Clinical Statistical Analysis Consulting
Osmunda Medical Device Consulting Organization (Guangzhou, Shanghai, Suzhou, Shenzhen, America) is a professional consulting company, who focus on medical device laws and regulations consulting, medical registration, quality system and product certifications consulting. We are becoming the largest the mightiest consulting organization in the field of Medical Device in China. Some of our clients include Biomet, Tyco, GE, Philips, Sumitomo, Vtech, Bio Medical, Kewei, Shenzhen Saycold, Japan Gunzesz and ONBO, etc.
Clinical trial is an initial but the most popular way combining medicine with industry. It‘s viewed as essential for new-type medical device product to be socially
accepted, before which, the product should be detected for index of physicochemistry and biology and safety by the third party.
In analysis of clinical trial data, statistic model should be selected based on objective, design plan and type of data, and whether parametric or nonparametric statistics should be applied depend on principle of statistics. Three objectives of statistic analysis of clinical trial include quality control, safety monitoring and writing report after the trial.
Statistic analysis plays an important role in design, supervision, mid-term analysis, terminal analysis and report of clinical trial.
Osmunda Medical Device Consulting Organization, based on regulation of related department on clinical trial of medical device product, selects our clinical medical institutions to perform clinical trial for your product, assist the institutions to make clinical schemes and follow up the clinical trial result to finish report efficiently with high quality. We will deliver our best consultants and best quality service to you to achieve your goals.