Optimize every aspect of your biometrics requirements, from study design to data management, analysis and submission
Our comprehensive end to end biometrics solution provides high-quality support across every stage of your clinical development, so you achieve: robust results, timely progress, and regulatory readiness. Every time.
We shape our support to fit your exact needs. From fully outsourced data management, reporting and large submission deliveries to embedded consultancy for tasks such as Study Data Tabulation Model (SDTM) conversion or CDISC standards implementation.
Our global team brings expertise in a variety of EDC platforms, SAS and R programming across multiple reporting environments, client systems, and therapeutic areas. Trained through the Veramed Excellence Program, our programmers combine technical skill with consultancy and customer-focused support.
We have a 90%+ retention rate. With dedicated global teams, we offer continuity and consistency across every project, no matter where you’re based. As a certified B Corp, we foster a strong company culture with teams that care and have the time to focus on your project’s success.
We’re a proud member of the Clinical Data Interchange Standards Consortium (CDISC) and a recognized leader in industry initiatives, actively shaping the future through data set JSON, and by leading panels at PHUSE, PSI, ACDM, and SCDM.
Accelerate Study Success: Automate Workflows, Future-Proof Results, and Streamline Delivery
Accelerate Study Success: Automate Workflows, Future-Proof Results, and Streamline Delivery
Accelerate Study Success: Automate Workflows, Future-Proof Results, and Streamline Delivery
Accelerate Study Success: Automate Workflows, Future-Proof Results, and Streamline Delivery
Accelerate Study Success: Automate Workflows, Future-Proof Results, and Streamline Delivery
Accelerate Study Success: Automate Workflows, Future-Proof Results, and Streamline Delivery
End-to-end biometrics services cover the full lifecycle of clinical trial data, from study design and data management to statistical analysis, reporting, and regulatory submission. These services ensure high-quality, compliant, and efficient trial delivery.
Veramed sets a new standard in biometrics: combining expert teams, cutting-edge tech, and a culture of care to deliver data you can trust. Our services go beyond the CRO playbook, offering tailored, audit-ready solutions that drive confident decisions. As a Certified B Corp, we’re committed to doing good work, fast and right the first time: no rescues, no surprises, just biometrics built better.
Veramed’s biometrics teams can support you at every stage of your trial, including protocol review, randomization, interim analyses, DMC/DSMB support, CDISC standards implementation, statistical reporting, regulatory submission, and publication planning.
Yes, Veramed is a proud member of CDISC and provides full CDISC-compliant services including SDTM conversion, ADaM implementation, Define-XML, SDRG, ADRG, and gap analysis to ensure submission readiness and regulatory compliance.
Veramed uses a robust quality control process that includes expert statistical review, thorough checks, and consistent team support across global locations to ensure every output is accurate and submission-ready.
Absolutely. Veramed supports ISS/ISE development, CSR input and review, data anonymization, and complete CDISC documentation to meet transparency and privacy standards for global regulatory submissions.
While our expertise spans a diverse spectrum of therapeutic areas, our principal focus lies in supporting trials in oncology, respiratory, rare diseases, and ophthalmology, where our teams have delivered transformative results for clients worldwide.
