Label
Search
SKIP TO CONTENT
SKIP NAVIGATION
Patient Resources
COVID-19 Patient Resource Center
Clinical Trials
Search Clinical Trials
Patient Notification System
What is Clinical Research?
Volunteering for a Clinical Trial
Understanding Informed Consent
Useful Resources
FDA Approved Drugs
Professional Resources
Research Center Profiles
Clinical Trial Listings
Market Research
FDA Approved Drugs
Training Guides
Books
eLearning
Events
Newsletters
White Papers
SOPs
eCFR and Guidances
White Papers
Trial Listings
Advertise
COVID-19
iConnect
Sign In
Create Account
Sign Out
My Account
Home
» Vendor Qualification Critical to Patient Safety, Data Quality and GCP Compliance
Looking to read the full article? Subscribe today!
Vendor Qualification Critical to Patient Safety, Data Quality and GCP Compliance
January 28, 2022
Elizabeth Tilley Hinkle
To operate in a state of control and ensure the validity of their trials and the safety of their patients, sites must be keenly aware of and monitor vendors’ participation.
Upcoming Events
16
Feb
Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success
21
May
WCG MAGI Clinical Research Conference – 2023 East
Featured Products
Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant
Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs
Featured Stories
Sites Name Tech Acceptance as Essential Factor in Selection of Sponsors, Survey Finds
WCG Clinical Research Trends and Insights for 2023, Part Two
Time is Money and So Is Effort, Budgeting Experts Say
WCG Clinical Research Trends and Insights for 2023, Part Three
Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials
The information you need to adapt your monitoring plan to changing times.
Learn More Here