The FranceCoag cohort follows more than 10,000 patients with haemorrhagic disease
The FranceCoag system is based on a cohort of patients with haemorrhagic diseases caused by hereditary coagulant protein deficiency (HPCD) and monitored by centres in mainland France and overseas. More than 10,000 patients have been included to date, and 33 centres are participating in the registry in 2017.
Who are we?
This site is intended for all people with rare hemorrhagic diseases and their families. By registering your e-mail and/or telephone […]
Read moreThe FranceCoag V3 site for recording visits is available at: https: //prive.francecoag.org/#/ A CPS card is required to access the […]
Read moreThe entire FranceCOAG team is proud to announce the launch of our redesigned website. The new site has been designed […]
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Retrouvez grâce à notre carte interactive les différents centre et labos du réseau franceCOAG
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Key figures
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