Workshops

Our GCP Workshops provide a comprehensive training platform for ethics committees and consultants involved in clinical research. These one-day workshops cover a broad range of essential topics related to drug and device development, ensuring attendees are well-versed in the latest standards and regulations.

• Comprehensive Coverage: Topics include drug and device development guidelines, regulatory requirements, and the responsibilities of stakeholders.
• Ethics and Compliance: Focus on the roles of ethics committees and the application of ICMR and ICH-GCP guidelines for biomedical research.
• Updated Regulations: Discuss the New Clinical Trial Rules of 2019 to ensure compliance and up-to-date practices.

• Expert-Led Sessions: Led by seasoned academicians and industry experts, these workshops offer insights into the complexities of clinical research.
• Enhanced Understanding: Equip ethics committees and consultants with the knowledge to effectively oversee and consult on clinical trials.
• Regulatory Compliance: Ensure that participants are updated on the latest legal and ethical standards to guide their work in clinical research.

• The workshops are conducted by a distinguished faculty comprising experienced academicians and industry professionals who bring a wealth of knowledge and practical insights.