The European Medicines Agency (EMA) is advising marketing authorisation holders to submit type IA and type IAIN variations for 2019 no later than Friday 29 November 2019. This will enable EMA to acknowledge the validity of the submissions before the Agency’s closure between 23 December 2019 and 6 January 2020 and within the 30-day timeframe set out in Article 14 of Commission Regulation (EC) No 1234/2008.
Marketing authorisation holders planning to report Brexit-related Type IA/IAIN variations in December 2019 will receive the acknowledgment of the validity of the submissions within 30 days as per the usual procedure.
Marketing authorisation holders are advised to submit any type IB variations or groupings of type IBs and type IAs by 6 December 2019 for a start of procedure in 2019. For submissions received on or after 9 December 2019, the procedure may not start until January 2020.
For procedural or regulatory queries related to these procedures for human medicines, marketing authorisation holders can send an email to: email@example.com or firstname.lastname@example.org.
For veterinary medicines, marketing authorisation holders are advised to contact the vet applications team in advance of an upcoming submission at the following e-mail address: email@example.com.
Type IAIN and IA variations have no impact on the quality, safety or efficacy of the medicine. Type IAIN variations must be notified to the national competent authority or EMA immediately following implementation in order to ensure the continuous supervision of the medicine. Type IA variations do not require immediate notification and should be notified to the national competent authority or EMA within 12 months of implementation, or earlier in certain cases.
Type IB variations must be notified to the national competent authority or EMA before implementation, but do not require a formal approval. Upon acknowledgement of receipt of a valid notification, the marketing authorisation holder must wait for a period of 30 days to ensure that the notification is deemed acceptable by the national competent authority or EMA before implementing the change.