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Kathy Barnett
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3:19
Clinical Trial Start-Up: Using a Work Breakdown Structure (WBS) for Effective Planning
14 дней назад
1:49
Building QbD and RBQM Systems into Clinical Operations
14 дней назад
3:44
Inspection Readiness: Understanding BIMO Inspection Req for Sponsors, CROs, Monitor, Investigators
3 месяца назад
4:09
ICH E8 (R1): Designing Quality into Clinical Studies
3 месяца назад
2:18
Trial Master File (TMF) for Sponsors: Set Up and Maintenance
3 месяца назад
2:03
Approaches to Address Challenges in Vendor Management
3 месяца назад
2:09
Corrective Action Plans: Essential Documentation of a Site’s Response to GCP Deficiencies
3 месяца назад
5:07
Managing Phase I Clinical Trials
3 месяца назад
3:00
CRO Partner Management
3 месяца назад
4:30
Overseeing Teams and Projects
3 месяца назад
2:17
Introduction to Statistics for Non-Statisticians
4 месяца назад
2:29
ICH GCP E6 R2 and R3 Updates Implementing Risk Management Approaches for Compliance
4 месяца назад
5:01
Good Clinical Practice: A Question & Answer Reference Guide 2024/2025
6 месяцев назад
2:37:33
Introduction to Statistics for Non Statisticians
9 месяцев назад
3:45
ICH E6 (R3) and ICH E8 (R1)Updates: Impact on Sponsors
9 месяцев назад
6:46
FDA’s Bioresearch Monitoring (BIMO) Program: Inspection of Sponsors, CROs, and Monitors
Год назад
7:26
ICH GCP E6 R2 and R3 Updates: Implementing Risk Management Approaches for Compliance
2 года назад
6:49
ICH E6 (R3) and ICH E8 (R1) Updates: Impact on Sponsors
2 года назад
6:55
Developing Clinical Study Budgets for Sponsors
2 года назад
7:03
Risk-Based Monitoring & Quality Mgmt of Clinical Trials: Recent Guidance Updates from FDA & EMA
2 года назад
6:58
ClinicalTrials.Gov Requirements
2 года назад
7:05
Electronic Medical Records: Approaches for Ensuring Source Document & 21 CFR Part 11 Req. Components
2 года назад
7:19
Investigator Initiated Trials: Roles and Responsibilities
2 года назад
6:01
Electronic Informed Consent Guidance: Regulatory Updates
2 года назад
6:15
Ensuring Success Through Smarter Site Selection and Study Feasibility
2 года назад
6:01
Strategies for Managing Difficult Clinical Research Sites
2 года назад
6:27
TMF/eTMF Audit Strategies
2 года назад
6:13
Trial Master File (TMF) for Sponsors: Set Up and Maintenance
2 года назад
7:06
ICH E8 (R1): Changes Impacting Sponsors/CROs
2 года назад
Комментарии
@blesssings1568
7 лет назад
Great information.
@abdulraheem6983
7 лет назад
you are provide good information for people who are in confusion those guys are bene
@Untainted786
9 лет назад
You provide very beneficial information. Please post the other videos that cover the objectives at the front.
@kathybarnett4070
9 лет назад
+Waff25 Hi there - this is merely a preview of our DVDs and web seminars. To purchase this DVD go to: bit.ly/1FN0Kk1 To attend our web seminar in January on this topic visit: bit.ly/1KW8htR Thanks!
@Untainted786
9 лет назад
Kathy Barnett Okay, thank you