GALSER is a Swiss-based clinical and regulatory partner supporting pharmaceutical and biotechnology companies with the execution and oversight of clinical trials. We focus on programs where Sponsors require close operational control, high-quality delivery, and a partner who can take full ownership of local clinical activities. Our experience team was involved in multiple clinical programs and supported over 15 projects spanning early to late clinical phases, as well as post-approval activities over the last five years. Our expertise covers clinical operations, monitoring, regulatory coordination, pharmacovigilance, and local trial execution, with a strong emphasis on quality and compliance. GALSER has built a well-established network of Swiss investigators and clinical sites, with a strong emphasis on close site collaboration, allowing us to manage full local operations efficiently. This integrated approach enables Sponsors to move quickly while maintaining robust oversight and regulatory alignment. Our vision is to operate with a partnership-driven model. Rather than applying standardized solutions, we tailor our support to the specific needs and constraints of each program, working closely with Sponsor teams to ensure reliable execution in complex clinical and regulatory environments. Our goal is simple: to help Sponsors advance their clinical programs efficiently, transparently, and with confidence.

Why Partner with Orifarm?

At Orifarm Clinical Trial Supplies (CTS), we take care of your sourcing requirements, work to understand your specific needs, and offer unrivaled product access for clinical trial use. With locations in both Europe and the United States, Orifarm can source drug from a variety of locations with more cost-effective options.

• Established supply chain network in US & EU
• Dedicated global procurement team
• Unparalleled access to large quantities of product
• Over 150,000 sq. ft. of inventory holding space
• More than 4,500 sq ft. in cold room storage
• 250+ approved suppliers across 27 markets

Urgent Need Capabilities:

If you have an “urgent” small to moderate quantity product requirement, we often have the ability to accommodate your needs from our existing warehouse inventory.

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Our Team combines years of experience on the delivery of products for clinical trials along with a diverse range of prior experience in parallel industries and extensive research activities.

Established in 2004, Oximio is a leading provider of supply chain solutions for clinical trials, bringing 20+ years of industry experience and expertise to the global clinical research industry. Employing over 300 highly skilled, multi-national employees, it provides innovative, tailor-made solutions to deliver outstanding quality, customer service at all times, ensuring the highest operational standards. Our clinical trial supply chain is built to meet the demands of complex, multinational clinical studies across the globe. With UK headquarters, the company also benefits from its wholly owned depots in Europe, MENA, Africa and North America. A comprehensive partner depot network further expands the company’s reach to effectively meet the demands of global, clinical trial requirements. Our cold-chain logistics services offer inbound and outbound shipping services, Importer of Record (IOR), re-labelling, returns/accountability, medicine destruction, and direct to site and direct to patients solutions in addition to comparator sourcing. Explore our complete range of supply chain solutions at Oximio.com.

Kinaxis is a global leader in modern supply chain orchestration, powering complex global supply chains and supporting the people who manage them, in service of humanity. Our powerful, AI-infused supply chain orchestration platform, Maestro™, combines proprietary technologies and techniques that provide full transparency and agility across the entire supply chain — from multi-year strategic planning to last-mile delivery. We are trusted by renowned global brands to provide the agility and predictability needed to navigate today’s volatility and disruption. For more news and information, follow us on LinkedIn.

Nuvisan is a full-service contract research organisation (CRO) and development and manufacturing organisation (CDMO) with state-of-the-art laboratories in Germany and France. Our pharmaceutical, biotechnology, venture capital and non-profit clients partner with us because our high-quality end-to-end solutions and scientific expertise enable us to streamline and accelerate drug discovery and development – from ensuring target understanding to helping bring therapeutics to life. Founded over 40 years ago by a team of pharma industry innovators, Nuvisan has established a reputation for expertise and professionalism. Our team leaders have extensive experience in the biopharma industry, and our unique centers of excellence – for drug discovery in Berlin, formulation and GMP manufacturing in Sophia Antipolis, and our bioanalysis hub in Neu-Ulm – enable our experienced scientists to help guide and advance projects. We know how to discover, develop and bring the next generation of medicines to market. At the same time, we are committed to flexibility, transparency and collaboration in our approach, working closely with you to adapt to your individual needs, minimise risks and help deliver your project.

At Catalent, we champion the missions that matter to help people live better and healthier lives. Every medicine, therapy and product that we help develop, manufacture and deliver is part of our commitment to put patients first in everything we do. We are a trusted partner because we are committed to an exceptional, high-quality experience. Our customers turn to us for tailored solutions to meet their needs as we work together to transform lives.

Inceptua is a global pharmaceutical services company with market-leading capabilities across multiple business areas.

• Inceptua Clinical Trial Supply and Clinical Services provides clinical trial supply, services and logistics, including comparator sourcing of medicines, packaging, labelling, storage, and distribution services.
• Inceptua Early Access offers strategic advice, design, facilitation, and implementation of global early access programs, and distributes unlicensed and other medicines worldwide.

Inceptua has over 25 years of experience serving life science companies of various sizes, and has global operations with offices across Europe, North America and Asia, including China.

Founded in 2001, Richmond Pharmacology is a leading Contract Research Organisation (CRO) with a heritage in first-in-human and adaptive clinical trials. It has conducted around 20% of all UK Phase I studies and ran the first clinical trial in which a CRISPR therapy was delivered through the bloodstream to edit genes inside the human body. Today, Richmond supports global pharmaceutical, biotech, and genetic engineering partners, including several top 10 pharma companies, in advancing next-generation therapies. In 2020, it established the Richmond Research Institute to expand understanding of under-researched diseases. Building on its early-phase leadership, Richmond Pharmacology is focused on advancing smarter, more adaptive and patient-centric clinical development. By integrating innovative trial designs, real-time data insights and operational excellence, Richmond helps sponsors navigate complexity and accelerate critical development decisions. Its collaborative approach reflects the evolving future of clinical trials, one driven by innovation, efficiency and meaningful impact for patients.

Quipment is a leading player in clinical trial equipment solutions - rental, sales, and inventory management—for CROs, pharma, and biotech. We manage global deployment and support throughout the entire clinical trial process, operating across 110+ countries from our technical service centers in France, the US, and Japan. All devices are checked, calibrated, and controlled by in-house experienced biomedical technicians to ensure precision and performance at every stage of the study. Our circular model limits waste and reduces the carbon footprint of clinical trials, while our flexible approach adapts to each project’s specific needs. As a mission-driven company, we integrate sustainability, ethical responsibility, and innovation into our operations. The underlying force behind every clinical trial, whatever the need, Quipment makes it possible.

Euromed Pharma is the healthcare global service provider company of Petrone Group with branches in 10 countries. It supports pharmaceutical and biotech companies with strategic, end-to-end solutions for Clinical Trials, from early planning to expert comparator sourcing and streamlined logistics.

• Comparator sourcing, by providing Comparators, branded and generics; Ancillary materials; Rescue medications; Concomitant and background medications, and by acting as an Importer of Records (IOR) bridging customs authorities and customers. By managing regulatory and logistical complexity, Euromed Pharma enables sponsors to focus on trial execution rather than supply constraints.
• Integrated IMP Management model supports clinical supplies needs while improving cost control and operational performance:
  • Placebo manufacturing, primary and secondary packaging, and labelling at 15-25°C, cold and negative temperatures
  • GDP-compliant storage and global distribution from ambient to -80°C
  • Temperature-controlled and cold-chain logistics to ensure product integrity
  • End-to-end supply chain visibility and oversight

Euromed Pharma simplifies complexity, so your clinical trials run smarter, faster, and safer.

Endpoint Clinical is a trusted clinical trial technology and service partner that delivers reliable RTSM solutions. Endpoint blends seamlessly into clinical trial processes by providing anticipatory and adaptive solutions to proactively mitigate risks. With decades of experience, Endpoint offers a deep understanding of the challenges sponsors and CROs face. Its tech-forward dedication to innovation and high-touch services enables Endpoint to control the controllables and proactively generate speedy, strategic solutions so sponsors and CROs can focus on running seamless clinical trials.

NextPharma is a leading European pharmaceutical Contract Development and Manufacturing Organisation (CDMO) with current five sites in Germany, two in France, one in UK, one in Norway and one in Finland. NextPharma supplies Pharmaceutical and H&N products globally. With expertise in solids, semi solids and non-sterile and sterile liquids, the company provides services from pharmaceutical development, clinical supplies, scale-up and process validation through to commercial manufacturing for a large range of dosage forms. NextPharma’s expertise enable it to provide a unique service offering in certain very specific specialised areas such as hormonal solids and semi-solids, cephalosporins, penicillins, narcotics, modified release products, ophthalmics as well as paediatric medicinal products.

OCASA is a global company leading in logistics solutions, continually expanding its reach. With over 40 years of solid experience, the company demonstrates its ability to evolve, innovate, and deliver solutions for the pharmaceutical industry in every operation. Its services are designed to adapt to each stage of the clinical process, offering personalized responses to every client. At the heart of every OCASA operation there is a youCentric approach, which reaffirms their commitment to human life behind the clinical process. Every patient represents a unique and valuable life. The core of the logistical operation transcends efficiency, it is about delivering hope.

Medable is on a mission to get effective therapies to people faster. Its ai-powered clinical trials platform enhances speed, scale, and patient access in clinical research, accelerating medicines for thousands of conditions without treatment or cure. Awarded Best Digital Health Solution by the Galien Foundation and ranked Leader in eCOA by Everest Group, Medable’s platform has been deployed in nearly 400 trials in 70 countries and 120 languages, serving more than one million patients globally.

KLIFO is an EU full-service provider of clinical trial supply (CTS) packaging, labelling and distribution services. Since our formation more than 20 years ago, KLIFO’s CTS business has grown consistently based on our strong reputation and loyal client base. In September 2025 we moved to our new 6,500 sq m (65,000 sq ft) facility in Denmark, which further enhances KLIFO’s ability to support our client’s clinical trials from Phase I through to product approval and registration. KLIFO currently supports more than 100 biotech and pharma clients globally. Our growth has been built on the experience and expertise of our team, many of whom have sponsor-side experience of the challenges associated with outsourcing CTS projects. Our flexible and fast-turnaround service has been developed based on this experience – to make management of outsourced CTS projects as reliable and hassle free for our clients as possible.

Suvoda is a global clinical trial technology company with a real-time experience platform that empowers sponsors and CROs to make confident decisions and sites and patients to take calm, controlled action. Suvoda delivers interconnected, action-driven software solutions and industry-leading services and support, so that even in the most time-sensitive, mission-critical moments, life-changing studies keep moving forward. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest and Iasi, Romania, and Tokyo, Japan. The company maintains customer satisfaction scores that consistently exceed the technology industry average, contributing to the company being selected by trial sponsors and CROs to support more than 2000 trials across more than 95 countries. Suvoda recently merged with Greenphire, a leading provider of clinical trial financial management and patient support tools. To learn more, visit our website and follow Suvoda on LinkedIn.

Envirotainer transports life-saving pharmaceuticals globally with innovative temperature-controlled solutions. We have led the industry for 40 years and offer the widest choice of cold chain solutions. Our shipment monitoring services backed by our extensive global network get your product to where it needs to be, precisely when it needs to be there. We ensure the safety and efficacy of medicines for the pharmaceutical life cycle, from R&D all the way to commercial distribution, and our ambitious science-based targets help us reduce not only our emissions but our customers', too. For more information, please visit our website.

4G Clinical is dedicated to bringing crucial medicines to those who need them, faster. By revolutionizing RTSM (randomization and trial supply management) and clinical supply optimization software, 4G Clinical provides the right-sized support for any phase or trial complexity. Our innovative solutions, including Prancer RTSM速 and 4C Supply速, are designed to tackle bottlenecks in clinical trials, accelerating research by disrupting traditional execution methods. At 4G Clinical, we support all studies with a team of RTSM experts who advise trial teams on the best path forward. Our operations team distinguishes itself through extensive industry expertise and a deep understanding of trial designs and mid-study adjustments. As a critical partner throughout clinical development, we help sponsors and CROs seamlessly transition and scale trials through both protocol and supply complexities. To learn more about our innovative solutions and how we are accelerating clinical trials.

MEDAIR GLOBAL is a full service, biopharma specialist, time and temperature controlled, global express delivery services provider with proven, flexible services for all INCO Terms, operating significant fleets of validated, globally positioned, TC shippers along with ambient and TC vehicles across, our well established, qualified, QMS managed International Office and Service Partner Network for all biopharma time and temperature sensitive logistics requirements from worldwide to worldwide. Our expert, trained and qualified staff deploy leading edge, qualified TC shippers, packaging materials and coolant systems for all TC ranges from +15C to +25C, +2C to +8C. -20C, -70C to -80C and cryogenic LN2 Dry shippers for door to door worldwide services supported by continuous real-time, in-transit shipment monitoring so that you can be certain of secure and consistent, on-time and in-temperature delivery whenever and wherever you use MEDAIR GLOBAL. MEDAIR GLOBAL Your Trusted Cold Chain Shipping Services Partner.

As a global CDMO with sites in Germany and the US, we specialize in developing and manufacturing innovative pharmaceutical products, focusing on solid oral dosage forms like powders, pellets, and granules. Our expert team optimizes formulations and processes, ensuring clinical trial success within timelines and budgets. We provide end-to-end Clinical Trial Supply (CTS) services, including placebo production, blinding, packaging, and labeling for semi-solids, liquids, and medical devices. Our capabilities span ambient, cold chain, and ultra-cold storage, supported by a global GMP network and IRT technology. Our agile project management ensures flexibility for global trials from Phase I to Phase IV. We also offer customized packaging solutions, Comparator and Co-Medication sourcing, and Importer of Record (IOR) services for seamless, compliant imports. With a commitment to excellence, we empower pharmaceutical companies to focus on innovation while we handle the complexities of clinical trial logistics.

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

Resonant Clinical Solutions delivers end-to-end clinical trial and diagnostic services designed to accelerate science. Building on a strong legacy in life sciences logistics, we provide comprehensive solutions that go beyond supply fulfillment—offering agile collaboration and personalized support as an extension of your team. Our expertise spans biorepository management, custom kitting and global logistics, and equipment & ancillary services, ensuring every detail of your research workflow is handled with precision. From procurement and delivery to calibration and recovery, we simplify complex processes while maintaining strict compliance with international standards. With strategically located service centers and a global partner network, we combine technical and regulatory insight with proven experience to serve customers worldwide. At Resonant Clinical Solutions, we’re committed to problem-solving, innovation, and helping research and clinical teams move science forward.

At RxSource our passion is to improve the lives of patients. As a provider of clinical trial supply services to the global pharmaceutical and biotech industry, we strive to achieve the extraordinary by offering industry-leading timelines for clinical trial supply projects. Our portfolio of services include; sourcing of commercial products (comparator, co-medications, rescue medications, ancillaries), packaging and labelling of clinical trial supplies within temperature-controlled conditions (ambient, refrigerated and frozen), global temperature-controlled distribution of clinical trial supplies through our North American and EU facilities along with our global network of partner depots, Importer of Record, and QP release services (EU), including consultation of complaint and tax-efficient movement of clinical trial medications. Our passion, coupled with our can-do attitude, experienced team, flexible capacity planning and goal to impact the lives of 10 million people positively, makes us different. When you partner with us, your trial is our passion.

NeSPaT has been providing patient travel and reimbursement services since 2013, combining deep local expertise with wide regional coverage. With a multinational team and a focus on digital innovation combined with a human approach, NeSPaT streamlines patient logistics, offering tailored services, 24/7 support, and seamless documentation management.

La Gazette du LABORATOIRE is the Meeting Place for all Players in the World of Laboratory and Science

Created by a scientist, La Gazette du LABORATOIRE has been supporting the life of the French Research, Development, Analysis and Control laboratories since 1995. In our France edition, our Africa edition, and on our websites www.gazettelabo.fr and www.LABORATOIRE.com, you will find:

• specific articles and contents
• resources for your daily work
• practical and technical advice
• business testimonials, trainings, job announcements
• information on events related to the field of laboratory and science
• tools to communicate on your news, your projects and increase your notoriety

La Gazette du LABORATOIRE, a human-sized team at your service - for any question: contact us! or call us +33 (0) 4 77 72 09 65

Pharmaxess Consulting helps biotech companies and investors unlock the full value of their innovations through a Value & Access strategy. Represented by Clémentine LAURENT, a scientist with over 10+ years in biotech and 5+ in Market Access, the firm combines scientific expertise with a strong business mindset to bridge development, evidence, and market realities. It supports clients from early development to commercialization, aligning clinical and access strategies, engaging key stakeholders, and defining clear value and ROI. Pharmaxess Consulting anticipates payer and patient expectations and designs realistic pricing and reimbursement strategies that maximize both impact and sustainability. Its mission is to turn great science into accessible, valuable healthcare solutions by connecting development choices with future access success.

Life Science Review Magazine is a print and digital magazine with a total subscription of 124,000 qualified subscribers consisting of senior decision-makers from Pharmaceutical, Biotech, Medical Device and Diagnostic space performing functions in Sales & Marketing, Manufacturing, Supply Chain, R&D, Clinical Operations, Finance, and HR. It provides a comprehensive platform for senior-level industry experts, acquirers, and decision-makers to share their insights following a unique peer learning approach.

Almac Clinical Services have been partnering with clients for 30+ years, we set the standard for developing effective supply chain strategies that ensures our sponsors can overcome their unique challenges and deliver supply continuity to patients wherever they are in the world. We have a range of tools and services to help you achieve this, from forecasting/inventory management, supply chain strategy to global logistics management, end-to-end temperature solutions, IRT set-up and strategy, direct to patient distribution and pharmacy services alongside our clinical packaging and labelling facilities. When you partner with Almac you are partnering with experts who Supply with Care™.

CN1699 is a global medical media platform connecting academia, healthcare institutions, and industry professionals through multilingual news, academic content, and digital outreach. With active networks in Asia, Central Asia & the Caucasus, the Middle East, Europe, and Africa, it supports over 500,000 healthcare users. Key services include the MDLA Digital Library, offering academic resources to universities and libraries, and WeMed, a collaboration program linking medical schools, events, and experts worldwide. As an official media partner for international healthcare exhibitions, CN1699 provides bilingual promotional support through its websites, newsletters, and social media, helping events and organizations achieve targeted visibility and academic impact across global medical markets.

LABePEDIA is a Global B2B Platform for Selling and Sourcing Laboratory Equipment For Education, Scientific Research, Medical & Engineering Industries. If you are a manufacturer / distributor of laboratory equipment for education, industry or research then LABePEDIA can offer you many opportunities. As a member of LABePEDIA you are exposed to global buyers / sellers of laboratory equipment. Since LABePEDIA is a specialized platform for the laboratory equipment community; only verified companies / individuals can be a part of this esteemed group.

BPT Analytics (BiopharmaTrend) delivers pharma and biotech news, industry reports and interviews with key experts, along with technology scouting and market research services. We are exclusively dedicated to exploring the advent of novel technologies in life sciences and all things 'tech & bio.'

Mediaplanet are running a Future of Clinical Trials campaign launching on the 12th December through the New Scientist magazine, with extended distribution via social and events. The campaign aims to drive forward-thinking dialogue and actionable insights that ensure clinical trials are more efficient, inclusive, and patient-centric, accelerating progress in delivering better treatments and medical devices for global health needs in a rapidly evolving landscape. To find out how you can be involved, please email Anokhi.shah@mediaplanet.co.uk.

Inato is on a mission to bring clinical research to every patient, regardless of where they live. The global technology company combines trial planning, site selection, and patient pre-screening into a single AI-enabled platform to transform the way research sites and sponsors work together to advance medical research. Leading pharmaceutical companies trust Inato to enhance trial accessibility and representation, and thousands of research sites leverage the platform to find the right research opportunities for their communities and streamline trial operations.

Founded in 2000 by industry leaders, SanaClis was among the first providers to combine Clinical Supply Chain and CRO services across Europe. Over the past 20+ years, we have expanded globally, covering Europe, North America, LATAM, APAC, and South Africa. We have successfully delivered projects for sponsors ranging from virtual biotechs to top 10 pharmaceutical companies. Notably, over 93% of studies under our management were completed on or ahead of schedule and on budget. SanaClis offers a comprehensive range of CRO and Clinical Supply Chain services across all therapeutic areas, phases, and major geographies. With deep expertise in Central and Eastern Europe, we deliver added value through high patient enrollment rates and high-quality data. Our flexible Full Service and Functional Service models allow sponsors to streamline studies. In addition, we own a portfolio of GMP and GDP certified storage and distribution depots, supported by a qualified global depot network.

At Biorce, we help pharma and biotech companies run faster, smarter, and more cost-effective clinical trials using advanced AI. Our flagship platform, is the first AI Clinical Trial Assistant built to accelerate protocol development, feasibility, and study startup. It reduces amendments, improves patient matching, and supports more confident decision-making—leading to faster timelines and lower risk. Designed with input from leading clinical experts, Biorce’s platform transforms regulatory data and medical literature into actionable insights that streamline planning and execution. Whether you’re a global biopharma, an agile biotech or a CRO, Biorce helps your teams design better trials and bring treatments to market sooner. We bring together expertise in AI, clinical operations, and healthcare to solve today’s biggest R&D challenges, without compromising quality, compliance, or patient safety.