As you look ahead to an upcoming clinical trial or evaluate the progress of your current one, you might be wondering if it’s time to ask for help.
Topics: Medical Devices CRO
You want to keep your trial on track, but physical distancing and travel restrictions have made it difficult. Fortunately, IMARC has experience providing remote services.
As you look ahead to an upcoming clinical trial or evaluate the progress of your current one, you might be wondering if it’s time to ask for help.
Topics: Medical Devices CRO
Whether on the site or sponsor level, in clinical research we are asked to use Good Documentation Practices (GDP) during the conduct of a clinical trial. One might assume that a quick visit to the FDA website would produce the list of practices. However, there is no Code of Federal Regulations for GDP.
Topics: Good Clinical Practice, Good Documentation Practices, Medical Devices CRO, FDA