Our Services
SPDM Clinical Research helps pharmaceutical companies, medical device and biotech companies move from clinical trial research through clinical trial submissions. We offer full services in various therapeutic areas for various milestones including study design, study size and scope, we provide customized CRO services and solutions that produce quality data suitable for various regulatory agency submission.
We have over 60 years of accumulated experience in helping small to big pharmaceutical companies to improve CTMS, clinical trial processes, resources management and achieve compliance. Working with us can decrease costs, improve efficiency, data quality and assure data integrity for every trial for the clinical trial submissions.
Clinical Trial Study Design
Our team investigates, designs, delivers appropriate clinical trial designs and perform sample size calculations.
CTMS Services
Our team designs and delivers clinical Trial Management Systems (CTMS).
EDC Services
Our team sets up clinical monitoring, EDC systems, Data Management services including ETL
Database Development
Our team designs, deliver database solutions and electronic CRF specifically for your study.
Statistical Services
Our team performs statistical analysis and reporting based on protocol-specified endpoints.
Submission Services
Our team provides you the support not only in the creation of e submission packages but also compiles all types of eCTD submissions and eCDT lifecycles, Regulatory submission documents, correspondence and submission archives.
-- Let us know how we can help improve the quality and performance with your next clinical trial.