Clinical research facilitates medical advancements through a systematic process of generating knowledge to better understand human diseases, validate diagnoses and treatments, and improve overall health outcomes.
Our mission
The field of clinical research is extensive, with much to explore and learn. The purpose of this project is to guide and assist those who are interested in navigating the complex environment that is clinical research by curating and publishing a collection of resources on a wide array of topics, minimizing personal opinions, interpretations, and bias, including:
- Clinical trial conduct: from design and planning to data analysis and reporting
- Data collection and analysis: methodologies and tools used in gathering and interpreting data
- Regulatory compliance: regulations and guidelines that ensure the safety and ethics of clinical research, including the roles of organizations like the FDA and EMA
- Ethical considerations: framework that guides researchers in ensuring the welfare and rights of study participants
- Patient recruitment: process of identifying and enrolling eligible participants for clinical trials
- Clinical research careers: career opportunities in the clinical research field and the skills required to excel in this dynamic industry
This collection aims to serve as a foundation for deeper understanding and knowledge acquisition in the field of medical science, providing a reliable basis for further analysis, decision-making, and research.
Lists of published pages
Latest pages
Below you will find a list of the latest pages of this site:
- Clinical research regulations in the European Union
- Comparison of IRB and IEC requirements
- Artificial intelligence
- Certified copy
- 45 CFR 46
- Bias
- Clinical trial registry
- Well-being
- Vulnerable subjects
- Unexpected adverse drug reaction
- Trial site
- Subject identification code
- Plain language summary of study results
- Subject
- Sub-investigator
- Standard operating procedures
- Sponsor-investigator
- 21 CFR 312