Our Clinical Trial Solutions
Clinical development is dynamic, multifaceted and challenging. It involves skilled manpower investing thousands of hours with zeal for research and innovation in drug discovery. This long process involves collaborating and developing long term partnerships that are part of the success story. We at Clinvigilant help you reach your clinical development objectives from Phase II to Phase IV clinical studies across different therapeutic areas. From exploratory studies, to confirmatory and post approval studies, we can address all your needs effectively and efficiently with optimized resources. Our team consists of well trained and experienced clinical research professionals with skill sets in medical writing, clinical trial monitoring, biostatistics, pharmacovigilance and regulatory support.
Our Digital Clinical Trial Platform
We provide study specific digital solutions to conduct studies remotely from any part of the world. All our systems are secure and maintain data integrity and protection.
We collaborate with sites globally and have access to numerous medical institutes throughout different part of the world"
We have been audited by EMEA, MHRA, FDA and DCGI
Electronic Data Capture (EDC)
Electronic Trial Master File (eTMF)
Patient Engagement
Bringing it all together to enhance the patient experience
Data Management
Regulatory Submission
Regulatory Inspection
Satisfied Customers
Do you have a Clinical Site?
Interested in learning more about how to participate in a clinical trial?
Our Offices
United KingdomIndia
Email Address
bd@clinvigilant.comBusiness Enquiry
+44 1322 643254+91 99130 11134
Careers
Send your resume tohr@clinvigilant.com