Professional, High-Quality Medical Affairs Services
Supporting the entire lifecycle of clinical research, ensuring scientific validity, safety, and feasibility.
The medical monitoring team is composed of highly educated talents with clinical medicine, clinical pharmacology and other backgrounds, more than 90% have clinician background, 20% have medical doctor degree.
For domestic and foreign pharmaceutical enterprises, innovative drug research and development companies to provide professional and efficient medical supervision services, has accumulated nearly a thousand clinical project medical supervision experience, involving cancer, respiratory, immune, nervous, infection, endocrine, gynecological reproduction, five senses and other diseases.
Our Strengths
Comprehensive Medical Monitoring Services
- Clinical protocol development
- Inclusion/exclusion criteria verification
- Review of protocol deviations (PD) with professional medical advice and solutions
- Full medical support for clinical research teams
- Regular medical review of clinical data, adverse events (AEs), and other incidents
- Inclusion/exclusion criteria verification
- Review of protocol deviations (PD) with professional medical advice and solutions
- Full medical support for clinical research teams
- Regular medical review of clinical data, adverse events (AEs), and other incidents
Professional Clinical Medical Knowledge
Our CRAs have clinical practice experience and research expertise. Staff members includes chief physicians, associate chief physicians and attending physicians who are familiar with diagnosis and treatment in various therapeutic areas, providing efficient and professional medical support during clinical research.
Efficient Data Review
We closely monitor global regulatory trends and clinical guidelines to ensure the scientific, reliable, and complete nature of clinical trial data. By conducting accurate trend analysis on research data, we ensure the smooth progression of clinical studies.
Learn how our medical strategy services, tailored to your market and product characteristics, can help accelerate your clinical trial process and regulatory submissions.
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