THERAPEUTIC EXPERTISE
Developing new drugs to treat human disease is an expensive, complex and time-consuming process. Bringing a new drug to market can take up to 15 years and costs $2.5 billion or more.
Our biopharmaceutical and biotech customers have trusted us to help them advance their trials. Our therapeutic area expertise spans large drug disease markets such as hematology/oncology and chronic conditions along with growing areas of R&D innovation, such as immuno-oncology, cell and gene therapy, biomarkers and rare diseases.
At every stage of the drug development process, PPD deploys the expertise you need to design, plan and execute your clinical trials with skill, precision and unwavering focus on quality.
LEARN MORE ABOUT WHAT WE DO
Clinical Trials >
Our commitment to ethical research, patient safety, and scientific excellence sets us apart as a leading provider of clinical trials services.
Phase II-IV >
Shen Clinical Services has the capability to conduct trials across all phases, from initial safety assessments to large-scale efficacy studies
Clinical Trial Management >
We encompassing design, site selection, patient recruitment adhering to all the regulatory compliance.
Data Management and Biostatistics >
We ensures precise data management and analysis, vital for meaningful clinical trial results.
Regulatory Submissions >
Shen Clinical Services oversee safety data, report adverse events, and conduct pharmacovigilance to ensure patient well-being and regulatory adherence
Pharmacovigilance >
Shen Clinical Services oversee safety data, report adverse events, and conduct pharmacovigilance to ensure patient well-being and regulatory adherence
Quality Assurance >
Shen Clinical Services maintains strict quality standards for regulatory compliance, ensuring excellence in processes and documentation
Medical Writing >
Skilled medical writers assist in the preparation of clinical trial documents, including protocols, informed consent forms, and regulatory submissions