Sou Mieng Tran

Sou Mieng Tran

Vigilance Collaborations Specialist at Medicines and Healthcare products Regulatory Agency

United Kingdom

About me

Sou Mieng Tran is a Vigilance Collaborations Specialist at the Medicines and Healthcare products Regulatory Agency (MHRA), with a focus on advancing vigilance systems that support effective post-marketing surveillance of medicines and medical devices and enhance public health outcomes. Before moving to the UK, she worked at Medsafe, New Zealand’s medicines and medical devices regulator, specialising in pharmacovigilance. She remains a registered pharmacist in New Zealand and holds a Postgraduate Diploma in Health Policy.

Schedule

MHRA Case Study: The use of conditional questions to improve spontaneous reporting data: lessons learnt from a regulatory perspective

Sou Mieng Tran

Vigilance Collaborations Specialist at Medicines and Healthcare products Regulatory Agency

Data management & Analytics

Regulatory Compliance

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Data management & Analytics

Regulatory Compliance

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