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.” - ICH-GCP E6R3 Section 9.3

Clinical trials are crucial for testing the safety and efficacy of new treatments and medical interventions.


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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.”  - 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. 


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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.

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