Domains targeting keyword clinical trial design

Strategic Consulting, Business Re-Engneering, Design and New Media, servicing the Healthcare, Financial Services, Legal and Corporate segments

Home Page for LifeTech Research

Professional Clinical Research Services including Project Management, Site Management, Quality Management and Quality Assurance

Clinical trial data collection and management software, services, CTMS, Safety, and Electronic data capture. Innovative leader in EDC to EHR Integration

Clinical trial management software - encrypted and safe. Design your own eCRF and use it to conduct surveys, data capture etc. Multiple site management etc.

IDDI provideS the best in class trial design, clinical data collection, standardization, analysis and reporting to your clinical trials.

PHASTAR is a specialist CRO offering statistical consultancy, clinical trial reporting and data management services by providing expert consultants and delivering in-house projects. Our number one priority is to ensure that the work we produce is of the highest quality: every project PHASTAR undertakes is supervised on methodology and utilises internal processes designed to ensure optimal quality. Services include production of clinical study reports including generating tables, figures and listings; study design and protocol writing; modelling and simulation; and advice on handling missing data across phase I to IV trials. Our headquarters is in Chiswick, London (UK) with additional offices across four continents. We partner with pharmaceutical and biotech companies globally..

International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. A standard for the design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate, and that the rights, integrity, and confidentiality of trial subjects are protected. Ethical and scientific quality standards for designing, conducting, recording and reporting trials that involve participation of human subjects to ensure that the RIGHTS, SAFETY and WELLBEING of the trial subjects are protected. Ensure the CREDIBILITY of clinical trial data. ICH GCP (E6): TABLE OF CONTENTS

Datavant organizes and structures the world's healthcare data for use in clinical trial decision-making. We combine patient-level clinical trial and real-world evidence to help pharma companies improve the design and interpretation of clinical trials.