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3 Tips for Improving Your Clinical Trial Site Selection Process Selecting a site (or sites) to host your next clinical trial is crucial to your

5 Areas Where CROs Are Making a Difference in Rare Disease Research Rare disease research is becoming increasingly crucial for the biopharmaceutical industry. Several factors

5 Tips for Embracing eConsent Adoption While Keeping Patients at Top of Mind Electronic informed consent (eConsent) technologies have been around for nearly 20 years,

In April, The U.S. Food and Drug Administration (FDA) released three draft guidance documents focused on increasing participation and diversity in oncology clinical trials. The

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

What You Need to Know About the FDA and OHRP’s Joint Draft Guidance on Informed Consent in Clinical Trials  All FDA-regulated clinical investigations of drugs,