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Good People Working on Good Projects with Good Process

Clinical Research



Prepare

Assess feasibility, review literature, and create budgets, protocols and essential documents

Initiate
Train personnel, submit FDA & IRB documents, register trials and adhere to timelines

Conduct
Monitor trials, manage site staff, collect data, analyze and report relevant information

Close Out
Close site, compile documents and create comprehensive reports

Case Study 1: Clinical Evaluation Report (CER)

Case Study 2: Risk Based Monitoring

Case Study 3: Clinical Trial Management

Regulatory Affairs >