[dsm_gradient_text gradient_text="ISO 17025, Laboratories, and AI: A New Era of Compliance and Innovation" _builder_version="4.27.0" _module_preset="default" header_font="Questrial|||on|||||" header_text_align="center" header_letter_spacing="5px"...
Product safety and security in global supply chains face significant challenges due to their complexity, including risks of contamination, counterfeiting, and regulatory disparities. Industries such as food, pharmaceuticals, and medical devices are particularly vulnerable. Addressing these issues presents opportunities for research in regulation, traceability systems, and supplier management strategies.
Explore the ethical challenges and risk management strategies in biomedical software design, emphasizing the importance of comprehensive frameworks like the Software Development Impact Statement (SoDIS) to safeguard patient safety, privacy, and equity in healthcare technology.
Good Manufacturing Practice (GMP) and Good Industrial Large Scale Practice (GLSP) are essential regulatory frameworks that ensure the quality, safety, and consistency of products in pharmaceutical, biotechnology, and food industries. By adhering to these practices, companies can minimize contamination risks, ensure regulatory compliance, and achieve excellence in large-scale manufacturing operations.