Bring your drugs to market with fast and reliable access to expert teams
By choosing Quanticate as your specialist partner for biometric services for clinical trials, you can trust that your data will be in safe hands, from the design of a study through to final submission.
High quality and well-prepared data can make the difference in a successful regulatory submission or disappointing delayed approval. Whereas full-service CROs may see data as an afterthought, a niche biometric CRO such as Quanticate brings expertise and quality to data capture, statistical analysis, and clinical trial reporting.
Biostatistics
Understand your drug’s/device’s efficacy and safety profile with expert statistical analysis of your clinical research data.
Biostatistical Consultancy
Ensure efficient trial designs, analysis and study planning to streamline your clinical development efforts to reduce costs and save time.
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.
Medical Writing
Give your regulatory submission the best chance for approval with well written regulatory documents throughout all stages of the drug development process.
Pharmacovigilance
Quanticate offers a fully compliant and high-quality complete package of pharmacovigilance services.
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