{"id":2765,"date":"2022-03-08T09:20:16","date_gmt":"2022-03-08T08:20:16","guid":{"rendered":"https:\/\/www.we4cr.com\/site-initiation-visit-siv\/"},"modified":"2025-09-01T15:52:24","modified_gmt":"2025-09-01T13:52:24","slug":"site-initiation-visit-siv","status":"publish","type":"glossary","link":"https:\/\/www.we4cr.com\/it\/glossary\/site-initiation-visit-siv\/","title":{"rendered":"Site Initiation Visit (SIV)"},"content":{"rendered":"

The Site Initiation Visit (SIV) is a meeting arranged and conducted by Sponsor team or its delegate to train the study personnel on the study procedures and Good Clinical Practice and regulatory requirements. The SIV is the last step before the start of the trial. After the following condition have been met, is it possible to schedule a SIV and open the site:
\n\u0095\tEthic Commettee approval;
\n\u0095\tSigned Clinical Trial Agreement;
\n\u0095\tInsurance;
\n\u0095\tGreenlight from Research and Development Department or equivalent (if applicable);
\n\u0095\tTrial Master File\/ Investigator Site File shipped to the site;
\n\u0095\tInvestigational product shipped to the site (if applicable).<\/p>","protected":false},"featured_media":0,"template":"","meta":{"footnotes":""},"glossary_category":[],"class_list":["post-2765","glossary","type-glossary","status-publish","hentry"],"yoast_head":"\nSite Initiation Visit (SIV) | We4 Clinical Research<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.we4cr.com\/it\/glossary\/site-initiation-visit-siv\/\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Site Initiation Visit (SIV) | We4 Clinical Research\" \/>\n<meta property=\"og:description\" content=\"The Site Initiation Visit (SIV) is a meeting arranged and conducted by Sponsor team or its delegate to train the study personnel on the study procedures and Good Clinical Practice and regulatory requirements. 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