Women account for nearly half the human population (49.6%), but are often excluded from clinical trials and medical research. Unfortunately, this lack of inclusion has real-world consequences. A recent study published in the Annals of Internal Medicine found that…
Pro Tips for Creating a Successful Informed Consent Form (ICF) The informed consent form (ICF) is one of the most crucial documents sponsors draft for clinical trials. For many potential enrollees, the ICF is their first introduction to clinical…
Preparing for ICH GCP E6 R3 The International Council for Harmonization’s (ICH) guidelines received a major update in 2023 with the introduction of ICH E6(R3). This new protocol provides an outline for ensuring patient safety and data quality during…
