
IntuVigilance provided EU QPPV as well as local QPPV, literature monitoring and expedited reporting services, plus support with Risk Management Plans. Their experience, knowledge and efficiency was vital to our ability to meet all requirements. They blended seamlessly into the existing PV team and very quickly became a vital part of the company.
Service Provider
Nimisha Kotecha stepped in as interim QPPV for a UK based pharmaceutical client and went through MHRA inspection with a favourable outcome. IntuVigilance provides a high quality, yet cost efficient, service to our big and small pharmaceutical clients. We highly recommend IntuVigilance to any pharmaceutical company with a regulatory presence in the EU.
Pharmaceutical company
Over the past 5 years working with the IntuVigilance team I have found them to be professional, supportive and flexible. They took the time to understand our requirements and provide us with an external drug safety department that handles our global safety database as well as ongoing study support.
PV Service Provider, EU QPPV, EudraVigilance EVWeb-XEVMPD Trainer
I have been collaborating with IntuVigilance, and specially with Nimisha, among several pharmacovigilance projects. Nimisha is hardworking, committed and a trustworthy professional, with excellent knowledge in strategic and operational pharmacovigilance - and an innovative thinker who anticipates changes in the field.
CRO
The professional support provided by IntuVigilance through Nimisha Kotecha during a period of 8 months was essential to replace ad interim the roles of Director of PV and QPPV for all our clients - bringing confidence to our clients and creating the platform for future growth.
Pharma
Our company has worked with IntuVigilance for 5 years and they have held our global safety database since 2017, functioning as our external drug safety department since then. We rely heavily on them to fill an expertise gap in our small, virtual company, and would have no hesitation recommending them.
Pharma
