oaxino Posted April 19 Report Share Posted April 19 Clinical Research Essentials: A Beginner'S BlueprintLast updated 4/2024MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHzLanguage: English | Size: 3.30 GB | Duration: 6h 1mUnlock the Mysteries of Clinical Trials and Medical Research - No Experience Needed!What you'll learnIntroduction to Clinical Research Overview Importance and RelevanceUnderstanding Clinical Research History, Regulations and Global RequirementsDissect the importance of Drug Discovery in today's medical practice.Learn the basics of clinical study designDifferentiate between the different clinical trial types and phases.Understanding the importance of the different roles and responsibilities in clinical research conduct.RequirementsNo previous healthcare experience is required.DescriptionDive into the dynamic world of clinical research with our comprehensive course designed exclusively for beginners! "Clinical Research Essentials: A Beginner's Blueprint" offers a step-by-step guide to understanding the fundamentals of clinical trials and medical research processes. Whether you aspire to a career in healthcare, wish to join the pharmaceutical industry, or simply have a keen interest in science, this course is your gateway to mastering the basics.In this course, you will learn:Key Concepts of Clinical Research: Discover what clinical research entails and why it's crucial for medical advancements.The Design of Clinical Trials: Understand the methodologies behind setting up and conducting clinical trials.Ethical Considerations: Learn about the ethical standards and why they're essential in protecting study participants.Data Handling and Analysis: Gain insights into how data is collected, analyzed, and used to make evidence-based decisions.Regulatory Framework: Familiarize yourself with the regulatory environment that governs clinical research globally.Designed with the novice in mind, each module features easy-to-understand content supported by real-world examples, and additional resources to ensure a thorough learning experience. By the end of this course, you will not only gain a solid foundation in clinical research but also develop the confidence to contribute to life-saving research and perhaps even pursue further studies or career opportunities in this vital field. You will be skillful and qualified enough to apply the skills you have learnt in a Clinical Research Assistant role.Enroll in "Clinical Research Essentials: A Beginner's Blueprint" today and start your journey into the world of clinical research with confidence!OverviewSection 1: Introduction To Clinical ResearchLecture 1 Overview of Clinical ResearchLecture 2 Importance and Relevance of Clinical ResearchLecture 3 Key Stakeholders in Clinical ResearchLecture 4 Ethical Considerations in Clinical ResearchLecture 5 Overview of Good Clinical Practice (GCP)Lecture 6 Clinical Research Terminology For Non-Healthcare ProfessionalsLecture 7 Introductions To Data Collection & ManagementLecture 8 Overview of Clinical Research CoordinationSection 2: Clinical Research Monitoring VisitLecture 9 Site Selection and QualificationLecture 10 Site Initiation for Clinical ProfessionalsLecture 11 Site Staff Training and OversightLecture 12 Understanding Complexity of ICFLecture 13 Monitoring Visit CoordinationLecture 14 Role and Responsibilities of Study VisitsSection 3: Regulatory Compliance In Clinical ResearchLecture 15 Introduction to Regulatory AffairsLecture 16 IRB Ethics Committee SubmissionsLecture 17 Clinical Trial Protocol and AmendmentsLecture 18 Safety Reporting and Adverse EventsLecture 19 Investigational New Drug (IND)Lecture 20 Regulatory Environment in Clinical ResearchSection 4: Quality Assurance and Quality Control In Clinical ResearchLecture 21 Audit and Inspection in Clinical Research ContextsLecture 22 Compliance and Quality Assurance in Clinical ResearchLecture 23 Data Falsification and Misconduct in Clinical ResearchLecture 24 Data Validation and VerificationLecture 25 Quality Assurance and Quality ControlLecture 26 Standard Operating Procedures for Clinical ResearchLecture 27 Understanding Audits in Clinical ResearchSection 5: Clinical Research Patient Visits & Protocol ManagementLecture 28 ALCOA CCEA Principles of Documentation in Clinical ResearchLecture 29 Understanding Source Documentation In Clinical ResearchLecture 30 Protocol Deviation and Medical History ManagementLecture 31 Treatment Visit Day 7 Protocol Deviations and Adverse Event UpdatesLecture 32 Understanding the Baseline Visits In Clinical Research ProtocolLecture 33 Understanding Study Protocols and Informed ConsentLecture 34 Understanding Clinical Research Eliciting and Updating Health RecordsLecture 35 Understanding Adverse Events in Clinical ResearchBeginners in clinical research and drug development,Non healthcare individuals interested in a career in clinical research.Screenshotsrapidgator.net:https://rapidgator.net/file/4b4d24fd105d2ff9c3a215fc3cece323/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part1.rar.htmlhttps://rapidgator.net/file/ea1649e04c24fc0a19cef019c02bb456/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part2.rar.htmlhttps://rapidgator.net/file/678bbce5b96ce3c44e95c7dceb95023d/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part3.rar.htmlhttps://rapidgator.net/file/617cf488cc0b5d0a4242ff20b10ff849/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part4.rar.htmlnitroflare.com:https://nitroflare.com/view/1E917EF8D27EFFF/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part1.rarhttps://nitroflare.com/view/3850BA0E3EEF30C/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part2.rarhttps://nitroflare.com/view/7229ECA6DC908D8/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part3.rarhttps://nitroflare.com/view/24D8132FC39AF2B/svosc.Clinical.Research.Essentials.A.BeginnerS.Blueprint.part4.rar Link to comment Share on other sites More sharing options...
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