eCTD in Limelight. HPRA to Make Electronic Submissions Mandatory

Ever since the electronic submissions initiated, there are growing instances that both health authorities and drug manufacturers are being benefitted. Intended to make it the same situation for human medicines manufacturers in its jurisdiction, the Health Products Regulatory Authority – HPRA (formerly known as Irish Medicines Board [IMB]) is now in plans to implement the eCTD (electronic common technical document) format as mandatory towards the end of 2018.

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