In clinical studies, application for ethics committees and regulatory authority on a timely manner is significant in terms of study efficiency. Appropriate usage of document for studies ensures pure and rapid starts in projects with our local regulatory experience.
Our regulatory specialists have extensive clinical research expertise and experience. We always focus on providing high quality service on the needs and best interests of our clients.
Our local regulatory experience contains:
First Submission and document preparation of Ethics Committe
First Submission and document preparation of Regulatory Approval
Substantial Amendment Submission of clinical trails
Preparation of Notifications to Ethics Committe and Regulatory Authority