Good Clinical Practice is a process that incorporates established ethical and scientific quality standards for the design, conduct, recording and reporting of research involving human participants. Compliance with GCP assures the public that the rights, safety, and well-being of research participants are protected and respected, and are consistent with the principles enunciated in the Declaration of Helsinki and other internationally recognized ethical guidelines. Further, these ensure the integrity of clinical research data. The conduct of clinical research is complex and compounded by the need to involve stakeholders with a range of background all of whom must perform their tasks skillfully and efficiently. The course aims to strengthen knowledge and skills, and modify the attitude of researchers and health professionals in developing countries with regard to the management of research and apply Good Clinical Practices.
Principles of research ethics and GCP, and its application in research involving human participants Processes in product development, informed consent, safety & quality management and preparation of trial documents
Outputs expected/ Competencies to be acquired
Application of learning through assessment of their home laboratories using the provided checklist.
This training is designed for professionals who currently manage or work in a clinical setting with at least one (1) year of exposure, and those involved in clinical trials.
Fully accomplished and signed Application Form
Full payment two (2) weeks before the training
April 29-30, 2020
First day: 7:30 am – 5:00 pm
Second day: 8:00 am – 5:00 pm
Course Fee: To be finalized
Number of slots: 20
Course Point Person (CPP): Dr. Rosanna A. Ditangco
Contact Number: (02) 807-2628
E-mail Address: firstname.lastname@example.org
Secondary CPP (if available): Ms. Sheila Luz M. Punzalan
Note: For interested participants, kindly create an account and send your applications at RITM LDIS