Connected-Pathology

Across four decades, Propath’s GLP and GCP compliant facility in the UK has successfully collaborated on studies with biopharmaceutical companies, large and small, across the world. Today we are recognised as a leading specialist in spatial biology, molecular pathology and histopathology, collaborating with clients across the globe to advance their clinical and pre-clinical programmes. The quality of our service is rooted in the expertise and professionalism of our brilliant scientists and technicians – who bring a rich blend of insight, thoroughness and experience to every study we undertake – from routine histology and immunohistochemistry to advanced spatial transcriptomics and ultra-high plex IHC. And our vision to keep investing for the future – in our people and our technology – will ensure we continue to provide a service that is as responsive, innovative and dependable as our clients require. We are specialists in molecular pathology and histopathology for biopharma R&D. The award reflects the collective efforts over many years of our highly committed scientists and technicians, working collaboratively to support our clients’ research. Trusted by our clients – small and large – across the world. We believe the details matter: offering genuine expertise, ensuring robust Quality Assurance and being precise in our work.

We are actively involved in technology-based research covering pioneering new tissue processing techniques and digital pathology in diagnosis. We are continually recruiting sessional pathologists to cover our expanding work profile. We deliver a complete range of histology services with rapid turnaround times directly from our own CQC registered and ISO 15189:2012 accredited laboratory. We are committed to investing in and developing our people to the highest possible standard; as evident by obtaining IBMS approved training laboratory status. Our client training program along with dedicated account management makes migrating from one service provider to CPS a seamless, timely and trouble-free process. With no long-term agreements, complex pricing or hidden charges, our service couldn’t be easier to use. From sample pickup to result, we deliver everything you require to utilise our service. In addition, we also provide access to our secure online portal to:.

We are focusing on clinical applications and clients from pharmaceuticals, diagnostics biopharma, biotech, contract research organisations (CROs), biobanks, and other players. Our services are organized under four business lines: Central Lab Services, Site Management Organization, Precision Medicine and Companion Diagnostics. We provide end-to-end services including biomarker discovery, target validation, CDx assay development, commercialization, and regulatory services. We continually monitor our service and operations to assure that the highest level of compliance and quality is maintained. We are dynamically growing, expanding our worldwide capabilisties. We are committed to fostering a globally diverse workforce and a companywide culture that encourages excellence, leadership, innovation and a balance between our personal and professional lives. We provide comprehensive clinical services, study execution and consulting services covering a wide range of therapeutic fields, such as oncology, immunology, CNS, vaccines, rare diseases, and more. We offer comprehensive clinical research one-stop-shop solution for Pharma, Biotech and CRO companies.

THE SCIENCE-DRIVEN BIOPARK AT THE HEART OF EUROPE. We provide services throughout a company's life from inception. State-of-the-art technology platforms with cutting-edge expertise for experiment design and execution to support therapeutics development projects.

Our services provide data insight to study sponsors, researchers and investigators in the quest of changing lives by improving medical outcomes thru innovative new drugs, therapies and biologics. The foundation of our service is to ensure and promote subject safety, protocol integrity and actionable data in the development of clinical research trials. We are the only 21 CFR part 11 fully compliant local and central laboratory not affiliated to a CRO in the United States (USA). Established in 2022, our laboratory has become a global leader in clinical laboratory data. Our state-of-the-art laboratory features the latest advances in laboratory innovation and automation. Our GCP ICH E6 compliant services provides fast, accurate and reliable data to ensure standardization and subject safety. One Pharma Lab is a CLIA certified CAP accredited laboratory. We specialize in servicing research sites, principal investigators and study sponsors.

To help you change the world for the better. We believe you can do it and we know we can help. Our deep commitment to your success stands on these four pillars:. We do this and do it well by forging two paths that converge. We provide a full-service solution for clients needing both a CAP/CLIA Diagnostics and Contract Research facility. Our highly-skilled and patient-focused Clinical Diagnostics team provides clinical laboratory testing in our CAP/CLIA-accredited facility.