Current Edition

Comparison and Compilation of RA and QA Requirements for Marketing Authorisation of Medical Devices: India, Singapore and Saudi Arabia

In order to market any medical device, marketing authorisation from a regulatory authority is required. The process of gaining authorisation is complex and multistep, and requires review of information by competent authorities. Dr Balamuralidhara V et al. from JSS School of Pharmacy, compare the marketing authorisation systems for medical device in emerging markets, i.e. India, Singapore and Saudi Arabia.