Author: ARPA Editorial

  Priya Jayaraman, Ph D Chair of Clinical Trial Chapter (ARPA) Synergy between regulatory associates and clinical operations team Regulations play a key role right from the time when a product is conceived and even after it is placed in the market.  Throughout the product lifecycle, it is essential for a regulatory professional to interact…

[ARPA] Hi Mr Yoon, Thank you for supporting ARPA.   [ARPA] 1. What is the change about and when is it effective? [Mr Yoon] The “In-vitro Diagnostic Medical Devices Act”(IVD Act) went into effect as of May 1, 2020 with an aim to support prompter commercialization and R&D for the product category of in-vitro diagnostic…