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- [36] Best Practices for the Development, Scale-up, and Post-approval Change Control of IR and MR Dosage Forms in the Current Quality-by-Design Paradigm AAPS PHARMSCITECH, 2014, 15 (03): : 665 - 693
- [37] Best Practices for the Development, Scale-up, and Post-approval Change Control of IR and MR Dosage Forms in the Current Quality-by-Design Paradigm AAPS PharmSciTech, 2014, 15 : 665 - 693
- [40] Path Forward to Optimise Post-approval Change Management and Facilitate Continuous Supply of Medicines and Vaccines of High Quality WorldwideJoint Position from EFPIA, IFPMA and Vaccines Europe Therapeutic Innovation & Regulatory Science, 2023, 57 : 7 - 11