PHDS HEALTHCARE RESEARCH Co., Ltd.
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Global standards and quality systems, one-stop drug discovery and preclinical research services and solutions.
Clinical Research
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Phase II-III clinical trials
One-stop II-III phase clinical research solutions
Precise positioning, professional executionPHDS CRO is dedicated to providing comprehensive II-III phase clinical research solutions. From preliminary assessment to confirmation stage, we ensure that every step is precise and efficient to meet your drug development needs.
Phase II clinical research: Concept validation and dose optimization
Target precision:Our Phase II services focus on the preliminary assessment of drug efficacy and safety, laying a solid foundation for Phase III research.
Scale customization:We precisely control the number of subjects between 100-300 based on project needs, ensuring the reliability and statistical significance of the data.
Design diversification:Employing various designs such as randomized blind controlled trials, including concept proof in Phase IIa and dose finding in Phase IIb, to adapt to different research objectives.
Phase III clinical research: Efficacy confirmation and risk assessment
Scale expansion:In Phase III, we expand to 1000-3000 subjects to obtain results with greater statistical power.
Design rigor:Conducting randomized, controlled, multi-center trials to ensure the scientific validity and reliability of research results.
Result authority:Phase III research results directly support drug registration applications, providing key evidence for drug market approval.
One-stop service, comprehensive coverage
PHDS's one-stop service includes but is not limited to:
1. Compliance assurance: Strictly adhering to GCP and SOP standards to ensure research compliance.
2. Project management: From clinical site selection to multi-center trial management, we provide comprehensive project management services.
3. Protocol writing and drug management: Professionally writing clinical trial protocols and accurately conducting drug blinding distribution.
4. Subject recruitment and management: Efficiently recruiting suitable subjects to ensure the smooth progress of trials.
5. Monitoring and data analysis: Providing clinical service monitoring to ensure data accuracy and completeness.
6. Application document writing: Professionally writing clinical application documents to accelerate the drug approval process.
Choose PHDS, accelerate drug market entry
We understand the complexities and challenges in the drug development process. PHDS CRO's one-stop solution aims to simplify processes, improve efficiency, and ensure that your project can quickly and smoothly transition from the laboratory to the market. Choosing us means choosing a trusted partner; we will work hand in hand with you to drive the success of drug research and development.
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Contact Information
Customer service hotline:
E-mail:customer@cnphds.com
Address: Building A, Ocean Express,66 Xia Guang Li, Dong San Huan North Road,Chaoyang district, Beijing, China
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