😷 Patients see the treatment working.👨⚕️ Doctors see a new option becoming available.🏥 The public sees a medical breakthrough. But behind that breakthrough are years
In 1946, clinical research took a decisive leap forward with the Randomized Controlled Trial (RCT) of Streptomycin—the first RCT designed to cure a disease. The
When designing clinical trials, access to real-world patients plays a crucial role in ensuring faster recruitment, high-quality data and reliable study outcomes. Across Europe, certain
When selecting a CRO partner, internationally recognized certifications such as ISO 13485:2016 and ISO 9001:2015 provide a strong signal of reliability, compliance, and operational excellence.
During 1943–44, the UK’s Medical Research Council (MRC) ran the first modern double-blind trial in the general population, testing patulin (from Penicillium patulinum) for the
A recent article from Applied Clinical Trials highlights a critical shift: moving from simple digitization to true workflow orchestration. Despite the rapid growth of eClinical
While this marks the end of a product’s market journey, the manufacturer’s responsibilities don’t simply vanish. 📋 Even after distribution has ceased, manufacturers must retain
When planning clinical trials, access to a large, diverse, and motivated patient population is a critical success factor. Central and Eastern Europe continues to stand
J. B. Amberson, B. T. McMahon and M. Pinner conducted a groundbreaking clinical trial evaluating sanocrysin, a gold-based compound, for treating pulmonary tuberculosis. 👇 👥
Medical device documentation requires regular updates and renewal to stay compliant and ensure safety. Regulatory bodies mandate that manufacturers periodically review and revise documentation based
