A new working paper has found that one-third of all data points collected in 105 phase 2 and 3 trials were not needed for the ...

According to DataM Intelligence, the global pediatric clinical trials market size reached US$ 19.74 Billion in 2024 from US$ ...

According to DataM Intelligence, the global pediatric clinical trials market size reached US$ 19.74 Billion in 2024 from US$ 18.79 Billion ...

A CCS is mandated by EU and US regulations and ICH guidelines to ensure product safety and compliance in pharmaceutical manufacturing. Key CCS elements include monitoring, validation, contamination ...

Background: Consent forms have become too long and often do little to help people understand the risk elements of their participation in research, instead focusing on risk reduction for research ...

While global harmonisation remains the holy grail, the reality is that pharmaceutical companies still face significant challenges navigating regulatory differences. Stefanie Lietsch-Dallwig considers ...

American Society of Nuclear Cardiology (ASNC), European Association of Nuclear Medicine (EANM), and American College of Nuclear Medicine (ACNM) have issued a new clinical guideline for 18F-flurpiridaz ...

Oral semaglutide at a dose of 25 mg may provide an alternative treatment option to injectable semaglutide (2.4 mg) and higher-dose oral semaglutide (50 mg) for persons with overweight or obesity. In a ...

The objective is to provide guidance for pregnant women and obstetric care and exercise professionals on prenatal physical activity. The outcomes evaluated were maternal, fetal or neonatal morbidity, ...

Investigator-initiated clinical trials (IITs) are at the core of innovative thinking in health research generating data in ...