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At ACL Digital Life Sciences, our clinical data managers are well-experienced in hosting EDCs or providing vendor oversight. Our clinical data managers have years of experience in multiple therapeutic areas across all Phase I-IV studies. We are highly qualified in CDISC compliance and SME-level expertise to produce results with the speed and accuracy you need. Clinical data management supports the conduct, management, and analysis of studies throughout the entire period of clinical research. CDM comprises legacy paper and contemporary electronic case report form designing, clinical trials database design and programming, data standards implementation, data acquisition, data integration into the clinical trials database, data review, validation, coding, and database finalization.

Our clinical expertise includes establishing and maintaining good clinical practice compliance programs for all phases of drug development. We also have broad experience with GCP compliance audits of clinical sites, clinical laboratories, drug safety databases, data management centers, and contract research organizations.

You can count on our scientific-minded and experienced writing team to prepare clinical documents for regulatory authorities, including protocols, clinical study reports (CSRs), and DSURs. From authorship planning to publication selection stages, you can depend on our experts to bring your device or new medicine from concept to market. ACL Digital Life Science's medical writing team meticulously plan and prepare the publications after an in-depth assessment of qualitative and quantitative gaps that ensure value-based content at every stage. Our medical writing teams support multiple therapeutic areas.