Looking for additional support on your investigational drug
or device development?
Bring your drugs to market with fast and reliable access to
expert teams with our data focused CRO services for clinical trials.
Edriza consultants and staff have 12 years of experience of planning and writing periodic safety update reports, PADERs and DSURs in a cost-effective way. Whether it is a single simple DSUR or PADER or complex PSURs, we can meet the need.
Flexible and modern data collection, capture and management methods for your research data to ensure error free and timely database locks in line with the latest regulatory guidance.
Medical informatics is the study and application of methods to improve the management of patient data, clinical knowledge, population data, and other information relevant to patient care and community health.
Understand your drug's/device's efficacy and safety profile with expert statistical analysis of your clinical research data.
Give your regulatory submission the best chance for approval with well written regulatory documents throughout all stages of the drug development process.
Edriza offers a fully compliant and high-quality complete package of pharmacovigilance services.