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DISCOVER

our Quality& credentials

Quality Management
at the very centre
of the Telemedicine Technologies corporate
strategy

ISO 9001:2015 certification
ISO 27001 HDS

Regulatory compliance:
21 CRF part 11 FDA

CDISC-ODM Certification

Information System Validation:
GAMP-5 methodology

National Qualiopi certification,
a new quality guarantee for
training providers in France

Some key figures that testify to our involvement and leadership in
the clinical research industry for over 20 years

64 +

countries
involved

20 000 +

investigational
center

2 million +

patients
in database

50 000 +

users
worlwide

97%

overall trainee
satisfaction rate

90+

monitored
servers

5 500+

projects

A LEADING POSITION AND
AN INTERNATIONAL DEPLOYMENT

64 +

countries
involved

20 000 +

investigational
Centres

3 million +

patients
in database

50 000 +

users
worlwide

telemedicine technologies earth

LATEST NEWSOUR NEWS >

telemedecine technologies news

Standards in Sync: Accelerating Medical Research – EUCROF Webinar

June 27, 2024

25 September 2024 from 4:00PM to 5:30PM (CEST) Webinar Overview It has been demonstrated that using standards from the start of clinical research studies (i.e. protocol and CRF development) can save significant time and resources and results in higher quality research. Unfortunately, it is not always clear how to select the appropriate standards for the […]

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telemedecine technologies news

Addressing Data Management Challenges With Automation

June 27, 2024

Applied Clinical Trials Online ACT: How can data management challenges be addressed? Specifically, is there any opportunity to address them with artificial intelligence (AI)? Lacroix: There is a lot of opportunity across the life cycle to assist with this and it’s interesting because historically it was always: we want to throw people at some of […]

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telemedecine technologies news

Why early market access planning is crucial in CGT commercial strategy

June 27, 2024

Fiercebiotech Experts recommend that CGT manufacturers proactively design a comprehensive market access strategy early in clinical development and commercial planning timelines, ideally more than three years prior to launch. This strategy should focus on addressing the nuanced market access challenges for such treatments, including but not limited to, distribution network design, tailored commercial site engagement, […]

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