What aspect does the MHRA primarily focus on?

The focus of the MHRA (Medicines and Healthcare products Regulatory Agency) is on the safety and efficacy of medical devices and medicines. This agency plays a crucial role in ensuring that both pharmaceutical products and medical devices meet rigorous standards before they can be made available to the public. The MHRA conducts evaluations and inspections to assess the quality, safety, and performance of these products. By regulating clinical trials, monitoring adverse effects, and supporting innovation in medical technology, the MHRA ensures that patients receive effective and safe treatments.

Healthcare accessibility pertains to the ability of individuals to obtain necessary healthcare services, while COSHH regulations (Control of Substances Hazardous to Health) deal with workplace safety regarding harmful substances and are not the main focus of the MHRA. Additionally, practitioner licensing involves the regulation of healthcare professional qualifications and is managed by separate bodies rather than the MHRA. Therefore, the emphasis on the safety and efficacy of medical devices and medicines distinctly aligns with the core mission of the MHRA.