Poor-quality medical devices are increasingly being sold in India, according to a recent report. The country’s Pharma Secretary has called for stronger testing of finished medical devices and a regulatory framework tailored specifically for the sector.
The report highlights concerns over the safety and efficacy of medical devices available in the market. Many of these products fail to meet international standards, posing risks to patients. The Pharma Secretary emphasized the need for more rigorous quality control measures to ensure that only safe and effective devices reach consumers.
Currently, the regulatory framework for medical devices in India is considered inadequate. The lack of standardized testing protocols has led to the proliferation of substandard products. Industry experts agree that a dedicated regulatory body could help streamline the approval process and improve oversight.
The call for reform comes amid growing awareness of the risks associated with low-quality medical devices. Stakeholders are urging the government to take immediate action to protect public health.
