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In this month's newsletter they shared recent guidance and key updates from the regulatory agencies:
- Food and Drug Association (FDA)
- European Medicines Agency (EMA)
- Medicines and Healthcare products Regulatory Agency (MHRA)
- European Commission (EC)
- World Health Organisation (WHO)
On 5 October, Boyds is hosting a free webinar on 'How to successfully operationalize real-world data collection alongside expanded access programs', for more info and how to sign up, click here.
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