Clinvigilant supports biotech, pharmaceutical and medical device companies with tailored clinical Operation Services. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver. With Clinvigilant you get a shared commitment to your success.
Clinvigilant Research provides skilled project managers that are well suited to the needs of clinical trials. With an average tenure of 10+ years in the industry..
EDC & Data Management
Our databases fulfill important baseline attributes while allowing for the specialized configuration required for regulatory report outputs, and are configured with..
Clinvigilant Research monitors have experience with both outpatient and inpatient records and procedure notes. Monitors are also trained in control response reduction..
Pre-Post Regulatory Support
ClinVigilant provides inclusive regulatory operation services to Pharmaceuticals (FP and API), Biopharmaceutical, and Healthcare, CMO and Clinical Research industry..
Clinvigilant Research medical writers are experienced in both clinical and regulatory writing techniques to provide concisely written documents that exceed client expectations..
Quality Assurance & Auditing
As a part of quality assurance activities, we improve the reliability of clinical studies, post-marketing clinical studies, clinical research etc. by evaluating and verifying compliance..
Computer System Validation
Many regulated companies, such as those in life sciences, food and beverage, and the cosmetics industry, worry about time and resources required for software validation..
CRO Set up
We can help you to setup/establish new BE centre /CRO/ bioanalytical lab/clinical facility. We have decades of experience in BE centre setup. We can give end to end BE centre setup support..