The 3rd Annual Medical Device Regulatory and Quality Summit 2018, which will be held at Holiday Inn Delhi International Airport on August 9-10, 2018, will be reviewing the evolving regulations, their impact on the industry as well as take an in depth look into areas of quality control and assurance. It will be looking at specifications in the evolving regulations to create a strong and compliant framework within an organization The years 2017 and 2018 have been important for the medical device industry. The Finance Minister Arun Jaitley had declared that the government would formulate new norms, ‘harmonized with international rules’, for the medical devices sector as this would attract more foreign investment and reduce prices of medical devices. The rules framed around the guidelines of the Global Harmonization Task force (GHTF) ensure that the Indian norms governing medical devices are on par with those in vogue globally.
Medical devices, henceforth, both produced and imported, will conform to the best international practices of manufacturing, ensuring the prevalence of quality products in India. Since the industry is growing at a rapid pace, there is a need for clarity on regulations, export and import guidelines for the Industry. Following the success of Medical Device Regulatory Summit in 2016 and 2017, The 3rd Annual Medical Device Regulatory and Quality Summit will create a platform for regulators, industry stalwarts to come under one roof to discuss and share ideas that would not only benefit their organisations, but at large the industry as well. To participate in the 3rd Annual Medical Device Regulatory and Quality Summit 2018 and stay updated with the latest regulations to be implemented in the industry, register at www.meddeviceregulatorysummit.com
Source : www.pharmabiz.com
Published on: August 1, 2018