Personal Information
Entreprise/Lieu de travail
New York, NY United States
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
www.trialinteractive.com
À propos
For over 20 years, TransPerfect has helped life sciences companies conduct clinical development and commercialize products on a global scale. We bring that same level of expertise to our secure, web-based e-clinical solution, Trial Interactive. Trial Interactive enables the life sciences companies to streamline the execution and commercialization of global clinical trials and collaborate on partnerships while reducing administrative burdens. Our solutions are used by pharmaceutical, biotechnology, and medical device companies as well as CROs, IRBs/ECs and leading academic institutions involved in clinical development that stand up to the scrutiny of regulatory authorities globally.
Mots-clés
life sciences
investigative site
metadata
clinician reported outcomes
patient reported outcomes
pharmacovigilance system master file
marketing authorisation
european economic area
good pharmacovigilance practices
translation
global study
site management
pharmaceutical industry
clinical trial regulations
sponsors
clinical trial
eclinical
etmf
paperless
clinical trials
Tout plus
Présentations
(6)Personal Information
Entreprise/Lieu de travail
New York, NY United States
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
www.trialinteractive.com
À propos
For over 20 years, TransPerfect has helped life sciences companies conduct clinical development and commercialize products on a global scale. We bring that same level of expertise to our secure, web-based e-clinical solution, Trial Interactive. Trial Interactive enables the life sciences companies to streamline the execution and commercialization of global clinical trials and collaborate on partnerships while reducing administrative burdens. Our solutions are used by pharmaceutical, biotechnology, and medical device companies as well as CROs, IRBs/ECs and leading academic institutions involved in clinical development that stand up to the scrutiny of regulatory authorities globally.
Mots-clés
life sciences
investigative site
metadata
clinician reported outcomes
patient reported outcomes
pharmacovigilance system master file
marketing authorisation
european economic area
good pharmacovigilance practices
translation
global study
site management
pharmaceutical industry
clinical trial regulations
sponsors
clinical trial
eclinical
etmf
paperless
clinical trials
Tout plus