ICTA PM
@international_clinical_trial_association
Fontaine les Dijonhttp://www.icta.fr Pharmaceutical ManufacturingOverview
About ICTA PM
ICTA is an international privately-owned CRO with 40 years of experience in clinical R&D, pharmaco-epidemiology and Early and Compassionate programs for traditional and advanced therapies (including biologics cell and gene products), diagnostics and medical devices with over 1,000 Clinical Projects.
ICTAโs international operations in Western/Eastern Europe and North America provide full clinical research or โa la carteโ services in traditional and adaptive clinical trials from Early Phase to Late Phase across a broad range of therapeutic areas.
Additionally, ICTAโs consulting unit provides the pharmaceutical, medical device and biotech industries with strategic advice at every stage of your clinical developments.
Our full-services offering :
- ๐๐ฒ๐๐ถ๐ด๐ป: from drafting essential study documents to overseeing extensive medical writing programs
- ๐ฅ๐ฒ๐ด๐๐น๐ฎ๐๐ผ๐ฟ๐ ๐ฎ๐ณ๐ณ๐ฎ๐ถ๐ฟ๐: helping you anticipate challenges, overcome obstacles, and chart a clear, compliant path forward
- ๐ฃ๐ฟ๐ผ๐ท๐ฒ๐ฐ๐ ๐บ๐ฎ๐ป๐ฎ๐ด๐ฒ๐บ๐ฒ๐ป๐: we ensure seamless execution across every phase of your clinical study
- ๐ฆ๐ถ๐๐ฒ ๐ฆ๐๐ฝ๐ฝ๐ผ๐ฟ๐: our Clinical Research Assistants offer you their knowledge of local investigational structures to give you cost effective solutions
- ๐ฅ๐ถ๐๐ธ-๐ฏ๐ฎ๐๐ฒ๐ฑ ๐บ๐ผ๐ป๐ถ๐๐ผ๐ฟ๐ถ๐ป๐ด: improve data quality, ensure study continuity and reduce site burden.
- ๐ฃ๐ต๐ฎ๐ฟ๐บ๐ฎ๐ฐ๐ผ ๐ฎ๐ป๐ฑ ๐บ๐ฎ๐๐ฒ๐ฟ๐ถ๐ผ๐๐ถ๐ด๐ถ๐น๐ฎ๐ป๐ฐ๐ฒ: a wide range of safety services for your clinical research projects
- ๐๐ฎ๐๐ฎ ๐บ๐ฎ๐ป๐ฎ๐ด๐ฒ๐บ๐ฒ๐ป๐: from CRF design to final database lock, adapted to the context of each study
- ๐๐ถ๐ผ๐๐๐ฎ๐๐ถ๐๐๐ถ๐ฐ๐: ICTA biometry services to generate high-quality and reliable data for informed decision making.
- ๐ ๐ฒ๐ฑ๐ถ๐ฐ๐ฎ๐น ๐ช๐ฟ๐ถ๐๐ถ๐ป๐ด: flexible medical writing solutions to support your clinical program needs
Contact us by using the form on our website ๐
ICTAโs international operations in Western/Eastern Europe and North America provide full clinical research or โa la carteโ services in traditional and adaptive clinical trials from Early Phase to Late Phase across a broad range of therapeutic areas.
Additionally, ICTAโs consulting unit provides the pharmaceutical, medical device and biotech industries with strategic advice at every stage of your clinical developments.
Our full-services offering :
- ๐๐ฒ๐๐ถ๐ด๐ป: from drafting essential study documents to overseeing extensive medical writing programs
- ๐ฅ๐ฒ๐ด๐๐น๐ฎ๐๐ผ๐ฟ๐ ๐ฎ๐ณ๐ณ๐ฎ๐ถ๐ฟ๐: helping you anticipate challenges, overcome obstacles, and chart a clear, compliant path forward
- ๐ฃ๐ฟ๐ผ๐ท๐ฒ๐ฐ๐ ๐บ๐ฎ๐ป๐ฎ๐ด๐ฒ๐บ๐ฒ๐ป๐: we ensure seamless execution across every phase of your clinical study
- ๐ฆ๐ถ๐๐ฒ ๐ฆ๐๐ฝ๐ฝ๐ผ๐ฟ๐: our Clinical Research Assistants offer you their knowledge of local investigational structures to give you cost effective solutions
- ๐ฅ๐ถ๐๐ธ-๐ฏ๐ฎ๐๐ฒ๐ฑ ๐บ๐ผ๐ป๐ถ๐๐ผ๐ฟ๐ถ๐ป๐ด: improve data quality, ensure study continuity and reduce site burden.
- ๐ฃ๐ต๐ฎ๐ฟ๐บ๐ฎ๐ฐ๐ผ ๐ฎ๐ป๐ฑ ๐บ๐ฎ๐๐ฒ๐ฟ๐ถ๐ผ๐๐ถ๐ด๐ถ๐น๐ฎ๐ป๐ฐ๐ฒ: a wide range of safety services for your clinical research projects
- ๐๐ฎ๐๐ฎ ๐บ๐ฎ๐ป๐ฎ๐ด๐ฒ๐บ๐ฒ๐ป๐: from CRF design to final database lock, adapted to the context of each study
- ๐๐ถ๐ผ๐๐๐ฎ๐๐ถ๐๐๐ถ๐ฐ๐: ICTA biometry services to generate high-quality and reliable data for informed decision making.
- ๐ ๐ฒ๐ฑ๐ถ๐ฐ๐ฎ๐น ๐ช๐ฟ๐ถ๐๐ถ๐ป๐ด: flexible medical writing solutions to support your clinical program needs
Contact us by using the form on our website ๐