Phlexglobal Blog | TMF Reference Model

US +1(484) 324-7921 | UK +44 (0)1494 720420
info@phlexglobal.com
Schedule Free Consultation

Technology
Services
- Regulatory
  - Regulatory
  - IDMP Readiness
- Clinical
Solutions
Insights
Company
Contact

10 Short Years Ago, the TMF Reference Model Was Born

Almost exactly 10 years ago – on the 23rd of March, 2009 to be precise – a pretty diverse group of about 20 TMF ...

Posts by Topic

Regulatory Requirements (14)
Submissions (13)
eCTD (12)
Compliance (8)
EMA (7)
FDA (7)
IDMP (6)
TMF Health Zone (5)
SPOR (4)
ANDA (3)
DMF (3)
Health Canada (3)
Inspection Readiness (3)
RIM (3)
AI (2)
BLA (2)
CDER (2)
Cloud-Based (2)
Electronic Submissions (2)
ICH (2)
IND (2)
Life Sciences (2)
Module 1 (2)
OMS (2)
PMS (2)
RMS (2)
Regulatory Information Management (2)
SMS (2)
SaaS (2)
Software (2)
TGA (2)
eAF (2)
eCTD v4.0 (2)
Australia (1)
COVID-19 (1)
Common Errors (1)
Data Mining (1)
EU (1)
Electronic Application Forms (1)
Generic Drugs (1)
Health Authorities (1)
In-Vitro Diagnostic (1)
Information Technology (1)
Machine Learning (1)
Medical Devices (1)
NDA (1)
NeeS (1)
PSUR (1)
Pharma (1)
Swissmedic (1)
TMF Migrations (1)
TMF Reference Model (1)
Validation Rules (1)
XML Message (1)
eCTD v3.1 (1)
xEVMPD (1)

See all

Subscribe To Our Blog!

It's time to raise your standard

CONTACT PHLEXGLOBAL TODAY

About Phlexglobal

Phlexglobal provides a unique Trial Master File solution by leveraging dedicated and authoritative TMF technologies and expert services to bring order, stability, and control to your Trial Master File – helping you achieve the highest standards for completeness, timeliness, and quality.