Claudio Semeraro is the dynamic Head of Candidates & Assets Supply at UCB Pharma, located in Braine-l'Alleud, Belgium. With over 15 years of rich experience in clinical trials, Claudio has mastered the art of clinical supply chain management. His expertise has been pivotal in coordinating and overseeing numerous clinical trials and supply operations. Claudio's passion for innovation shines through his active involvement in gene therapy projects, where he tackles challenges related to clinical and supply chain management with unwavering dedication. His relentless pursuit of excellence and commitment to advancing healthcare make him a true leader in the field.

Bliss Biomedics Clinical Research’s team is committed to carrying out creative and superior clinical trial studies for CROs and the pharmaceutical industry. Our Principal Investigators have great experience running clinical trials, from respiratory diseases, pulmonology, internal medicines, infectious diseases, vaccines, immunology and so on. Our site facilities are excellent, state of the art, and are ready to handle clinical trials for your organisation. We also have excellent access to patients’ database for clinical trials through our network of GPs and Private Practices. We would also like to collaborate with you on any of your clinical trials, as we are well positioned to do this seamlessly for you. We are ready to partner with you for your different clinical trials, from Phase 1-4. Our Capability Statement is available on request, which sets out our capabilities and therapeutic areas of expertise of our Principal and Sub Investigators.

Whether a pharmaceutical, biotech, or medical device company, we are your ideal mid-sized, full-service CRO. Our in-depth expertise and long-lasting experience combined with a flexible, and collaborative approach allow us to tailor our responses to each study. Our clinical development capabilities span through trial Phases I-IV, across a broad range of therapeutic areas including medical devices. We have an excellent track record for supporting a range of stakeholders in the pharmaceutical industry including sponsors and research institutions at each clinical development phase.

Veeva is building the Industry Cloud for Life Sciences. Our Clinical Platform helps the Pharma Industry to simplify and standardize clinical trials, for higher efficiency and a better experience for sponsors, sites, and patients. Our cloud-based solutions have helped hundreds of market-leading companies eliminate inefficiencies and bring high-quality, trusted, products to market faster without compromising safety or compliance.

Cryoport Systems is a comprehensive supply chain partner for the life sciences industry focused on meeting the challenges of the global cell and gene therapy market. We excel in the specialized management of the biopharmaceutical supply chain through our comprehensive offerings in logistics, BioServices and biostorage, cryopreservation, and consulting. Our expansive offerings are fully integrated to create a comprehensive platform that helps deliver risk mitigation, transparency, and certainty. With our expansive platform and decades of temperature-controlled supply chain expertise, Cryoport Systems helps Enable the Outcome for organizations from initial research through global commercialization.

The enterprise tech world is evolving with newer ambitions. While the wings of innovation are spreading to newer skies, the technologists are finding it hard to play catch-up and are making sure they are in tune with the technology juggernaut. CIOCoverage aims to bridge this very gap that exists between the tech-savvy where he rests, in the very heart of it. Awakening a keen insight in you to move along the flow, CIOCoverage works to make the entrepreneurs, versatile to the sturdy technological influences. We specialise in unfurling the latest and the voguish technology, conglomerating even the meticulous details from every arena of technology. We assimilate the most required ways of contemplation to guide our dear readers to make it to the top, briskly. We intend to incubate the technological sorcery and succour our elite readers to espouse the ‘learn-from-peer’ approach, to not only curb the U.S. market but also, create a big difference as an enterprise. CIOCoverage intends to bring all the aforementioned aspects together. The industry CEOs, CXOs and the CIOs are key decision makers in their respective organization, and they need to be aware and abreast of all the latest advancements and technological surges, while also be thoughtful of the impeding pain points and help themselves evolve different ways to address those. Our editions will bring together all such areas which are considered prominent, be its technologies such as AI, Big Data, Cloud and other novel trends, or in driving innovations and practices within.

Trialzen offers forecasting and planning solutions tailored to clinical trial supply management. Designed to minimize waste and optimize costs, our platform allows users to create custom forecasting models that align with trial schedules and manage supply budgets effectively. With optional RTSM integration and detailed reporting capabilities, Trialzen provides flexibility and precision in clinical supply planning.

Tive is the global leader in supply chain and logistics visibility technology. More than 850 global shippers, logistics service providers, and retailers use Tive to monitor shipment location and condition in real-time, gain actionable insights, and ensure end-customer satisfaction. Tive's cloud platform, patented sensor technology, and 24/7 Live Monitoring services reduce excursions and delays, minimize rejected loads, and decrease theft, damage, and spoilage. Customers count on Tive to ensure that shipments are delivered on time and in full—because every shipment matters.

Signant Health is the evidence generation company. We are focused on leveraging software, deep therapeutic and scientific knowledge, and operational expertise to consistently capture, aggregate, and reveal quality evidence for clinical studies across traditional, virtual, and hybrid trial models. For more than 25 years, over 600 sponsors and CROs of all sizes – including all Top 20 pharma – have trusted Signant solutions for remote and site-based eCOA, EDC, eConsent, RTSM, supply chain management, and data quality analytics.

Clinigen Clinical Supplies Management

True experts in clinical supplies. We accelerate your journey through clinical development so your product can reach more patients and touch more lives.

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...

Inceptua is a global pharmaceutical services company with market-leading capabilities across multiple business areas. We have over 25 years of experience serving life science companies of various sizes and global operations with offices across Europe, North America, and Asia. We provide clinical trial supply, services, and logistics, including comparator sourcing of medicines, packaging, labelling, storage, and distribution services. And we offer strategic advice, design, facilitation, and implementation of global early access programs, and distributes unlicensed and other medicines worldwide.

We explore how Artificial Intelligence and Exponential Technologies bring opportunities for people, organizations, and societies to increase their wealth and health. Our audience is anyone who wants to improve in their career, their business, their investments; who wants to live a healthier, more productive, and fulfilling life; who wants to simplify and improve the education systems of their communities, or who simply wants to understand how Exponential Technologies are changing the world. We publish articles, podcast interviews, and ebooks with insights from industry leaders and experts, and use cases of exponential technologies across multiple fields, including finance, healthcare, and education.

World Business Outlook is a Singapore-based business magazine. The website delivers all the latest global financial news and the latest insights, market views and industry talk from across the sectors. The magazine pages adorn the most innovative companies in its sector and opinions from the world's top business leaders. We get, on average, over 50k unique visitors every month. We have over 39 K followers on Facebook, 29 K followers on LinkedIn, over 25 K followers on YouTube and 5,930 followers on Twitter.

Endpoint Clinical is a leading clinical trial technology and service partner, delivering adaptable RTSM solutions with a focus on security, stability, and trust. With decades of expertise and a proactive, innovation-driven approach, Endpoint minimizes friction, reduces risk, and enables your teams to focus where it matters most—on trial success.

‘Medical Device Asia’ (MDA) is a leading bimonthly business publication for medical technology and healthcare. MDA has remained a key choice of the leading international exhibition organisers to promote their respective shows worldwide. MDA offers its readers latest updates on medical and health care technology by providing news, articles, interviews, new product launches, market reports, international events and much more. If you have any product, event or services to promote, please do not hesitate to contact us via email: info@medicaldeviceasia.in

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.

Suvoda is a global clinical trial technology company working to transform patients' experience in complex, life-sustaining studies in therapeutic areas like oncology, central nervous system (CNS), and rare diseases. Founded in 2013 by experts in eClinical systems, Suvoda empowers sponsors, CROs, sites, and patients to manage even the most urgent moments in the most urgent trials through advanced software solutions delivered on a single platform. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest and Iasi, Romania, and Tokyo, Japan. The company’s Net Promoter Score (NPS) consistently exceeds the technology industry average, contributing to the company being selected by trial sponsors and CROs to support more than 1,500 trials across more than 85 countries. Follow Suvoda on: LinkedIn.

4G Clinical’s suite of innovative RTSM and clinical supply optimization software provides the right-sized support for any phase or trial complexity. At 4G Clinical, all studies are supported by a team of RTSM experts to advise trial teams on the best path forward. Our operations team distinguishes itself through their extensive industry expertise and deep understanding of trial designs and mid-study adjustments. 4G Clinical is committed to helping sponsors and CROs follow the science, wherever it may lead, as quickly and as safely as we can. While we will not discover the next novel compound in the lab, we are doing our part by leveraging our extensive experience and technological innovations to bring speed and agility to clinical trials. As a critical partner throughout clinical development, we can help you seamlessly transition and scale your trials through both protocol and supply complexities to help bring crucial medicines to those who need them, faster.

We believe in the power of collaboration to unlock human potential and growth. We make collaboration better with growth-minded people and cutting-edge technology. Events are where people connect and everything can happen: learning, partnership, and growth. We are building tools for event organizers to seamlessly collaborate with speakers, partners, and sponsors. United we are stronger. Join us!

Comprehensive Pharmaceutical Solutions for Clinical Success

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.

Florence delivers a unified, digital infrastructure connecting Sponsors, CROs, and research sites for seamless clinical operations. As the leading site experience and enablement experts, we’ve designed technology that drives swift site adoption and simplifies workflows. Our SiteLink platform streamlines study startup, improves remote oversight, and accelerates collaboration—making trials more efficient and improving patient access. Trusted by top industry leaders, Sponsors have deployed our solutions at over 30,000 sites in 70+ countries. With Florence, you gain real-time visibility, robust compliance, and total control, enabling breakthrough research at global scale.

tempmate GmbH is a German expert with 40 years of experience in cold chain and supply chain monitoring. We work towards a loss-free supply chain to conserve our customers' resources by providing innovative environmental monitoring and data management solutions. With a dedicated team of experts, we continuously strive to develop our products and services to meet the changing requirements and standards in the cold chain and supply chain industry. We emphasize quality, precision and reliability to ensure that our customers can maintain their quality standards. Thanks to our extensive expertise and many years of experience, we have built up an impressive customer base and have become a trusted partner for companies from various industries all over the world. Our customers appreciate the cutting-edge technology, user-friendly handling and first-class customer service we offer.

Valos an international, specialized CRO, offers services for Phase I-IV Clinical Trials and retrospective studies. Our comprehensive resources include: Biostatistics, Data Management, Statistical programming, RWE and HTA solutions, GDPR & Auditing. Valos delivers effective results. Our experts guide you through the process with integrity, flexibility, commitment and dedication.

An international team specialised to the management and coordination of your Investigational Medicinal Products, Biological samples for your local and global clinical studies, offers you a personalised services through our integration platform LINCKIA.

Our services are aimed at Pharmaceutical and Biotechnology sectors.

THERADIS PHARMA SERVICES :

• Management of Investigational Medical Products: regulatory steps, sourcing of products, packaging, labelling, certification, documentation, storage, distribution, return, batch recall, destruction.
• Biological Sample Management: manufacture of sampling kits, sites equipment, training of investigation centre staff, pick-up of samples at the required temperature with transport partners, biological monitoring.
• Biobanking Services including receipt, verification, registration on dedicated software, short to long term storage, dispatch to worldwide laboratories.
• Management and Coordination of all supply chain actors.
• Randomisation and Trial Supply Management: services including methodological support, logistical optimization, study tracking with 24/7 support and real-time data integration with other third parties such as central labs, imaging, ECG, EDC, local depots…

Yoshe Clinical Operations LLC was founded with a clear vision — to revolutionize clinical research through innovation, expertise, and dedication. We are a team of seasoned professionals with decades of experience in managing complex clinical trials. Our mission is to deliver high-quality, timely, and cost-effective solutions tailored to the unique needs of our clients. Yoshe Clinical Operations was established to address the growing need for efficient and reliable clinical trial management. We understand the challenges that pharmaceutical companies, biotech firms, and medical device manufacturers face in bringing new treatments to market. That’s why we are committed to providing comprehensive support throughout the clinical trial process.

Catalent solves today’s clinical trial supply challenges and develops innovative solutions for the future. Catalent’s commitment to quality and service excellence is evident in its comprehensive and flexible solutions for small molecules, biologics and advanced therapy medicinal products (ATMPs). With modern global facilities, and 25+ years’ experience reliably supplying thousands of studies of all sizes and complexities around the world, services include:

• Clinical supply management
• Integrated formulation development, clinical manufacturing & blinding
• Specialty handling (potent, cytotoxic, controlled)
• Direct commercial product sourcing
• Clinical packaging/labeling
• Extensive clinical storage, cold chain capabilities & global distribution
• Demand-led supply
• Direct-to-patient solutions
• Clinical returns, reconciliation & destruction

Median provides best-in-class central imaging solutions for oncology clinical trials, empowering biopharmaceutical companies to accelerate the development and delivery of life-saving cancer treatments with unmatched operational excellence and reliability. And we don’t stop there. We are forging the way when it comes to innovative imaging technology, leveraging the latest in AI/ML-powered imaging intelligence to develop actionable insights for sponsors’ oncology programs worldwide.

Founded in 1997, Novotech is a global full-service clinical Contract Research Organization focused on partnering with biotech and small to mid-sized pharma companies to accelerate the development of advanced and novel therapeutics at every phase. Novotech has received numerous prestigious awards, including the Global Biotech Contract Research Organization Company of the Year Award 2024, 2024 Fierce CRO Awards for Excellence in Clinical Trial Management and Excellence in Global Operations, CRO Leadership Award 2023, the Asia Pacific Cell & Gene Therapy Clinical Trials Excellence 2023 and the Asia-Pacific Contract Research Organization Company of the Year Award 2023. The Company offers laboratories, Phase I facilities, drug development consulting, and regulatory expertise, and has experience with over 5,000 clinical projects, including Phase I to Phase IV trials. With 34 office locations and a team of 3,000+ professionals worldwide, Novotech is a trusted strategic partner of choice.

Efficiently recruit participants and execute trials with Studypages, seamlessly integrate data and tools, onboard sites with ease, and gain real-time insights into clinical trial operations using AI.

Bionical Emas is a global leader in Clinical Trial Supply (CTS) and Early Access Programs (EAP), committed to delivering life-changing medicines to patients worldwide. We partner with leading pharmaceutical and biotech companies to offer tailored solutions for their clinical trial needs. Our CTS division provides unmatched global access to medicines and ancillaries, leveraging a vast network of manufacturers and distributors, supported by an in-house Quality and Regulatory team. From local sourcing in emerging markets to global distribution of high-value commercial drugs, we deliver customized, end-to-end supply solutions. Our interactive CTS Sourcing Portal enables clients to manage and monitor their supply chain in real time, enhancing transparency and efficiency. With strategically located distribution centers across Europe, North America, LATAM, APAC, and Africa, we ensure timely delivery while meeting regulatory standards. Bionical Emas is dedicated to ethical, flexible, and reliable support for clinical trials worldwide.

At Biorce, we transform clinical trials with advanced AI solutions tailored to the pharmaceutical industry. Trusted by leading pharma and biotech companies, we empower professionals to design and execute trials faster and more efficiently. Our flagship product, Jarvis, is an AI-powered Clinical Trial Assistant that simplifies protocol design, optimizes workflows, and accelerates decision-making. With Jarvis, you can save up to 70% of your time and 50% of your budget during the trial design and research phase, all while maintaining the highest standards of data integrity and patient safety. Biorce brings together a multidisciplinary team of AI experts and clinical scientists to deliver innovative, compliant, and collaborative solutions. At the intersection of technology and healthcare, we’re shaping the future of clinical trials—ensuring groundbreaking treatments reach patients faster. Visit our website to discover how our transformative AI technology can revolutionize your clinical trials.

Intertek Pharmaceutical Services is a leading GxP-compliant contract research organization (CRO) providing expert analytical, bioanalytical, and clinical kit logistics solutions to the pharmaceutical and biotechnology industries. With a global network of laboratories and decades of scientific expertise, Intertek supports clients across the entire drug development lifecycle, from early-stage research to regulatory approval and commercial release. The company specializes in high-quality analytical services, including method development, validation, stability studies, and release testing for small molecules, biologics, and advanced therapies. Its bioanalytical services encompass PK, immunogenicity, biomarker, and cell-based assays to support preclinical and clinical studies. Additionally, Intertek offers clinical trial support through comprehensive clinical kit logistics services, ensuring efficient sample collection, management, and regulatory compliance for global studies. With a commitment to scientific excellence, regulatory compliance, and operational efficiency, Intertek Pharmaceutical Services is a trusted partner for pharma and biotech companies seeking high-quality analytical support to accelerate drug development and ensure product safety, efficacy, and quality.

Yourway, The Biopharma Services Company, is changing the landscape of clinical value-chain solutions with a unique, single source model. Yourway is the only truly integrated provider of clinical value-chain operations, from premium courier services and clinical packaging to drug product procurement to temperature controlled storage and transportation, and more. Supported by a global network of 19 GMP depots, Yourway has the resources and expertise to make your packaging and shipments faster, and management of clinical trials easier and more efficient. Yourway delivers a competitive advantage rooted in experience, trust, and a commitment to reliable global access for your clinical value-chain operations.

Linguamatics is a leading provider of AI-enabled language solutions for and by healthcare and life sciences. We empower clients to innovate at scale efficiently throughout the product lifecycle, from research and development to post-launch, ensuring compliance and patient-centric care across multiple languages and global markets.