LSK Global PS delivers a comprehensive, end-to-end clinical development model built on 26 years of industry experience, aligning strategy, operations, data, and regulatory functions to minimize delays, reduce risk, and ensure quality. Unified workflows across clinical operations, data management, and biostatistics enable efficient execution and timely submissions, while pharmacovigilance and medical writing are seamlessly incorporated to support submission-ready deliverables. Combined with academic and epidemiological expertise and extensive domestic and global trial experience, this approach strengthens regulatory readiness and supports successful clinical development in Korea.
INTERTEK
We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance Provider to industries worldwide. With over 40,000 employees in over 1,000 locations in 100 countries, our network of science-based, highly technically skilled individuals and teams enable global and local businesses to overcome the complex quality, safety and sustainability challenges they face, every day. | Intertek is a global leader in product assurance, testing, inspection, and certification. We provide safety and performance testing and certification to help manufacturers meet regulatory requirements, industry requirements, customer specs, or to prove marketing claims about the product. Learn more at www.intertek.com. | Intertek’s Building and Construction division is a suite of Intertek brands that are industry leaders across multiple architecture, engineering and construction disciplines, developing the most innovative product and project solutions.Our experienced staff and comprehensive range of product-related testing and certification capabilities ensures that our clients have a clearly defined path to market, with cost-effective solutions and the ability to operate with pace and precision. Intertek’s project-related assurance, testing, inspection and consulting services are the risk management and quality assurance partner you need to ensure the reliability, safety and performance of your new developments, existing assets and facilities. | Intertek is a global leader in battery testing and certification, conducting over 20,000 evaluations annually across all battery chemistries and sizes, from button cells to EV and grid storage. Backed by a global network of 1,000+ accredited laboratories, we deliver customized Assurance, Testing, Inspection, and Certification services. Trusted by top manufacturers worldwide, our science-based testing ensures products meet stringent quality, safety, sustainability, and performance standards. With precision, pace, and passion, Intertek helps clients navigate regulatory requirements and confidently enter global markets. | Intertek is the worldwide leader in delivering complete quality assurance services to manufacturers throughout the information and communication industry. For decades we have provided the industry with specialized performance testing and independent verification, offering an unsurpassed suite of services to address the needs of the industry. Intertek is a trusted partner in helping ICT companies develop and launch products with less risk, greater quality, and increased revenue potential. | Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification solutions for our customers’ operations and supply chains. For Total Quality Assurance across safety, performance, and energy efficiency, Intertek has the expertise to quickly bring lighting products to global markets. With a heritage born from Thomas Edison in 1896, we have built an international business model designed to get your high-quality products to market faster than the competition. | Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries delivers innovative and bespoke Assurance, Testing, Inspection and Certification solutions for our customers’ operations and supply chains. Leading appliance and electronics manufacturers rely on Intertek for comprehensive testing and certification services, ensuring compliance with global standards for safety, performance, energy efficiency, and more. | Many countries worldwide have adopted compliance requirements and regulations to help ensure the safe use of FCMs. Our team of experts can help manufacturers comply with global industry regulations and standards to expedite market entry, while ensuring the quality and safety of their FCMs. Acting as a 3rd party in the value chain, we will help you coordinate information between business partners, evaluate formulations under NDAs, conduct compliance and analytical testing to ensure compliance of the evaluated products. | Intertek Allentown is an ISO 17025 accredited laboratory that provides advanced analytical tools and expertise for chemicals, materials and product testing, and research & development. Quality and reliable testing services for global compliance and quality control needs. | Intertek is a global leader in battery testing and certification, conducting over 20,000 evaluations annually across all battery chemistries and sizes, from button cells to EV and grid storage. Backed by a global network of 1,000+ accredited laboratories, we deliver customized Assurance, Testing, Inspection, and Certification services. Trusted by top manufacturers worldwide, our science-based testing ensures products meet stringent quality, safety, sustainability, and performance standards. With precision, pace, and passion, Intertek helps clients navigate regulatory requirements and confidently enter global markets. | Intertek delivers global testing and certification solutions for Transmission and Distribution Equipment (TDE). Supporting IEEE, IEC, and UL standards, we help manufacturers and utilities validate safety, performance, and compliance while accelerating time to market. | Did you know Intertek is behind the safety of toys in different parts of the world? Intertek assures the quality, safety, sustainability and performance of all categories of toys while facilitating their global market access to over 50 major markets in the world. Learn more: https://www.intertek.com/toys-childrens-products/
Insuvia
Insuvia is a trusted partner for biotech companies seeking regulatory compliance and pharmacovigilance support across clinical development and post-marketing stages. We specialize in helping biotechs navigate complex regulatory landscapes and manage drug safety, whether advancing through clinical trials, preparing for product launches, or expanding globally. | Insuvia is a trusted partner for biotech companies seeking regulatory compliance and pharmacovigilance support across clinical development and post-marketing stages. We specialize in helping biotechs navigate complex regulatory landscapes and manage drug safety, whether advancing through clinical trials, preparing for product launches, or expanding globally. Our tailored operating model is designed to meet the unique needs of biotech companies – offering agility, scalability, and personalized service. As a mid-sized provider, Insuvia combines the capacity to handle complex projects with the focused attention biotechs deserve. Backed by a highly experienced team, we enable our clients to achieve regulatory success and ensure patient safety.
Harvest Integrated Research Organization (HiRO)
HiRO is a modern global CRO delivering full-service clinical trial support across ANZ (for over 25 years), APAC, US, and Europe. We combine global infrastructure with genuine local expertise, offering sponsors the agility and personalization that larger organizations can’t match, without sacrificing rigor or reach. From regulatory strategy, clinical operation support and management, site identification and management, biometrics, pharmacovigilance and medical monitoring, HiRO accelerates the path from discovery to patients. Highlights ⦁ Modern local CRO operating across ANZ, APAC, US, and Europe ⦁ Full-service: clinical design, regulatory, biometrics, safety, and monitoring ⦁ Global expertise paired with hands-on regional insight ⦁ Agile operations built for faster, cleaner clinical data ⦁ True partnership model, embedded in your team from day one | Harvest Integrated Research Organization (HiRO) is a globally oriented, innovative clinical research organization (CRO). With global operations and integrated capabilities, HiRO provides a full range of cross-border solutions and services to its clients, including early pre-clinical strategic planning, clinical trial design, regulatory affairs, pharmacovigilance, statistics, data management, end-to-end project management, and clinical and medical monitoring services. As an emerging global CRO, HiRO strives to become a market-leading, integrated global clinical research organization that works collaboratively with biotech and pharmaceutical companies to bring new products from the laboratory to the market, providing more effective solutions for patients worldwide.
GlobalData
GlobalData has decades of experience in being the trusted, gold standard intelligence provider to leading Pharmaceutical brands, manufacturers, and suppliers, helping them to make faster, more informed decisions. | GlobalData is a data and analytics company providing the Life Science Community with Market and Competitive Intelligence. GlobalData serves over 4,000 world’s largest companies with over 600 healthcare analysts by gaining insights into competitors, evaluating market opportunities, and provide strategic opinions in the Pharma/Biotech, CMO/CDMO, CRO, Medical Device/Medtech and Consumer Health industries. From research and development, clinical trials, business developments to investment due diligence, our clients can make better business decisions on our fully integrated one-stop intelligence center platform. | GlobalData’s Construction portfolio offers insights across the entire global construction market, from market-sizing, companies, construction innovations, risks, regulatory developments, M&A, and financial transactions, to projects and project contacts. Our connected Construction Intelligence offers the most comprehensive coverage of construction projects available, tracking new construction projects totaling over US$70tn globally from announcement to completion, by sector, stage, scope, and more. Our industry leading portfolio of brands include Cranes Today, Tunnels & Tunnelling, and World Construction Network amongst others, and have informed the construction landscape since 1969.
GCCL
Accelerate your global trials with GCCL – All-in-One Clinical Lab Solution (Central Lab + BA Lab + R&D) GCCL, a Lab CRO based in South Korea, specializing in clinical sample analysis services for all phases of trials. With an exclusive lab service available for clinical trials and a logistics system that meets global quality standards, GCCL is building trust with over 200 partners globally by providing a sample analysis and bioanalytical service spanning the entire cycle of clinical trials to meet customer demands. Based in Korea as a strategic hub for the Asia-Pacific region, GCCL is South Korea’s only provider of a fully integrated “all-in-one lab solution,” combining a Central Lab, Bioanalytical Lab, and Biosafety Level 3/2 (BL3) facilities. This unified approach delivers consistent analytical quality, reliable data, and reduced time and costs by minimizing sample handling. Leveraging its proprietary G-HUB IT platform, cutting-edge analytical technologies, and global LIMS, GCCL provides end-to-end, high-quality clinical sample analysis services—from collection to storage—positioning itself as a trusted partner in drug development. Its dedicated R&D lab drives method development, biomarker discovery, and the evaluation of innovative analytical technologies, continuously enhancing capabilities to meet evolving clinical trial needs. -Supporting clinical trials with comprehensive laboratory services across all therapeutic areas and pipelines (from sample collection and kit production to analysis and storage) -Collaborating on R&D for pipelines, including biosimilars, bioanalysis, assays, and more -Offering clinical trial consulting, including study design and regulatory/approval support
FGK Clinical Research GmbH
FGK provides full service for clinical studies to biotechnology, medical device and pharmaceutical companies. FGK has the right size to handle international multi-center studies with hundreds of patients or single country studies with a few patients, but is still small enough to guarantee a personal service to the sponsor. With our more than 200 highly qualified medical, scientific and regulatory experts, we have all knowledge and experience necessary to succeed in Europe and can guide you through the clinical trial process, from planning and approval to the final report. Full service or partial services for conduct of clinical trials including: * clinical trial management and clinical monitoring * regulatory submissions * biostatistics * data management * eSolutions * medical writing * medical safety * quality assurance * pharmacovigilance * consulting services FGK also offers legal representation services for sponsor companies conducting trials in the EU without having a subsidiary there. | FGK is a European, owner-managed Clinical Research Organization providing full service for clinical studies to biotechnology, medical device and pharmaceutical companies. FGK has the right size to handle international multi-center studies with hundreds of patients or single country studies with a few patients, but is still small enough to guarantee a personal service to the sponsor. With our 240 highly qualified medical, scientific and regulatory experts in the EU and the UK, we have all knowledge and experience necessary to succeed in Europe and can guide you through the clinical trial process, from planning and approval to the final report. Full service or partial services for conduct of clinical trials including: ▷ clinical trial management and clinical monitoring ▷ regulatory submissions ▷ biostatistics ▷ data management ▷ eSolutions ▷ medical writing ▷ medical safety ▷ quality assurance ▷ pharmacovigilance ▷ consulting services; — FGK also offers legal representation services for sponsor companies conducting trials in the EU without having a subsidiary there (www.fgk-rs.com) and post-market pharmacovigilance services (www.fgk-pv.com).— | FGK Clinical Research GmbH is a full service Contract Research Organization with offices in Germany (HQ), Poland, Czech Republic, Hungary, UK and US. We provide full service for Phase I – IV clinical studies. Our international client base includes biotechnology, medical device, and pharmaceutical companies. FGK has the right size to handle multi-country, multi-center studies with hundreds of patients or single country studies with a few patients, but is still small enough to guarantee a personal service to the sponsor. With our about 240+ highly qualified medical, scientific and regulatory experts, we have all the knowledge and experience necessary to succeed and can guide you through the clinical trial process, from planning and approval to the final report. | FGK is a CRO, offering full service for conduct of clinical trials in all phases, specialized on biotech and medical device companies. Founded in 2002, owner-managed structure, guaranteeing a personal and flexible approach to our clients. FGK has the right size to handle international multi-center studies with hundreds of patients or single country studies with a few patients but is still small enough to guarantee a personal service to the sponsor. With our 240 highly qualified medical, scientific and regulatory experts, we have all knowledge and experience necessary to succeed in Europe and can guide you through the clinical trial process, from planning and approval to the final report. Full service or partial services for conduct of clinical trials including: * clinical trial management and clinical monitoring * regulatory submissions * biostatistics * data management * eSolutions * medical writing * medical safety * quality assurance * pharmacovigilance * consulting services
EPS Group
From our beginnings in 1991 as a systems company built on medical statistics, the EPS Group has responded to customer needs amid structural changes in the market and increasingly rigorous and complex drug development. EPS has evolved as a CRO (Contract Research Organization) and expanded our offerings to include SMO (Site Management Organization) and CSO (Contract Sales Organization) services, thereby becoming a comprehensive provider of various support services for the healthcare industry. CRO： In response to requests from pharmaceutical, medical device and regenerative medicine companies, medical institutions, governmental agencies, and others, the EPS CRO Group provides One-Stop Solutions to support the development of pharmaceuticals, medical devices, foods, and cosmetics. SMO： The EPS SMO Group enhances clinical trials by collaboration with medical institutions across Japan, leveraging digital technology to improve efficiency, including the promotion of Decentralized Clinical Trials (DCTs) and the development of remote systems for clinical trial document management. CSO： The EPS CSO provides targeted support to pharmaceutical and medical device manufacturers after product approval. We provide contact center operations, and a range of services from pre-approval to post-marketing stages, employing a skilled workforce to effectively fulfill customer needs. | EPS Holdings, Inc., a Japanese headquartered company, is a comprehensive provider of clinical trial and research outsourced services. EPS Group, with over 7,800 staff, provides quality support to pharmaceutical, biotech, regenerative medicine, and medical device companies. Core businesses are CRO, SMO, Contract Sales Support, and China product development and distribution. EPS operates in Japan, China, South Korea, and Taiwan and, through a partner, supports studies in other Asia-Pacific countries. Looking towards the future, we will strengthen our forward-looking spirit expressed as an “Ever Progressing System.” | The EPS Group was founded in 1991 as a pioneer in the domestic Contract Research Organization (CRO) industry. Since then, we have expanded our diverse services, including Site Management Organization (SMO) and Contract Sales Organization (CSO), with a primary focus on CRO. We provide end-to-end support solutions from the development of pharmaceuticals, medical devices, and regenerative medicine products to post-marketing surveillance. Building on the foundation of our clinical trial and post-marketing businesses, which boast a top-tier scale and proven track record in Japan, we are actively engaging in data business and new ventures, constantly striving for evolution.
EFOR Group
Founded in 2013, Efor Group is a leading international player in quality and compliance for the Life Sciences industry. With over 3,000 employees across 18 countries, Efor supports leading pharmaceutical, biotech, and medtech companies in securing their manufacturing operations through its expertise in CQV, quality management, and regulatory compliance, while accelerating the delivery of innovative therapies to market. Our mission: to remove technical and regulatory barriers, enabling faster access to innovation while ensuring the highest standards of safety and reliability. Committed to its founding values, Efor fully integrates social and environmental responsibility into its business model and drives sustainable growth built on excellence, commitment, and teamwork. Through its international expansion, the Group aims to establish itself as a global reference in Life Sciences consulting, placing people, health, and safety at the heart of everything it does.