Regulatory Puzzle

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Across
  1. 3. The UK-wide medicines licensing agreement effective from January 1, 2025.
  2. 4. The electronic version of medicine information, including SmPC, leaflet, and labeling. (3 letters)
  3. 6. ___ country’s regulatory agency, is accepting the role of RMS for DCP and MRP submissions.
Down
  1. 1. The regulation that will govern all clinical trials in the EU from January 31, 2025, replacing the Clinical Trials Directive (CTD).
  2. 2. This EU system, becoming mandatory on February 2, 2025, allows MAHs and NCAs to report on medicine shortages, supply, demand, and availability. (4 letters)
  3. 5. The UK licensing and access pathway for faster patient access to innovative medicines.