our services
Our Services
Max Clinical is fully equipped to offer a wide range of Clinical Research Services to its clients. We comply with GCP, GLP and other applicable regulatory and statutory requirements to meet the criteria of Quality, Data Integrity, Safety and Ethics.
The array of our service capabilities include:
SMO - Site Management Organisation
- Project Management
- Site Management
- Clinical Trial (Phase I-IV)
- Early Phase Studies (BA/BE,PK/PD)
Medical Writing
- Manuscript
- CSR (Clinical Study Report)
- Protocol Development
CDM
- Clinical Data Management
Statistical-Analysis
Bio Analysis
Pharmacokinetics & Pharmacodynamics
Bio-Statistical Analysis
Straight from our clients
Max Clinical Research Solutions provided exceptional support and expertise during our clinical trial process. Highly recommended!
Kumar
Their professionalism and commitment to quality made our clinical trials efficient and successful. Truly impressive service!
Deepika
Max Clinical Research Solutions delivered outstanding support throughout our clinical trial process. We highly recommend them.
Mahesh