Program and Protocol Design Services
Don’t wonder if it's right. Be sure it's right.
The design of your study protocol plays a critical role in ensuring scientific rigour, ethical conduct, and results driven success for your clinical trial. It takes a substantial team with diverse expertise to complete the program and protocol design process.
At MUCTC, our team of experts can help you design protocols that produce reliable, valid, and generalisable results.
Engage with our team to help you optimise your program and protocol design. We can help you ensure it’s viable and efficient so you attain reliable and valid scientific results.
CORE SERVICES
- Protocol design and development
- Investigational Brochure (IB) design and development
- Essential document preparation and management
- Human Research Ethics Committee (HREC) and participant Information and Consent Form (PICF) development
- Case Report Form (CRF) and database development
- Resource optimisation
- Regulatory compliance
- Risk management plan
- Scientific validity.
