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Training
We are committed to promoting excellence in clinical research through comprehensive training and capacity building programs.
We offer both basic and advanced training in Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and Good Clinical Laboratory Practice (GCLP). Our training programs are designed to ensure that all stakeholders have a thorough understanding of the relevant guidelines and regulations and are equipped with the knowledge and skills needed to conduct high-quality, compliant clinical research.
Target Audience
Clinical Research Professionals: Our training for clinical research professionals covers topics such as GCP, study design, protocol development, informed consent, subject recruitment and retention, data management, and safety reporting.
Drug Discovery and Development Scientists: our training focuses on the principles and practices of GLP and GMP, including quality assurance, documentation, and regulatory compliance.
Ethics Committees: Our training for ethics committees covers the ethical principles and guidelines governing clinical research, including the Declaration of Helsinki, the Belmont Report, and ICH GCP. We also provide training on the roles and responsibilities of ethics committees, including protocol review, informed consent, and ongoing study oversight.
Clinical Investigators: For clinical investigators, our training covers the principles and practices of GCP. We also provide training on specific therapeutic areas and study designs, as well as on the use of electronic data capture (EDC) systems and other clinical trial technologies.
Trial Site Staff: Our training for trial site staff covers the day-to-day operations of clinical trials, including subject screening and enrolment, data collection and documentation, investigational product management, and study closeout. We also provide training on the use of EDC systems and other clinical trial technologies, as well as on the principles and practices of GCP.