BLOGS
Simplifying Trial Processes for Effective Operation
“Trial processes should be operationally feasible and avoid unnecessary complexity, procedures and data collection. Trial processes should support the key trial objectives.”
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ICH-GCP E6R3 Section 9.3
Clinical trials are crucial for testing the safety and efficacy of new treatments and medical interventions.
Safeguarding Trial Participants: The Role of IRB/IEC
“The purpose of an IRB/IEC is to safeguard the rights, safety and well-being of all trial participants.”
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ICH-GCP E6R3 Section 1.1.1
Clinical trials are pivotal in the progression of medical understanding and the enhancement of patient care. However, ensuring the ethical conduct of these trials is paramount.
Simplifying Trial Processes for Effective Operation
“Trial processes should be operationally feasible and avoid unnecessary complexity, procedures and data collection. Trial processes should support the key trial objectives.” - ICH-GCP E6R3 Section 9.3
Clinical trials are crucial for testing the safety and efficacy of new treatments and medical interventions.