The medical device industry in India has poor supervision and regulatory approaches to provide CE certifications and monitor, what is being sold in the Indian market.  India lacks control when it comes to selling medical devices in the Indian market, unlike FDA in the US, and CE in Europe, which require manufacturers to meet stringent standards.  The Indian market has been flooded with manufacturers who have fake CE mark certifications and positioning themselves in front of buyers and purchasing departments that lack the knowledge and tools to differentiate fake and authentic certificates. The burden of proof also lies on companies with legitimate...