E-Volunteer’s full-service products give drug development programmes a straightforward, complete solution. We provide the highest standards of service, integrity, dependability, and quality under the direction of a senior management team with experience in pharmacology, pharmacokinetics, bioanalysis, statistical analysis, clinical operations, medical affairs, and project management.
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Clinical research services (Phase I to IV and BA/BE studies), medical writing (scientific and regulatory writing), clinical data management, and regulatory affairs are provided by Bio-clinical Research to the global bio-pharma business.
e-Volunteer. provides services for Method Development, Method Validation, and Analysis of Study Samples to the global pharmaceutical sector.
Biostatistics and Pharmacokinetics (PB). You will receive technical help from a committed and skilled staff of biostatisticians throughout the whole clinical development process. From pre-clinical analysis to clinical and post-marketing services across diverse therapeutic areas, our staff has experience in all stages of research and development. We provide cost-effective, high-quality complaint services. All PB processes are carried out in accordance with clear SOPs, checklists, and documentation, and they all adhere to ICH standards and regulatory requirements.
Our strategy is to focus on quality.
collaborating with outstanding individuals to provide top-tier services
Commitments will be closely watched and kept.
World-class infrastructure that is affordable
Our guiding principle is transparency with rigorous adherence to international laws.
We maintain the highest standards.