In the last 47 years, we have successfully conducted over 3,200 clinical trials and boast with successful regulatory inspections by the FDA, EMA, MHRA and WHO to name a few, confirming our compliance with international clinical research standards. By remaining flexible and offering real-time quality solutions we have gained the trust of our loyal international client base. At FARMOVS we conduct ICH-GCP compliant Phase I to IV clinical trials, Bioequivalence Studies, with additional Patient Recruitment, a Licensed Pharmacy and Depot services. We also have a dedicated Site Management Organisation team that collaborates with our well-established external network investigator sites. As a result, our clients gain the benefits of access to a uniquely diverse study population and the uninterrupted continuation of their studies despite the impact or challenges of the Covid-19 pandemic. Our on-site GLP accredited Bioanalytical Laboratory, ISO 15189 accredited Safety Laboratory and large Clinic Facilities enables increased operational efficacy. You can also gain the competitive advantage that your study needs. Contact us today!
Phone: +27 51 410-3179/3452
E-mail: business@farmovs.com
Web: www.farmovs.com
Add：Pharmacology Building, University of the Free State, Nelson Mandela Drive, Bloemfontein, 9301
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微信号：csco2022
公众号：康安医药咨询
