Скачать с ютуб The Only Crash Course To Clinical Research You’ll Ever Need (full 5 hour OFFICIAL video) в хорошем качестве

The Only Crash Course To Clinical Research You’ll Ever Need (full 5 hour OFFICIAL video)

The Only Comprehensive Guide To Clinical Research You’ll Ever Need (full 5 hour crash course) v.2019 (Make sure to watch in 1080p to avoid the lip sync lag) GET THE BOOK! https://www.amazon.com/dp/1090349521/... Join this channel to get access to perks:    / @dansfera   Text Me: (949) 415-6256 My podcast is Random Musings From The Clinical Trials Guru Listen on Spotify: https://open.spotify.com/show/7JF6FNv... GET THE BOOK! https://www.amazon.com/dp/1090349521/... Text "guru" to 855-942-5288 to join VIP list! My blog: http://www.TheClinicalTrialsGuru.com My CRO and Site Network: http://www.DSCScro.com My CRA Academy: http://www.TheCRAacademy.com My CRC Academy: http://www.TheCRCacademy.com Latinos In Clinical Research: http://www.LatinosinClinicalResearch.com The Clinical Research Circle:    / @theclinicalresearchcircle6001   My TikTok: DanSfera Timepoints 00:00 Intro To Crash Course To Clinical Research 02:24 Bird’s Eye View of Clinical Research 03:21 What/Who is a Sponsor? 04:09 Types of Sponsors 05:02 Intro to Clinical Trials, Phases and Sites 09:04 Research Protocols 10:08 Who Works at Investigate Sites? 11:24 Contract Research Organizations (CROs) 15:27 FDA, GCP, IRBs and Ethics 23:10 What are Vendors and Electronic Data Capture (EDC)? 29:16 Clarifying Private Vs Academic Sponsors 35:54 CRCs and CRAs - The Backbone of Clinical Research 43:37 What Do CRCs Actually Do? (1) 47:53 Intro to Source Documents 49:30 What Do CRCs Actually Do? (2) 53:41 What is ALCOA-C? 1:01:00 What Do CRAs Actually Do? 1:08:24 How Do You Become a CRA? 1:15:29 What Are Other Entry Jobs At Sites? 1:16:58 Lead CRAs & Line Managers 1:18:49 In-Depth View: Clinical Phases; Phase I 1:23:48 Phase II Studies 1:30:02 Phase III Studies 1:40:11 Phase IV 1:44:22 ICH Principles - Cornerstone of Clinical Research Ethics 1:59:31 Training, Certificates & More Practical Aspects 2:04:16 Regulatory Start-up 2:15:26 Regulatory Maintenance 2:22:52 Protocol Amendments 2:27:20 What Does AEs, SAEs & SUSAR Mean? 2:36:05 In-Depth View: Source Documents 2:41:30 What is Informed Consent? 2:50:44 Two Clinical Aspects to Rule Them All 2:51:43 Medical History 2:56:19 I/C CRITERIA & Subject Confidentiality 2:59:44 In-Depth View: Adverse Events (AEs) 3:07:48 What Does ‘Breaking The Blind’ Mean? 3:09:22 Protocol Deviations 3:13:08 Schedule of Assessments 3:15:21 What Are the Types of Clinical Research Visits? 3:21:03 Visit 2/Randomization 3:28:28 Routine Study Visits 3:32:48 What Can Site Do To Reach Patients? 3:34:52 Screen Failure 3:37:53 Intro to Monitoring Visits 3:48:06 In-Depth View: SDV/SDR 3:55:01 In-Depth View: Monitoring Visits 4:16:38 OUTRO