From protocol development to sourcing the most qualified and cost effective Contract Research Organization (CRO), we help our clients to complete the entire process to get their clinical trials started. We have a wide range of experience designing and facilitating double-blind, placebo-controlled trials and provide the following services:
- Clinical research strategy development
- Protocol development and/or review
- Identification of suitable Contract Research Organizations (CROs)
- Clinical trial applications
- Feasibility assessments
- Regulatory applications and product approvals
- Health claim strategy and substantiation