Danielle Giroud’s Post

View profile for Danielle Giroud

CEO at MD-CLINICALS SA

It is with great pleasure that I announce a 96% positive voting on the FDIS ISO 14155:2020. I want to thank all WG members for their relentless support in making this happen. Last steps on track to bring out the final document in June 2020! Danielle Giroud

Jens Goetzke

Sr. Clinical Trial Manager

3y

Hi Danielle, maybe you remember me, we have been in touch via WMDO some years ago or a project I lead at Boston Scientific! Looking forward the new ISO 14155 revision. Is the plan still to have it published in June 2020?

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Eréndira Rodríguez

Director of Quality Assurance and Regulatory Affairs at Wellinq

3y
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Lennart Ivarsson, PhD

Clinical Operations Leader and Expert I 🌎Global Clinical Studies I 🎯Deliver on quality, time and budget I 🔹Mentoring I Strategy I Regulatory

3y

That is really great news! Congrats Danielle and the whole WG to the finalization of this KEY document!!

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Rita Herrenknecht

Strategic Clinical MedTech Consultant

3y

Great News Danielle!

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"Tommi" Trudy P.

FDA Alumni, President, Regulatory Consultants Group, Past Pres. PRCSQA.org, OCRA.org, Committees:FDAAA, SQA Communications-Publications, DiversityBC, QACS,

3y

Perseverance prevails. Terrific work

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Lars-Eric Ellow

Now retired - still experienced Life Science Seminar Organizer and Creator of Compliance Network.

3y

Good work Dainelle - well deserved weekend! ;-)

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Jon I. Bergsteinsson

💫 Fractional CMO & CRO | Founder | Advisor | Investor | Future of MedTech | SaaS | Blockchain | AI | MedTech | Regulatory | Clinical Trials | Clinical Data | Healthcare

3y

Very positive news!

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Joy Frestedt, PhD

Author | Speaker | Trainer | expanding reach and creating new roles to accelerate patient care successes

3y

Go team!

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Malcolm Applewhite, M.Sc

Medical Device QA and Regulatory Affairs Consultant

3y

Congratulations and great work!

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Mark Grumbridge CSci MTOPRA

Head of Clinical Investigations MHRA

3y

Well done Danielle !

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