{"id":4117,"date":"2017-10-12T07:39:21","date_gmt":"2017-10-12T05:39:21","guid":{"rendered":"https:\/\/blogdelarechercheclinique.com\/?p=4117"},"modified":"2025-05-21T11:52:41","modified_gmt":"2025-05-21T09:52:41","slug":"3-priorites-oublier-monitoring","status":"publish","type":"post","link":"https:\/\/blogdelarechercheclinique.com\/en\/3-priorites-oublier-monitoring\/","title":{"rendered":"The 3 priorities not to be forgotten in monitoring"},"content":{"rendered":"<p><iframe data-src=\"https:\/\/www.youtube.com\/embed\/PkQ11ru549w\" width=\"560\" height=\"315\" frameborder=\"0\" allowfullscreen=\"allowfullscreen\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" class=\"lazyload\" data-load-mode=\"1\"><\/iframe><\/p>\n<p class=\"p1\"><em>Article written by the Pharmaspecific Society, a specialist in clinical research.<\/em><\/p>\n<p>Hello! This is Vanessa Montanari from the clinical research blog.<\/p>\n<p>Today, I&rsquo;m making a video to give you the three (3) important things to check at the first monitoring visit.<\/p>\n<p><!--more--><\/p>\n<p>There are three (3) things that are really important.<\/p>\n<p>First of all, it&rsquo;s the SAE (serious adverse events). Sometimes it can be difficult to check this immediately when you&rsquo;re on site. But the best thing is to question your investigator as soon as you arrive. For example, ask him\/her if there have been any hospitalizations or important events during the patient&rsquo;s treatment. What you can also do is look without the medical record, but that can sometimes take a little time. Time to get to the part where the patient might have been hospitalized or had an event that could be reported as a \u00ab\u00a0serious adverse event. \u00bb<\/p>\n<p>Next, you have a very important element: consents. You will check the consent of all patients before you open the patient medical file. If the patient has not signed a consent, you are not allowed to look at the patient&rsquo;s medical record.<\/p>\n<p>Finally, the third thing, which is also very important, are the inclusion and exclusion criteria. You&rsquo;re going to look at whether the patient has the criteria to participate in the study or whether he or she should not have been included in this study. That&rsquo;s also a third thing to look at.<\/p>\n<p>So, when you go into monitoring, the three (3) things to check in order are:<\/p>\n<p>&#8211; Consents<\/p>\n<p>&#8211; CASs<\/p>\n<p>&#8211; Inclusion criteria<\/p>\n<p>I hope this little video helped you.<\/p>\n<p>See you soon! Goodbye! Bye!<\/p>\n<hr \/>\n<p>You need a<strong> service in clinical research? Contact PHARMASPECIFIC <\/strong>by visiting our website by clicking here<strong>: <a href=\"https:\/\/pharmaspecific.com\/devis\/.\">https:\/\/pharmaspecific.com\/devis\/.<\/a><\/strong><\/p>\n<p>If you have questions about being a clinical research associate or a career in clinical research, you can put them in the comments below. We will respond to you as soon as possible.<\/p>\n<p>If you want to be coached, if you want a personalized answer to your questions or if you want to be in contact with other clinical research professionals, you can go to <a href=\"https:\/\/pharmaspecific-training.com\/.\">https:\/\/pharmaspecific-training.com\/.<\/a>{:}<\/p>","protected":false},"excerpt":{"rendered":"<p>Today, I&rsquo;m making a video to give you the three (3) important things to check at the first monitoring 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