We provide the full suite of biometrics services, including clinical data management, biostatistics and statistical programming to successfully execute your study.
Explore our areas of expertise, ranging from clinical operation, medical affairs, data management, pharmacovigilance, and local sponsor representatives for international companies.
Our Biostatisticians are engaged through the life of the project from study design to finalisation of the clinical study report (CSR). Our group will provide high-quality tailored solutions to ensure successful completion of your study.
Our Clinical Data Management Team will ensure all data collected within pivotal phase clinical trials are optimally powered and suitable for all major regulatory authorities around the globe, including the Federal Drug Administration (FDA).
Our Statistical Programmers have a vast range of experience producing table listings and figures (TLFs) for various therapeutic areas, study designs and phases. Our team will ensure all requirements for electronic data submissions to regulatory authorities are successfully met for your study.
Our Biometrics Team will carefully analyze bioavailability and characterize a drug’s absorption, distribution, metabolism and excretion (ADME) properties to enable effective clinical studies. We will provide detailed recommendations around dosage, drug interactions in the body, and patient diversity.
Complete Phase CRO is dedicated to helping small to medium size biotechnology and pharmaceutical companies worldwide advancing their innovative products and breakthrough science in to new medical treatment.
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