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Phase
II-IV Studies at Synchron Research
 FIRST-INTO MAN STUDIES
FEASIBILITY STUDY
PROTOCOL DEVELOPMENT
SITE IDENTIFICATION
CLINICAL INVESTIGATOR
SELECTION
CLINICAL STUDY MONITORING
CLINICAL TRIAL CO-ORDINATION
CLINICAL TRIAL PROJECT
MANAGEMENT
INDEPENDENT ETHICS
COMMITTEE SUBMISSION
REGULATORY SUBMISSIONS
POST MARKETING SURVEILLANCE
Our GCP trained personnel are competent to carry out the above functions
which meet International standards. All project management activities
are carried out in compliance with ICH and GCP guidelines.
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Phase II-IV