International-level training based on ICH E6(R3) standards and accredited by TransCelerate
Good Clinical Practice
An international standard ensuring the ethical conduct of clinical trials and reliability of data
Aimed at protecting the rights, safety, and well-being of participants, and ensuring scientific accuracy and global recognition of results
Voluntary informed consent and respect for human dignity
Comprehensive protocol development considering both scientific and ethical standards
Accurate and reliable data reporting at every stage of a study
Conducts the study and ensures participant safety
Develops the protocol and provides resources for the study
Oversees compliance with the protocol and GCP standards
Protects participant rights and well-being
Accredited by
TransCelerate Biopharma Inc.
and updated to ICH E6(R3)
International GCP training consultant
For investigators, monitors, coordinators, and professionals in clinical research