Vigilare is an emerging biopharmaceutical consulting company providing integrated offerings and outsourced support in Pharmacovigilance and Drug safety, Clinical trials, Medical writing, Clinical data management, Regulatory affairs, BA/BE studies, Medical and Scientific consultation and US agent services.
We deliver our services for the globally renowned Pharmaceutical Industries, Generic Players, Biotechnology firms, Biologics and Medical Device industries.
Our peerless zeal towards continuous development and excellence is a motivating factor to meet and exceed the expectations of our clients.
Due to our US and international industry experience, we are well suited to provide your Pharmacovigilance and Clinical trial needs in the global arena.
We provide the expertise, skills, and objectivity to help evaluate, build safety systems, prepare quality submissions, maintain regulatory compliance in safety issues, and expedite on timely reporting and submissions pertaining to Pharmacovigilance. The expertise, methodology, and experience of our team inspired us to extend our competencies into Clinical Trials along with medical writing and Clinical data management services.
Our team comprises remarkably competent professionals with a combined experience of more than 50 years at leading organizations. The team members selected for each project are driven by expertise in their respective areas. Our work, reports, and follow-up activities are tailored to meet each of our sponsor’s needs. We build partnerships based on mutual respect, common interest, and complementary strengths.