Small pharmaceutical companies typically rely on Clinical Research Organizations (CROs) to provide specialized expertise, infrastructure, and operational support to help them successfully conduct clinical trial. Their expectations can be summarized as follows:
1. Expertise and Guidance
- Regulatory Knowledge: CROs should have deep knowledge of the regulatory landscape in the regions where the trials will be conducted, ensuring compliance with local and international standards.
- Trial Design Expertise: Assistance with designing efficient and scientifically robust protocols, and practical feasibility.
- Therapeutic Area Expertise: Familiarity with the specific therapeutic area or indication being studied.