Join the community - networking, discussion and more. Open to all.
More informationCould you write an interesting article for the RQA community?
More information5th July 2022
EMA
Call for companies to register their Industry Single Point of Contact (i-SPOC) on supply and availability.
Marketing authorisation holders (MAHs) can now register their Industry Single Point of Contact (i-SPOC) who will inform EMA about the supply and availability of critical medicines identified in the context of a ‘public health emergency’ or a ‘major event’ .
Regulation (EU) 2022/123 reinforces EMA’s role in crisis preparedness, including the monitoring and management of medicine shortages that may lead to a crisis and, during a public health emergency or a major event, with the reporting of shortages, information on supply and demand, and coordinating responses of EU countries to shortages of critical medicines. All pharmaceutical companies with a centrally- or nationally-authorised medicinal product in the EU are required to register a single point of contact.
The i-SPOC will facilitate rapid communication between EMA and MAHs to detect, report, and prevent or manage supply and availability issues of medicines included in a list of critical medicines for a ‘public health emergency’ or a ‘major event’. The Agency recently published the first list of critical medicines for the management of the COVID-19 pandemic.
Registration of an i-SPOC is a two-step process which may take up to 5-10 working days. EMA has updated the IRIS user guide and published a video demo to support companies with the registration process.
Companies must register their i-SPOC in EMA’s IRIS online platform by 2 September 2022.