EOM 1352: Fri 7 June 2024, 11:36

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Discovery Park: Wed 13 November 2024, 10:35
ramusmedical

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.

Catalyst: Fri 8 November 2024, 14:16
Biosynth: Wed 13 November 2024, 10:18