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The biostatistics team at Panacro is dedicated to providing a full range of statistics-related professional services from study design to submission of study results.
Generally, the biostatistics team is usually involved from the planning stage of a clinical study, playing a crucial role in the entire project, from clinical trial design, sample size estimation to protocol writing and review.
It will develop and execute the analysis plan on time to ensure high-quality analysis results during the clinical trial.
Experienced in communicating with food and drug regulatory agencies, ethics committees and investigators, Panacro statisticians are capable of making effective communications on behalf of customers.
As a high-quality technical team with rich experience in international and domestic clinical trials, the team specializes in management of clinical trials, post-marketing and key testing items and safety data.
By strictly following NMPA data management regulations and combing with years of hands-on experience in international project operation and corresponding quality standards, the team has undertaken hundreds of clinical trial projects of various phases mainly in oncology, psychoneurology, autoimmunity, etc. and has been widely recognized by the industry.