If you are looking to navigate the complex regulatory environment in China, particularly concerning the reporting requirements for clinical trials and post-authorization processes, IntuVigilance is here to assist you.

We are excited to announce that IntuVigilance has established a presence in China, offering comprehensive regulatory affairs and drug safety / pharmacovigilance services. Our expertise is designed to help you overcome the challenges associated with compliance and reporting, ensuring that your operations align with local regulations and standards.

We can manage the intricacies of regulatory requirements, providing you with peace of mind in a rapidly evolving landscape.