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Lumis International GmbH supports non EU-biopharmaceutical companies as their legal representative. Through their daughter company Lumis Life Science Consulting GmbH they provide customer-tailored consulting and solutions for clinical vendor selection and management, clinical trial oversight, quality management, and training. Jointly with our customers, we develop tailored solutions to optimise their clinical development program. We collaborate with a network of experienced subject matter experts, cooperation partners, and consultants.

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To learn more , please visit our website - www.lumisinternational.com

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At Trilogy, medical writing is our passion. As specialists in clinical regulatory documentation, we provide a service that is more than just writing. We proactively plan, coordinate and write clinical documents to meet timelines, with a readability that reduces the time for review and approval.

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To learn more , please visit our website - https://www.trilogywriting.com/

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Frontage is a CRO providing integrated, scientifically-driven research, analytical and product development services throughout the drug discovery and development process to enable biopharmaceutical companies to achieve their drug development goals. We are focused on helping our client’s to address their most significant and complex drug discovery and development challenges. Our scientific knowledge base, technical expertise and reputation for high quality services have been integral to our ability to turn our services into your solutions.

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To learn more , please visit our website - www.frontagelab.com

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For over 30 years BURG Translations has been providing high-quality, certified clinical trial translation services in over 300 languages. Our clients are leading pharmaceutical, medical device and clinical research organizations (CROs), including Abbott, Takeda, Quintiles (now IQVIA), US Oncology, BRANY, ICON, Clinical Logistics and more.

We translate a variety of medical documents, from protocols and pharmacological studies to informed consent forms (ICF), patient questionnaires, sales and marketing materials, and interactive solutions such as videos.

We are ISO 17100:2015 certified and provide complete end-to-end language solutions, from preclinical to regulatory submission (FDA/EMA compliance) and go-to-market.

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To learn more , please visit our website - http://burgtranslations.com/

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To learn more , please visit our website - https://www.huma.com

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Axiom is celebrating 22 years of delivering hundreds of studies in dozens of countries. Since its founding in 2001, Axiom has delivered data-driven, powerful, and cost-effective eClinical Solutions and Services dedicated to small-to-medium life science companies. Axiom Fusion eClinical Suite is the most adaptable, Unified Platform that serves as the Connected Hub for all your Clinical Trial and operational data and reporting. Choose from 15+ unified modules on a single platform: EDC, DM, RTSM/IRT, CTMS, Inventory Management, ePRO, eConsent, Patient Portal, AE/SAE Tracking, Safety Database, Central/Local Lab, Imaging Management, eTMF, and 24/7 Project and Clinical Data Reporting. We are an embedded partner dedicated to the success of your study, offering managed services such as: Data Management, On-Demand Data Analytics, Biostatistics, Clinical Management, eTMF Management and Pharmacovigilance.

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To learn more , please visit our website - https://www.axiommetrics.com

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Medrio is the leading provider of eClinical technology for pharma, biotech, device, diagnostics, and animal health clinical trials. Founded in 2005, the company’s cloud-based EDC, Direct Data Capture, eConsent, and ePRO solutions deliver fast, flexible, and easy-to-use tools for the collection and management of clinical data and patient reported outcome responses. Study sponsors and contract research organizations have used Medrio extensively in clinical trials across a wide array of therapeutic areas, with notable success in oncology, infectious disease, and more. Medrio has extensive experience in all study phases and leads the market in early-phase trials. The company serves over 600 customers globally, with headquarters in San Francisco and offices in numerous domestic and international locations.

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To learn more , please visit our website - https://medrio.com/

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Clinical Services International (CSI) is a global leader of sourcing and management of commercially available medicines (comparators, concomitant medication) for clinical trials.
Headquartered in London and with operations in UK, Germany, Denmark, Japan and USA, we provide efficient solutions and serve worldwide trials. Our longstanding experience and relationships with manufacturers, enables us to provide custom made solutions to address the most complex requirements.
We accelerate drug development and reduce timelines by providing a fully integrated service.
Address Regulatory, Quality, Operational, Clinical requirements
Manage the entire supply chain and offer tailor-made solutions
Comprehensive expertise in Oncology and Biosimilar products.
Advanced Technology and Innovative approach
Trusted partner of leading Biopharmaceuticals, CROs and CMOs.
www.csint.com

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To learn more , please visit our website - www.csint.com

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APICES provides full range of clinical research services improving the quality of investigational products development optimizing the processes and activities of clinical research from project design to the publication of results, with expert project management that avoids and anticipates with contingency plans any possible deviation from the original project goals.

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To learn more , please visit our website - www.apices.es

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To learn more , please visit our website - http://www.excelya.com

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We’re more than a supplier: we’re a partner that can deliver consistent quality and superior service, a partner that fuel innovation for foster real and sustainable results. A deep understanding of healthcare industry and our customers’ needs is critical to ensure our range of packaging products and services deliver value through the entire product lifecycle. These insights and the experience of the WestRock Adherence team enable us to work in tune with regulations and clients to provide a service solution underpinned by an innovative and unparalleled range of packaging products including Clinical Trial Packaging, specialty labels, literature & booklets, Adherence packaging, multiple component kits and SMART Digital Adherence Technology.

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To learn more , please visit our website - www.westrock.com/markets/healthcare

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Howden is a major manufacturer of gas and air handling equipment. We have been designing and manufacturing ventilation fans for tunnel applications since the 1920’s under a range of legacy and current product brands and have a global installed base. Our expertise has developed considerably, starting at concept by enabling the optimisation of system design and continuing throughout the lifetime of operation using leading modelling (Ventsim), fan (axial and jet) and digital technology (Uptime) to deliver a truly end-to-end solution.

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To learn more , please visit our website - www.howden.com

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Since 1997, Clinigen has offered market-leading clinical trial supplies and biological sample management services to meet the most complex clinical supply challenges. Part of Clinigen Group’s global supply chain facility and depot network, we deliver tailored solutions for clients to ensure their clinical trials are a success, regardless of size or scope, from Phase I to Phase IV projects.

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To learn more , please visit our website - www.clinigencsm.com

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To learn more , please visit our website - http://www.ancillare.com/

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assisTek has been paving the way for integrating technology and data collection in clinical trials for over 25 years. We have earned a solid reputation around the globe by delivering customized solutions used in over 500 clinical research trials, across 90 different languages in 80 different countries. Based outside Philadelphia, Pennsylvania, we pride ourselves on being boutique by design and always customer focused. eCOA is our core focus but not our only service. Our experienced team has been in this niche of clinical research with deep domain experience for decades and client solutions has been our passion for over two decades.

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To learn more , please visit our website - www.assistek.com

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EMIS Recruit is an integrated solution that connects Research, Life Sciences and healthcare by embedding clinical research recruitment tools directly into the point of care systems. EMIS recruit gives research organisations clear visibility of clinically relevant patients based on your study protocol. This enables us to provide you with qualified patients that streamline your recruitment process

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S-Clinica offers VISION, a unique platform for the anticipatory management of your clinical trials.

From study concept to study closer, our system will help you handle your mission, smoothly and stress-free.

Say goodbye to drug wastage, patient loss, or recruitment delays. A team of our experts will guide you along the way!

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To learn more , please visit our website - http://www.s-clinica.com

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4Pharma is a specialized CRO with unique niche competence in biostatistics and data management. Since 2002 the company provides services to pharmaceutical, biotechnology, medical device and food companies. With offices in Finland and south of Sweden, the company offers local Nordic expert collaboration both with the industry and clinical CROs.

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To learn more , please visit our website - http://4pharma.com/

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Handbook

Building on our world-renowned Outsourcing in Clinical Trials conference series, Arena International seeks to deliver cutting-edge content on how best to manage and strategize your clinical trial in the 2023 edition of our annual handbook. Please read it here.

This issue of the OCT Handbook looks at how the industry has grappled with the challenges 2022 has brought – in particular, how the sector is moving on from the fallout of the COVID-19 pandemic and the impact of the Russia- Ukraine conflict on running clinical trials. This edition includes chapters on key industry themes including: Direct-to-Patient and Decentralized clinical trials; diversity and inclusion in clinical research; and the latest in clinical technology and innovation.

Comprising industry-written insights and specialist analysis, the handbook also includes a comprehensive supplier directory, providing readers with a one-stop shop for sourcing vendors to meet their operational needs. With this and so much more inside from our sponsors, we hope you enjoy the latest edition in Arena’s growing handbook series.

Articles you won’t want to miss include: