Course on Good Clinical Practices
Introduction
A good clinical practice is an international standard of ethical and scientific quality for designing, conducting, performing, monitoring, auditing, recording, analyzing and reporting clinical studies that involve the participation of human subjects. This model makes sure the reported data and results are credible and accurate, and that the rights, integrity and confidentiality of the study subjects are protected. (Definition taken from the INVIMA).
Duration
Eight (8) hours
Modality
100% Virtual
Certification
A certificate of participation in the course will be awarded upon completion of all lessons and completion of the final evaluation with a 90% score. Upon passing the evaluation, you will be able to download the certificate from the virtual platform.
Note:
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The course is available on our plaaorm 24 hours a day, 365 days a year.
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You can access the plaaorm, create an account with the data of the person who will be taking the course (Names, Surnames, I.D., others) and pay by credit card, debit card or cash via Baloto. As soon as the payment is confirmed, you will have access to the course.
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If you wish to pay by a deposit or any other method, please confirm by sending an e-mail to asistente.acic@gmail.com and aciccolombia2010@gmail.com.
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If you wish to pay by a deposit or any other method, please confirm by sending an e-mail to asistente.acic@gmail.com and aciccolombia2010@gmail.com.
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As soon as you complete the course and pass the evaluation, you will obtain a certificate that is valid for 3 years.
General Objectives
To provide conceptual, operational and ethical foundations in clinical research based on Good Clinical Practices, as well as the related national regulations in effect. This is in order to train staff on different disciplinary areas to execute and promote the development of clinical studies and concurrent activities on a national level.
Specific Objectives
- To review the conceptual bases of clinical research on an international and national level.
- To present the conceptual and operational bases of good clinical practices.
- To present the national regulations related to human research and clinical research.
- To disclose operational and ethical aspects of clinical research and the execution of clinical studies.
Virtual Platform
Access our platform where you will be able to purchase and start our virtual courses.