Once a drug successfully moves through clinical trials, regulatory bodies review the data to assess the drug’s clinical efficacy against the disease and whether it is well tolerated in humans. 8 A ...

Lynn Jagodzinski CTSI Clinical Research Regulatory Administrator (716) 888-4843 [email protected] Urmo Jaanimägi CTSI Quality Assurance Specialist (716) 888-4760 [email protected] Here is where ...

Europe conference, which took place between 29 and 30 April in Barcelona, Spain, industry experts delivered comprehensive insights, examined emerging trends and tackled regulatory and operational ...

A new study by investigators from Europe, including the Netherlands and the United Kingdom (UK), has shed light on ...

The Clinical Data Interchange Standards Consortium (CDISC) is dedicated to the improvement of medical research through data standardization. CDISC has produced a suite of standards that should be ...

A new study by investigators from Europe, including the Netherlands and the United Kingdom (UK), has shed light on ...

MDC Associates, a leading provider of clinical and regulatory consulting services for the MedTech industry, has announced a significant expansion of its MedTech clinical solutions designed to help ...

The move came following allegations levelled by Justice P Krishna Bhat (Retd), former chairperson of Institutional ethics ...

Karnataka govt informs DCGI to probe into 'unfair clinical trials' at HCG: Our Bureau, Bengaluru Wednesday, July 2, 2025, 11:10 Hrs [IST] Karnataka government has written to the D ...

The Karnataka government has asked the Central Drugs Standard Control Organisation to investigate alleged clinical trial ...