9 Pro Protocol test planning Estimated reading: 1 minute 639 views Authors PRO/01 Contract reviewDownload PRO/02 Test designDownload PRO/05 Data collection and description of active ingredientsDownload Pro/06 Exchange of information between clinical pharmacologist and head of clinical trialDownload PRO/08 Timetable PRO/09 Creation and approval of a test planDownload PRO/09-01 Form for test planDownload PRO/10 Modification of a test planDownload PRO/10-01 Amendments to a test planDownload PRO/11 Investigator's BrochureDownload PRO/11-01 Table of contents investigagor brochure PRO/12 Creating and maintaining a checklist (CRF)Download PRO/12-01 CRF sampleDownload PRO/13 Preparation of information sheet and declaration of consentDownload PRO/13-01 Sample information sheetDownload PRO/13-02_ Declaration of consentDownload PRO/13-03 Sample consent for radioactive substanceDownload PRO/14 Study planDownload PRO/15 Obtain ethics voteDownload PRO/15-01 Cover letter Ethics CommitteeDownload PRO/16 Entry in the Clinical Trials Register Clinical Trial Manual - Previous 8 CSP Provided products Next - Clinical Trial Manual 10 PRC Process Control Process Control Monitoring
