System Implementation

At MedWatch Consulting, we specialize in establishing and maintaining compliant pharmacovigilance (PV) and medical information (MI) systems. Our goal is to ensure that your safety infrastructure is secure, efficient, and fully aligned with international regulations such as FDA, EMA, GDPR, and ICH guidelines.

From vendor selection and contracting to database setup, migration, and SOP development, we provide end-to-end support tailored to the specific needs of each organization. Whether you are a start-up implementing your first system or a global company transitioning to a new vendor, our team ensures a seamless and compliant process.

We combine technical expertise, regulatory knowledge, and practical experienceto help companies design workflows that enhance compliance, improve efficiency, and withstand the scrutiny of regulatory inspections.

Partnering with us means building a pharmacovigilance system that is not only compliant today, but also scalable and future-ready, giving you confidence as your products grow and expand into new markets.