Anova IRM Stem Cell Center & Research Laboratory

If you need additional information about Anova IRM Stem Cell Center, please

feel free to give us a call or simply contact us by e-mail by using the

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Anova Institute for Regenerative Medicine - Stem Cell Center

Strahlenberger Straße 110
63067 Offenbach am Main
Mail: This email address is being protected from spambots. You need JavaScript enabled to view it.
Tel.: +49 (69) 50 50 00 944
Fax: +49 (69) 50 50 00 980

Disclaimer: Information contained in the website is not to be considered as the provision of medical advice for specific cases and/or individual patients. Readers intent on undergoing treatment, or those assisting someone in their care, are responsible for obtaining verification of the potential outcome of treatment from their physician or suitably qualified medical professional.
Neither Anova IRM Stem Cell Center nor any of its directors, shareholders, employees, agents or representatives shall be liable for any harm, loss, injury, death, disability, adverse reactions, ineffectiveness, complications or other medical accidents or events arising from, or in connection with, the publication of, use of or reliance upon any information, advice, products and / or services contained on this website or which may be promoted, displayed on, or associated with, our website or any other website which can be accessed from this website. The information contained on our website represents the opinions of the authors and editors and should not be defined to be the position of any regulatory agencies or governments unless cited directly.

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Code of Operation, Integrity, Ethical and Legal Framework

Anova IRM works strictly within the German and European legal framework in an ongoing dialog with the German Governement’s regulatory bodies. Use and strategy of any therapy is decided on an individual basis and explicit informed consent with the patient. The Anova clinic operates in full ISO9001 compliance.

Regierungspräsidium Hessen: Darmstadt regional authority
Paul Ehrlich Institute: Federal regulatory authority
European Medicines Agency: Laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use
Gesetz über den Verkehr mit Arzneimitteln (Arzneimittelgesetz - AMG): Legal framework for trafficing pharmacutical products
Good Manufacturing Practice: Laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human use
Advanced Therapy Medicinal Products: Amending Directive 2001/83/EC and Regulation (EC) No 726/2004
Good Clinical Practice: Laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use. Also regulating clinical trials for human use.
ISO9001: Defining fundamentals of quality systems, among others for medical institutes.
Medicinal Product for human use: Amending Directive 2001/83/EC on the Community code
Medical Devices: Council Directive regulating medical devices

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Strahlenberger Straße 110
63067 Offenbach am Main

Tel.: +49 (69) 50 50 00 944

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