Regulatory update - EMA encourages companies to submit type I variations for 2017 by end of November
EMA to check validity of submissions by end 2017
The European Medicines Agency (EMA) is advising marketing authorisation holders to submit any type IAIN and Type IA variations for 2017 by Thursday 30 November. This will enable the Agency to acknowledge the validity of the submissions before the Agency's closure between 23 December 2017 and 2 January 2018 within the 30-day timeframe set out in Article 14 of Commission Regulation (EC) No 1234/2008.
Marketing authorisation holders are also advised to submit any Type IB variations or groupings of Type IBs and Type IAs for a start of procedure in 2017 by 8 December 2017. For submissions received on or after 11 December 2017, the procedure may not start until January 2018.
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 the EMA within 12 months of implementation, or earlier in certain cases.
Type IB variations must be notified to the national competent authority or the 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 the EMA before implementing the change.
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, the following e-mail address should be used: email@example.com.