bioanalytical lab.

DHL is the leading global brand in the logistics industry. With approximately 395,000 employees in more than 220 countries and territories worldwide, DHL connects people and businesses securely and reliably, enabling global sustainable trade flows. DHL Life Sciences & Healthcare offers a comprehensive global logistics portfolio that is designed to meet the specific needs and challenges of the industry, with worldwide network operations, rigorous clinical and pharmaceutical governance, and incorporating high environmental standards. The DHL global network already connects tens of thousands of researchers, sponsors, and patients with compliant, safe, and robust distribution systems. Clinical trials logistics professionals can take advantage of these established, trusted DHL networks to reach out to patients, laboratories and researchers across the world. Ultimately, DHL delivers the vital logistics that ensure clinicians and researchers are able to complete their work, improving health outcomes for all.

BDD uniquely combines onsite CRO and investigative site activities at our clinical research facility based in a large research hospital in Glasgow, UK. By merging these functions, we offer our clients a comprehensive, integrated solution for early-phase clinical trials. Our streamlined process eliminates the need for coordination between multiple parties, providing more effective oversight, clarity, and control throughout your study. Located within our clinical facility, BDD houses a small scale GMP manufacturing suite. This allows us to manufacture your investigational product at a phase-appropriate scale and QP release onsite for same-day dosing to trial participants, saving significant time and costs in the early phase of development. BDD also offers adaptive clinical trials through integration of clinical research, GMP manufacturing, and formulation development into a single, cost-effective and efficient service. Recognising that one size does not fit all, BDD specialise in providing responsive, flexible, and innovative clinical trial solution for our clients.

Xerimis is a privately held clinical packaging and distribution firm specializing in the needs of medium and small pharmaceutical companies for phase I trials through phase IV global trials. Xerimis has focused on clinical packaging and distribution throughout our 22 years in existence. We have 3 wholly owned and managed depots; one near Philadelphia (US), one near Amsterdam (NL) and one near London (UK) as well as a network of audited and qualified depots strategically placed throughout the world.

QPS is a global, full service, GLP- and GCP-compliant contract research organization (CRO) delivering the highest grade of discovery, bioanalysis, preclinical and clinical drug development services. Since 1995, it has grown from a tiny bioanalysis shop to a full-service CRO with 1,200+ employees in the U.S., Europe and Asia. Today, QPS offers expanded pharmaceutical contract R&D services with special expertise in DMPK, toxicology, bioanalysis, translational medicine, and clinical research services. An award-winning leader focused on bioanalytics and clinical trials, QPS is known for proven quality standards, technical expertise, a flexible approach to research, client satisfaction, and turnkey laboratories and facilities. Through continual enhancements in capacities and resources, QPS stands tall in its commitment to delivering superior quality, skilled performance and trusted service to its valued customers. For more information, visit www.qps.com or email info@qps.com.

Climedo offers an all-in-one eCOA and EDC solution with hybrid capabilities for non-interventional studies and real-world evidence. By using a patient-centric approach and leveraging real-time data insights and visualizations around a study’s current progress, Climedo empowers its clients to better engage with healthcare professionals and other key opinion leaders (KOLs). This boosts awareness, stimulates scientific dialogue and accelerates the launch success of new medical innovations, thus reaching more patients faster. Founded in Munich in 2017, Climedo is a leading trusted partner for pharma, medtech, CROs and academia with over 1.7 million patients enrolled to date. Learn more at www.climedo.com.

Reducing Risk, Simplifying Supply, Elevating care

At Orifarm CTS, understanding that each patient is a real person beyond a number on a spreadsheet helps our team to focus on high quality and reliable sourcing of clinical trial supplies. With dedicated CTS teams and facilities in Denmark, UK, Czech Republic & USA we can ensure the optimal supply chain routing to meet for your requirements. We reliably deliver your clinical trial comparator and auxiliary medicines supply needs through data driven ethical sourcing practices with a focus on waste reduction and technology enabled sustainable supply chain processes, allowing you to focus on development of new treatments to patients. Patients are always at the heart of everything we do, because we care.

PCI is a leading global CDMO, providing integrated end-to-end drug development, manufacturing and packaging solutions to increase product speed to market and opportunities for commercial success. PCI brings the proven experience that comes with more than 90 successful product launches each year and over five decades in the delivery of supply chain healthcare services. With 30 sites across Australia, Canada, North America, the UK and Europe and over 4,300 dedicated employees, our mission is to bring life-changing therapies to patients. Leading technology and continued investment enable us to deliver development to commercialization solutions throughout the product lifecycle, collaborating with our clients to improve the lives of patients globally.

Suvoda is a global clinical trial technology company that specializes in highly complex, life-sustaining studies in therapeutic areas like oncology, central nervous system, and rare disease. Founded in 2013 by experts in eClinical technologies, Suvoda empowers clinical trial professionals to manage the most urgent moments in the most urgent trials through its IRT, eConsent, and eCOA solutions delivered on a single platform. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest, Romania and Tokyo, Japan. The company consistently boasts a customer satisfaction index of 9 out of 10, an NPS score of 70 in its annual surveys, and has been selected by trial sponsors and CROs to support nearly 1000 trials across 65 countries. To learn more, visit suvoda.com. Follow Suvoda on Twitter and LinkedIn.

Myonex is a global complete clinical trial solutions provider. For over 35 years, we have been the leading global clinical trial supply company and we have expanded our service portfolio to offer complete solutions around clinical trials for our partners. We at Myonex add value to our clients by helping them always be prepared for what is next in their clinical trials. Our goal each day, every day is to make sure our partners have whatever they need when and where they need it to execute a successful clinical trial, while also minimizing delays, unnecessary costs, and surprises.

Clinigen combines market-leading clinical trial supplies such as packaging and labelling, global storage and distribution, comparator sourcing, and biological sample management services. Part of Clinigen’s global supply chain facility and depot network, we deliver tailored solutions to ensure clinical trials are a success, regardless of the size, scope, or stage. We provide our clients access to 25+ years of clinical supply expertise and industry best cycle times.

N-SIDE is a software and service provider that enables organizations in the life sciences and energy industries to make better decisions and optimize the use of critical resources. We achieve this by combining deep industrial expertise with applied mathematics and AI. We have been an active player in clinical trial supply chain management for over 20 years and have 50% of the top 20 pharmaceutical companies as clients. With our SaaS-based software solutions and expert services, we streamline the clinical supply of pharmaceutical and biotech companies by accelerating clinical plans, mitigating risks, and curbing drug waste. We empower clinical supply leaders to make better, faster, and safer decisions for patients waiting for life-changing medications.