itec services

From its beginnings in 1984, ITEC Services is one of the first French CRO (contract research organisation), privately owned, ISO certified, acting as a leading global CRO to manage : - Interventional studies - Minimal risks and constraints and non-interventional studies - Authorization for Temporary Use (ATU) - Recommendations for Temporary Use (RTU) - Secondary use of data thanks to Medico-administrative databases analysing Our Mission ITEC Services provides clinical trial and other research support services for the pharmaceutical, biotechnology, medical device industries, cosmetic companies and also serving government institutions, foundations, and universities in France, Europe and International. Our Added Value - Strong expertise and Clients recognition - Methodology and experience enable us to provide the highest level of services - Commitments to consistent quality and execution of clinical trials to assure: - Safety of patients - Integrity of data - Compliance with the applicable law, standard operating procedures, protocols, clients requirements and contracts - Solid and validated support systems and infrastructure - Quality System Management (QSM) has been certified ISO 9001 since 1997 - Information Security Management Systems (ISMS) has been compliant ISO 27001 since 2015 - Compliant systems with FDA (21 CFR Part 11) and EU recommendations in terms of safety and trial audits - Implication of the Direction and its Board in all projects - Easy access for all clients and partners

Research
,
Founded in unknown
51-200 employees

From its beginnings in 1984, ITEC Services is one of the first French CRO (contract research organisation), privately owned, ISO certified, acting as a leading global CRO to manage : - Interventional studies - Minimal risks and constraints and non-interventional studies - Authorization for Temporary Use (ATU) - Recommendations for Temporary Use (RTU) - Secondary use of data thanks to Medico-administrative databases analysing Our Mission ITEC Services provides clinical trial and other research support services for the pharmaceutical, biotechnology, medical device industries, cosmetic companies and also serving government institutions, foundations, and universities in France, Europe and International. Our Added Value - Strong expertise and Clients recognition - Methodology and experience enable us to provide the highest level of services - Commitments to consistent quality and execution of clinical trials to assure: - Safety of patients - Integrity of data - Compliance with the applicable law, standard operating procedures, protocols, clients requirements and contracts - Solid and validated support systems and infrastructure - Quality System Management (QSM) has been certified ISO 9001 since 1997 - Information Security Management Systems (ISMS) has been compliant ISO 27001 since 2015 - Compliant systems with FDA (21 CFR Part 11) and EU recommendations in terms of safety and trial audits - Implication of the Direction and its Board in all projects - Easy access for all clients and partners

Company Information

Industry
Research
Company Type
Privately Held
Founded
unknown
Employee Range
51-200
Revenue Range
Not available

Location

Address
3 avenue Georges Clemenceau CENON
City
Region
Postal Code
33150
Country
France

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