Our Services
Well-prepared data is crucial for regulatory submission success. A data-focused CRO like Quanticate offers expertise in data capture, analysis, and reporting. Trust your study’s data to clinical data experts from start to finish.
BIOSTATISTICS
Understand your drug’s/device’s efficacy and safety profile with expert statistical analysis of your clinical research data.
STATISTICAL PROGRAMMING
Turn un-interpretable validated clinical data into something meaningful with clinical trial reporting to make informed decisions and submission ready deliverables.
CLINICAL DATA MANAGEMENT
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.
STATISTICAL CONSULTANCY
Ensure efficient trial designs, analysis and study planning to streamline your clinical development efforts to reduce costs and save time.
MEDICAL WRITING
Give your regulatory submission the best chance for approval with well written regulatory documents throughout all stages of the drug development process.
REGULATORY SUBMISSION REVIEW
Ensure that your regulatory submission isn’t needlessly delayed through a lack of quality or integrity of data.
PHARMACOVIGILANCE
Quanticate offers a fully compliant and high-quality complete package of pharmacovigilance services.
PK/PD ANALYSIS
Discover what the body does to your investigational drug and where it goes with PK and PD analysis.
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Address
360 E. 1st Street #4139, Tustin, CA 92780
Email Us
BD@avansightinc.com