BIO 2024German Exhibitors FGK Clinical Research GmbH

FGK Clinical Research GmbH

Booth number: 4315-14
www.fgk-cro.com

About us

FGK provides full service for clinical studies to biotechnology, medical device and pharmaceutical companies. FGK has the right size to handle international multi-center studies with hundreds of patients or single country studies with a few patients, but is still small enough to guarantee a personal service to the sponsor. With our 240 highly qualified medical, scientific and regulatory experts, we have all knowledge and experience necessary to succeed in Europe and can guide you through the clinical trial process, from planning and approval to the final report.

Full service or partial services for conduct of clinical trials including: 

  • clinical trial management and clinical monitoring 
  • regulatory submissions 
  • biostatistics 
  • data management 
  • eSolutions 
  • medical writing 
  • medical safety 
  • quality assurance 
  • pharmacovigilance 
  • consulting services

FGK also offers legal representation services for sponsor companies conducting trials in the EU, the UK and Switzerland without having a subsidiary there.

Address

FGK Clinical Research GmbH
Heimeranstr. 35
80339 Munich
Germany

Phone:  +49 89 8931190

Contact person:

Martin Krauss
Managing Director
E-mail: martin.krauss@fgk-cro.com

Ursula Türcke
Senior Director Clinical Operations
E-mail: ursula.tuercke@fgk-cro.com

CRO services for clinical studies

Full service or partial services for conduct of clinical trials including:
• clinical trial management and clinical monitoring
• regulatory submissions
• biostatistics
• data management
• eSolutions
• medical writing
• medical safety
• quality assurance
• pharmacovigilance
• consulting services

With own offices in Germany, the UK and several EU countries, we conduct international clinical studies all over Europe and beyond.
We have experience in all phases and important medical indications, including oncology, cardiology, neurology, dermatology, and gastroenterology as well as in alternative therapies.
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Representative Services

Legal representation within the EU/EEA, for non-European sponsors conducting clinical studies with drugs or medical devices or seeking orphan drug designation / SME status application / marketing authorization in Europe.
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Pharmacovigilance

Vigilance services in support to pharmaceutical, biotech, and medical device companies obligations in managing risk-benefit profile of their products. Our services can be added to existing vigilance system of a client on a modular basis or comprise a stand-alone center of product vigilance on national, international or global level.
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