With a state-of-the-art research facility, 4MCS offers high quality patient-centred clinical trials with improved commercial efficiency. Focused cost effectiveness helps the development and licensing of novel medicines in a timely manner leading to early market access, improving patient quality of life.
4MCS offers a dedicated office for sponsors’ monitors (CRA’s) to ensure uninterrupted data collection/review/monitoring, maintaining data integrity –a vital component of clinical research. Real world evidence (RWE) based access to patients is one of the key offerings of 4MCS, with loyalty being an important factor to our success.
4MCS understands the complexity of drug development and clinical research activities. With ever-changing regulatory environments, the development of new medicines and/or new indications brings about unique challenges. 4MCS has decades of experience in clinical trial programmes from initial concepts to completing phase 2-4 clinical researches and dossier submissions for marketing authorisation.
4MCS is proud of attracting high calibre research staff (doctors, research nurses, research assistants, pharmacists, laboratory technicians and data managers), IT experts and administrative team members. All staff employed by 4MCS are ICH-GCP trained and receive regular internal training to maintain the highest level of knowledge in patient care and regulatory compliance.