Across
- 3. Substances, strengths, dosage form, etc.
- 4. Submit after approval
- 6. Chemicals, proteins, nucleic acids, etc.
- 7. EU's Master Data phase approach for IDMP Implementation
- 9. IDMP in 2022
Down
- 1. IDMP in 2021
- 2. Product name, clinical particulars, manufacturer, etc.
- 5. M of UoM (ISO 11240)
- 8. Number of IDMP standards