Using technology and expertise to streamline clinical trials
Inspired by science and quality, Clinvigilant was established in between the UK and India as an efficient as well as convenient one-stop solution for clinical trials from phase I-IV.
We rely on technology and matter experts as a mean to streamline clinical trial processes to increase performance, reduce errors and cut redundant activities without making it cost you a fortune. Let´s democratize efficiency.
Clinvigilant three main business lines are: eClinical solutions, CRO services and Consulting services for Pharmaceuticals, Biotech, and any clinical research company/institution such as universities or trusts.
Our Approach
ClinVigilant approaches every client’s business as if it were our own. We believe a consulting firm should be more than an advisor. We put ourselves in our clients’ shoes, align our incentives with their objectives, and make it easier for them to run clinical trials.
The right approach is necessary for the right outcome. ClinVigilant approaches work by applying its extensive knowledge to your organisation’s SOW. We know that in order to maximize the potential of success for your company we need to shape our expert advice in a way that applies to your way of doing things.
Zero Tolerance on Quality
Timely
Deliverables
Ethical
Practice
Cost-Effective
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