Go ahead for PASSPORT-HF by ethics committee
The ethics committee has evaluated the clinical investigation plan and has provided favourable opinion for the PASSPORT-HF study without further requirements.
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Your publications are your success
We have only done our job well if you are successful.
Trust in data
Your data is ready. It has been checked, cleaned up and is now in a standardised format. We evaluate your data together with you. You ask the questions and we provide the analysis.
You can rely on the quality of your data and your results.
Publish and present
We work together with you on your presentations and publications. You can rely on us in review processes too. We are experts in the field and we specialise in cardiovascular diseases. We are able to work closely with you to provide fast responses, check everything one last time and answer any remaining questions.
We’ll also work late into the night to do this when necessary.
Your idea - your success
We congratulate you and celebrate with you. And we are already looking forward to your next idea.
Services
Integrated randomisation
Data Management Plans
GCP requirements
Interim/final reports
CRF design
Status reports
Survival analyses
Fully automatic edit checks
Law on the Reorganisation of the Pharmaceutical Market (AMNOG) reports
Data Validation Plans
Hypothesis testing
Publication manuscripts
Data Export Plans
21 CFR Part 11
Descriptive analyses
Line listings
Lecture manuscripts
DSMB support
Query management
Data review
Multivariate models
News
First COVID-19 Registry in Rhineland-Palatinate, Germany
Supported by the Ministry of Social Affairs, Labour, Health and Demography of Rhineland-Palatinate, IHF GmbH manages the COVID-19-Registry Rhineland-Palatinate, which was launched this weekend. Registry for Rhineland-Palatinate for the documentation...
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Benefit assessment of an innovative medical device: A study commissioned by the Federal Joint Committee (G-BA)
Commissioned by the Federal Joint Committee (G-BA), IHF GmbH is running one of the first studies on benefit assessment of a medical device in accordance with the directive § 137e Social Security Code Book V (SGB V).
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