In the complex process of clinical trials, medical support supporting services play a vital role. They can not only ensure the medical science and ethics of the trial, but also provide the sponsor with comprehensive medical consultation and support to reduce trial risks and Improve test quality. At the same time, medical support supporting services can also provide better medical protection for subjects to ensure that their rights and safety are protected. Medical support supporting services provide comprehensive medical and scientific research support for the entire clinical trial process. Our medical support supporting services are committed to providing customers with professional, comprehensive and efficient medical services to ensure the smooth progress of clinical trials.
**1. Service Overview**
Medical support supporting services cover multiple aspects of clinical trials, including medical plan design, medical supervision, and medical data review and analysis. We have a professional medical team with profound medical background and rich clinical experience, able to provide customers with comprehensive medical support and guidance.
**2. Service content**
1. **Medical plan design**:
- Assist clients in formulating medical plans for clinical trials, including trial design, sample size estimation, inclusion and exclusion criteria, endpoint indicators, etc.
- Provide professional medical advice and guidance based on customer needs and research objectives to ensure the scientificity and feasibility of the plan.
- Assist clients to communicate with the ethics committee to ensure that the trial plan complies with ethical principles and regulatory requirements, and protects the rights and safety of subjects
2. **Medical Surveillance**:
- Dispatch experienced medical monitors to conduct regular or irregular monitoring of clinical trials to ensure that the trial process complies with medical ethics and regulatory requirements.
- Timely discover and solve medical problems that arise during the trial to ensure the safety and rights of subjects.
- Provide researchers with medical consultation and support during the trial to ensure the smooth conduct of the trial.
- Make medical evaluation recommendations and treatment recommendations for adverse events that occur during the trial.
3. **Medical data review and analysis**:
- Responsible for the medical review of clinical trial data to ensure the accuracy and reliability of the data.
- Conduct professional medical analysis of trial data to provide effective data interpretation and result prediction.
- Assist clients in writing clinical trial summary reports and medical papers, and provide high-quality medical support.
4. **Medical Consultation and Training**:
- Provide professional medical consulting services to customers and answer the medical problems encountered by customers during clinical trials.
- Assist clients to communicate with regulatory agencies and submit necessary medical documents.
- Regularly organize medical training activities to improve the clinical trial capabilities and medical literacy of the client team.
**3. Service advantages**
1. **Professional Team**: We have a professional medical team whose members have profound medical background and rich clinical experience, and can provide customers with high-quality medical support.
2. **Rich experience**: We have accumulated rich experience in clinical trials and can provide customers with scientific and feasible medical plan design and monitoring suggestions.
3. **Efficient Service**: We adopt advanced management methods and tools to ensure the timeliness and efficiency of medical support services.
4. **Comprehensive Support**: We provide a full range of medical support services, from protocol design to data analysis, to ensure the smooth progress of clinical trials.