• We can provide the following services for customerProduct testing Draw up technical requirements documents Assist medical device enterprise to consult face-to-face CDE statistical review expertsGenerate registration strategy (For example: To evaluate whether this product can be exempted the clinical trail)Complete and submit registration data Follow up and answer one-time supplementAssist the on-site inspection Get the license 

  • We can provide the following services for customerProduct testing Draw up technical requirements documents Assist medical device enterprise to consult face-to-face CDE statistical review expertsGenerate registration strategy (For example: To evaluate whether this product can be exempted the clinical trail)Complete and submit registration data Follow up and answer one-time supplementAssist the on-site inspection Get the license  Estimate project difficulty and control project risk in order to for purpose of successful registration 

  • Our service covers registration, clinical trail and post-marketing clinical trail of drug and medical device. Our company has taken over nearly hundred of clinical research projects since launch, most of which are international multicenter and registration clinical trials, and we have rich experience in more than twenty fields, such as respiration, digestion, tumour, incretion, cardiovascular, skin, nutrition. Our investigators covers 100% of clinical trail institutes, distributed in more than twenty provinces and direct-controlled municipalities across China, to provide convenient and high-quality project management and monitoring service for you.    ① Project management     - Formulate and implement project management plan and risk management plan    - Formulate and implement project budget control plan     - Assist customer to complete center screening, investigator selection and patient recruit at full speed    - Organization and convening routine investigator meeting     ② Monitoring     - During clinical monitoring, execute strictly SOP of customer or our company     - Inspection of Case Report Form, original data inspection, data question form solution and other monitoring related works     - Center screening, launch, convention and close visiting  - Assist researchers to provide serious adverse events reports and relevant documents to customer and government supervision department - Storage, distribution and check of research drugs  - Management and update of research documents 

  • Team members all have medical background, know various data management system well, are fluency in Chinese and English and use all kinds of data management system according to customer’s requirements. And provide high-quality and low-cost data management service. -Data management consultation -Data management manual/guideline -Project training -Database design and establishment -Data input and proofread -Data validation and question solution -Medical code -Data quality check -Data management report -Database lock and transferring -Data transmission of central laboratory-Filing 

  • Our statistical team has rich experience, senior background, and designs statistical project with moderate cost, good safety and great chance of success and statistical analysis report meeting the domestic and overseas newest clinical statistical standard according to product characteristics and benefits of sponsor. -Design of trail sample -Design and consultation of trail protocol and CRF (PhaseⅠ~Ⅳ)-Design random table & execute randomly -Make statistical analysis plan-SAS programming& program confirmation -Statistical analysis (Including interim analysis, terminal analysis and blind review)-Statistical report writing 

  • Service for clinical research quality inspection mainly includes the inspection to research centers and sponsor’s research documents. Our investigators all have more than ten years of working experiences related to clinical trail. Our company has taken over nearly hundred of clinical research projects since launch, most of which are international multicenter clinical trails. Our investigation standard is specified in ICH GCP and relevant regulations specified by the state, and the primary customers are global large-scale pharmaceutical enterprises ranked top 20. 

  • The medical team members are all engaged in medical supporting work, with MS/PHD and have served in domestic top three hospitals and in attending or above position. Up to now, the medical team has completed nearly 300 protocols and 200 clinical final reports involving in 22 fields totally. We have innovative and practicable SOP. Intervention at early of the project, and expert consultation, information retrieval, protocol writing and template are all done under regulations with great scientificity and strong normalization. So far, we have 60 experts to provide us consultation service, and fields involved including: cardiovascular, tumour, respiration, orthopedics, incretion, urinary, blood, digestion, rheumatism and immunology, paediatrics, gynaecology, ophthalmology and so on.  We can provide rather professional medical support meeting the market for you. 

  • Pfarrell provides project approval at early development, clinical development and execution and  post-marketing academic promotion one-stop adjective product development service by own product database and with the help of senior industry experts. And assist enterprise to complete project assignment, product developing market, find product appreciation space and other matters. 

Pfarrell (Shanghai) Medical Development Co, Ltd (herein after referred to as Pfarrell) is an advanced clinical CRO and pharmacy consultative agency in China. By supplying medical enterprises and research institutes with professional technical services like clinical research and registration, project appraisal, academic services, international registration, academic promotion outsourcing and R&D investment and financing management, etc, we help our cooperators accurately predict and efficiently reduce the investment risks of new products and market promotion, assist the incubation and listing of new technology as soon as possible and provide one-stop solutions to the internationalization of outstanding pharmaceutical enterprises in China.