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Thieme-Compliance

Certificate

Our Quality Management System is certified by following standards:

 

EN ISO 13485:2003+AC:2009

 

DIN EN ISO 9001:2008

About us

Patient consent forms are used as an aid in the pre-operative discussion that must take place between doctor and patient.

The forms serve as the – legally required – evidence that the patient consents to the treatment. Millions of our forms are used by doctors every year in printed and electronic form.

Thieme Compliance is the market leader in the legally validated patient consent form market in Germany. 

Thieme Compliance markets patient information materials for more than 2,000 different diagnostic and surgical procedures in up to 13 languages.

Safety, always up to date

It is vital, that a patient is fully informed about the chances and risks of an upcoming operation to gain the patients‘ confidence and ensure their satisfaction – wherever in the world the operation takes place. 

Our patient education and informed consent documents are constantly being reviewed, updated and improved taking into account international patient safety regulations and the latest diagnostic and therapeutic methods.

History

2010
Thieme Compliance develops the software E-ConsentPro as a complete and integrated solution in the field of legally profound patient education. E-ConsentPro integrates all Diomed and proCompliance patient education forms available in one software.

2008
Thieme Compliance takes the next step to establish itself as a system provider for integrated patient education solutions by adopting and revising Medlinq's education films for anaesthetics.

2006
DIOmed and proCompliance are united under Thieme publishers (2007 Thieme Compliance) and still keep their existence as brands.

1981
The predecessor of proCompliance is founded.

1979
The first standardized patient consent form is drafted and published by the founding editors in the field of anaesthetics.



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