by cwrm | July 22, 2025 | Generally
Why the revision from R2 to R3 is a turning point The revision of ICH E6 from version R2 to R3 marks a significant turning point: The guideline is being fundamentally modernized – with a stronger patient focus, digitalized processes, risk-based...
by cwrm | May 15, 2025 | Generally
Deep Learning in Clinical Research Deep learning, a subfield of machine learning, uses artificial neural networks to analyze complex data structures and is therefore a subfield of artificial intelligence (AI). In clinical research...
by weissblau media | Jan 14, 2025 | Generally
The Challenge of Patient Recruitment Finding patients for clinical trials is a complex process that presents several hurdles. The following challenges often complicate the recruitment process: Strict inclusion and...
by weissblau media | Jan 14, 2025 | Generally
Why are clinical trial costs rising? Clinical trials are inherently demanding. The need to meet all regulatory requirements, collect comprehensive data, and ensure participant safety makes them...
by weissblau media | Jan 14, 2025 | Generally
The most important regulations for clinical trials: Declaration of Helsinki: This declaration of the World Medical Association formulates ethical principles for medical research involving human subjects and serves as an ethical guideline for clinical trials. Good Clinical Practice...
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