| 1 - Overview of Clinical Research.mp4 | 106.3 MB | ||
| 10 - Site Initiation for Clinical Professionals.mp4 | 78.1 MB | ||
| 11 - Site Staff Training and Oversight.mp4 | 106.1 MB | ||
| 12 - Understanding Complexity of ICF.mp4 | 77.3 MB | ||
| 13 - Monitoring Visit Coordination.mp4 | 125.1 MB | ||
| 14 - Role and Responsibilities of Study Visits.mp4 | 113.6 MB | ||
| 15 - Introduction to Regulatory Affairs.mp4 | 106.8 MB | ||
| 16 - IRB Ethics Committee Submissions.mp4 | 88 MB | ||
| 17 - Clinical Trial Protocol and Amendments.mp4 | 48.9 MB | ||
| 18 - Safety Reporting and Adverse Events.mp4 | 77.3 MB | ||
| 19 - Investigational New Drug IND.mp4 | 84.5 MB | ||
| 2 - Importance and Relevance of Clinical Research.mp4 | 157.3 MB | ||
| 20 - Regulatory Environment in Clinical Research.mp4 | 51.6 MB | ||
| 21 - Audit and Inspection in Clinical Research Contexts.mp4 | 79.1 MB | ||
| 22 - Compliance and Quality Assurance in Clinical Research.mp4 | 163.8 MB | ||
| 23 - Data Falsification and Misconduct in Clinical Research.mp4 | 181 MB | ||
| 24 - Data Validation and Verification.mp4 | 51.8 MB | ||
| 25 - Quality Assurance and Quality Control.mp4 | 51.6 MB | ||
| 26 - Standard Operating Procedures for Clinical Research.mp4 | 153.1 MB | ||
| 27 - Understanding Audits in Clinical Research.mp4 | 54.9 MB | ||
| 28 - ALCOA CCEA Principles of Documentation in Clinical Research.mp4 | 38.9 MB | ||
| 29 - Understanding Source Documentation In Clinical Research.mp4 | 107.4 MB | ||
| 3 - Key Stakeholders in Clinical Research.mp4 | 105 MB | ||
| 30 - Protocol Deviation and Medical History Management.mp4 | 171.4 MB | ||
| 31 - Treatment Visit Day 7 Protocol Deviations and Adverse Event Updates.mp4 | 81.1 MB | ||
| 32 - Understanding the Baseline Visits In Clinical Research Protocol.mp4 | 71 MB | ||
| 33 - Understanding Study Protocols and Informed Consent.mp4 | 207 MB | ||
| 34 - Understanding Clinical Research Eliciting and Updating Health Records.mp4 | 119.6 MB | ||
| 35 - CTCAE-v5.0-Reference.pdf | 2.5 MB | ||
| 35 - Understanding Adverse Events in Clinical Research.mp4 | 142.8 MB | ||
| 4 - Ethical Considerations in Clinical Research.mp4 | 44 MB | ||
| 5 - Overview of Good Clinical Practice GCP.mp4 | 55 MB | ||
| 6 - Clinical Research Terminology For NonHealthcare Professionals.mp4 | 42.1 MB | ||
| 7 - Introductions To Data Collection Management.mp4 | 94.5 MB | ||
| 8 - Overview of Clinical Research Coordination.mp4 | 75.1 MB | ||
| 9 - Site Selection and Qualification.mp4 | 63.9 MB | ||
| Bonus Resources.txt | 409.6 B | ||
| Get Bonus Downloads Here.url | 204.8 B | ||
| ▲ 38 total files | |||
Clinical Research Essentials: A Beginner'S Blueprint
https://CourseWikia.com
Last updated 4/2024
MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 3.30 GB | Duration: 6h 1m
Unlock the Mysteries of Clinical Trials and Medical Research – No Experience Needed!
What you'll learn
Introduction to Clinical Research Overview Importance and Relevance
Understanding Clinical Research History, Regulations and Global Requirements
Dissect the importance of Drug Discovery in today's medical practice.
Learn the basics of clinical study design
Differentiate between the different clinical trial types and phases.
Understanding the importance of the different roles and responsibilities in clinical research conduct.
Requirements
No previous healthcare experience is required.
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