Services

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.

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PSUR / PBRER

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.

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CLINICAL TRAILS

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.

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MEDICAL INFORMATICS

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.

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BIOSTATISTICS

Understand your drug's/device's efficacy and safety profile with expert statistical analysis of your clinical research data.

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MEDICAL WRITING

Give your regulatory submission the best chance for approval with well written regulatory documents throughout all stages of the drug development process.

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PHARMACOVIGILANCE

Edriza offers a fully compliant and high-quality complete package of pharmacovigilance services.

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