Medicines and Healthcare products Regulatory Agency
Register
Help
Remember Me?
Forgot login details?
Forum
FAQ
Forum actions
Mark all forums as read
Quick links
What's new?
Advanced Search
Forum
Good Clinical Practice (GCP)
Investigator Sites (inc Principal Investigator responsibilities, consent, source data and CRFs)
Electronic Source Data Access for Monitors and Inspectors
You will need to register or login above with your username to post on this forum.
If you require further help please view our
quick start guide
or view the
online help
section.
Results 1 to 9 of 9
Thread:
Electronic Source Data Access for Monitors and Inspectors
Thread Tools
Show Printable Version
Email this Page…
Search Thread
Advanced Search
Display
Switch to Linear Mode
Hybrid Mode
Switch to Threaded Mode
Hybrid View
Previous Post
Next Post
7th Feb 2021,
07:48 PM
#1
a123456
View Profile
View Forum Posts
Private Message
Forum Member
Join Date
Nov 2011
Posts
183
Brilliant news. Is this system part of a normal NHS system or something brought in?
Reply With Quote
Quick navigation
Investigator Sites (inc Principal Investigator responsibilities, consent, source data and CRFs)
Top
Site Areas
Settings
Private messages
Subscriptions
Who's online
Search Forums
Forums Home
Forums
Good Clinical Practice (GCP)
GCP Forum introduction and rules - PLEASE READ BEFORE POSTING ON THIS FORUM
Clinical laboratories
Computer system validation (CSV) and IT systems
Contracts and agreements (including insurance)
Data management
Electronic Systems (inc. e-CRF, e-source, ePRo and ehealth records/EHR)
Equipment maintenance
Ethics approval
Inspection process
Investigational Medicinal Products (IMP)
Investigator Sites (inc Principal Investigator responsibilities, consent, source data and CRFs)
Legislation
Monitoring
Pharmacovigilance
Programme management
Quality Systems (including QA, SOP and Training)
Risk adaptive approach
Risk-based inspections
Regulatory documents (including protocol, clinical study reports and publications)
Sponsor oversight
Statistics
Trial Master File (TMF) and archiving
Blood Forum
Blood Forum introduction and rules - PLEASE READ BEFORE POSTING ON THIS FORUM
Quality Management
Personnel & Organisation
Premises
Change Control / Validation
Documentation
Computerised Systems
Blood Collection, Testing & Processing
Storage & Distribution
Contract Management
Non-Conformance (Deviations / Investigation / CAPA / Root Cause Analysis / Complaints / Recall)
Self-Inspection
Regulatory Inspections
Quality Monitoring & Control
Haemovigilance & SABRE
Legislation / Guidelines
Blood Consultative Committee
Links
«
Previous Thread
|
Next Thread
»
Posting Permissions
You
may not
post new threads
You
may not
post replies
You
may not
post attachments
You
may not
edit your posts
BB code
is
On
Smilies
are
On
[IMG]
code is
On
[VIDEO]
code is
On
HTML code is
Off
Forum Rules
Posting Permissions
Reply With Quote