Our Regulatory Portfolio

At VJ BIO FARMA, we assist our suppliers throughout the complete lifecycle of preparing and submitting regulatory applications for APIs, Finished Formulations, and Medical Devices as per specific client requirements. Our qualified regulatory experts meticulously review, compile, and submit documentation for clients in full compliance with DCGI guidelines. Additionally, our team helps streamline documentation, ensures alignment with evolving regulatory standards, and facilitates smooth communication between manufacturers and regulatory bodies.