GCP Training as held on 7th and 8th December 2022
Good clinical practice guidelines and dimensions, IRB/EC, Investigator responsibilities, Human Subject Protection with Research Ethics, Documentation, Adverse events, Informed consent and confidentiality, Investigational product, Drug development process, Clinical trial monitoring, Audits and inspections, Standard Operating procedures, Clinical research steps, Practical training, Protocol Deviations and violations.
Training in Progress
Learning and growing together during the GCP training sessions
Acquiring valuable skills and knowledge through our GCP training sessions
Empowering our team with the tools they need to succeed through GCP training.
Simplifying drug development processes to the team by the Site pharmacist.
Advancing research capabilities through GCP training.
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