Interview – How vaccines hit the market – a look behind the scenes
My interview with EvidentIQ CEO Andreas Weber These days we see a lot of critical coverage of the approval of new vaccines in numerous markets. The reporting of
EDC
One size does not fit all
Safety Notification
RTSM
Deliver powerful randomization methods
CODER
Fast and accurate clinical coding
Drug and Device Logistics
Mitigate risk and create closer connections
eTMF
Essential document collection
CTMS
Accelerate your trial and ensure data integrity
eCONSENT
Meet patients where they are
eCOA
Faster, cleaner and more reliable data
Patient Poll
Quick insights from patients
eCRF Setup
Capture better data, faster
eTMF Setup
Get up and running in no time
PV Management
Identify and handle your safety management needs
Data Management
Make more informed business decisions
Managed Service Model for MDR
Migration, Consulting and Customization for your MDR
Submission and Data Mapping
Move and consolidate data
eTechnology Strategy
Integrate and capitalize on critical technologies
Protocol Development
Turning your research question into a study
Observational Studies
Digital, cost effective and time efficient
Primary Market Research
Direct to patient, unique, and quality data
IRB and EC Management
End to end regulatory management
PV and GDPR Compliance
Safety, consent and data protection
Scientific Communications
Results dissemination
Digital Communications
Increase patient awareness
Data Linkage
Generate, combine and analyze data
My interview with EvidentIQ CEO Andreas Weber These days we see a lot of critical coverage of the approval of new vaccines in numerous markets. The reporting of
The global usage of the clinical trial management system (CTMS) is increasing thanks to its outcome’s significance and efficiency. It lessens the cost of the
The European Medicines Agency updated the Clinical Trial Regulation (Regulation EU No. 536/2014) to ensure that clinical trials are executed in the subjects’ best interest.
11am EST (NA) / 4pm GMT (UK) / 5pm CET (EU-Central) DEMYSTIFYING CLINICAL SYSTEMS INTEGRATION Clinical trials have become extremely complex, as have clinical systems.
– Takes about 6 minutes to read this topic – The U.S. FDA has implemented various programs that help to deliver safe and effective therapies
– Takes 10 minutes to read this topic – What’s the background on eCRFs? Electronic case report forms (eCRFs) are used for gathering patient data
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Commercial Register: Hamburg HRB 147319
Sales Tax Identification Number: DE312852940
Managing Directors
Andreas Weber, Manuel Neukum, Axel Jansen, Lars Kloppsteck,
Helge Hofmeister
Commercial Register: Hamburg, HRB 147319
Sales tax identification number: DE312852940
Commercial Register: Hamburg, HRB 147319
Sales tax identification number: DE312852940
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