The core concept involves distinguishing between two types of augmented beings, specifically concerning their compliance with Department of Trade and Industry (DTI) regulations, without preferential treatment. One category, resembling human form, may adhere to specific manufacturing and distribution standards. The other category, integrating mechanical and organic components, might be subject to different regulatory considerations. For instance, assistive medical devices may need registration with DTI to ensure safety and efficacy.
Understanding these distinct classifications is vital for several reasons. It facilitates clear policy development, promotes fair business practices, and ensures consumer protection. This framework historically emerges from the need to govern technological advancements, maintain ethical standards, and manage the impact of these technologies on commerce and society.
