Last Updated on November 1, 2024 by The Health Master
ICDRA
The 19th International Conference of Drug Regulatory Authorities (ICDRA) concluded its second day in New Delhi, India.
This global gathering brought together regulatory experts from around the world to discuss critical issues related to drug safety, quality, and access.
Hosted by the Central Drugs Standard Control Organization (CDSCO), the conference provided a platform for policymakers, health officials, and industry representatives to share knowledge, best practices, and challenges in the field of drug regulation.
Key Themes and Discussions
The ICDRA workshop delved into a wide range of topics, including:
- Regulatory Frameworks: Participants explored the regulatory frameworks and practices of various agencies worldwide, aiming to foster collaboration and harmonization.
- Quality Issues: The conference addressed concerns related to the quality of pharmaceutical products, including substandard and falsified medicines, and discussed strategies to ensure their safety and efficacy.
- Access to Medical Products: Delegates explored ways to improve access to essential medicines, particularly in underserved regions, by addressing issues such as affordability and availability.
- Regulatory Collaboration: The ICDRA emphasized the importance of international cooperation and collaboration among regulatory authorities to enhance global drug safety and efficacy.
- New Technologies: The conference also discussed the regulation of emerging technologies and novel drug delivery systems.
Key Highlights from the Workshop
- Facilitated Product Introduction Pathways: Experts discussed the impact of streamlined pathways for introducing new drugs to the market, focusing on their potential to improve access to essential medicines.
- Pharmaceutical Starting Materials: Participants shared experiences and best practices for ensuring the quality of pharmaceutical starting materials, which play a crucial role in drug manufacturing.
- Advanced Therapy Medicinal Products: The conference explored regulatory frameworks for advanced therapies, such as gene and cell therapies, and discussed challenges in their development and approval.
- Reducing Reliance on Animal Studies: Experts discussed the potential to reduce the use of animals in drug development and testing, exploring alternative methods and approaches.
- Improving Access to Medical Devices: The workshop focused on strategies to improve access to medical devices, including in vitro diagnostics (IVDs), through prequalification and reliance mechanisms.
In conclusion, the 19th ICDRA provided a valuable platform for global regulatory experts to exchange ideas, share experiences, and address pressing challenges in the field of drug regulation.
The conference’s focus on drug safety, quality, and access is essential for protecting public health and ensuring the availability of safe and effective medicines worldwide.
As the regulatory landscape continues to evolve, the ICDRA will remain a vital forum for fostering collaboration and driving progress in this critical area.
Disclaimer: This article contains information derived from the source mentioned below. Our team utilized an AI language model to rewrite and present the news or article in a unique format.
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