|
No. |
Topic |
Summary |
Pages |
9437
| Influence of API properties on drug product | - | 58 |
9438
| Challenges in pharmaceutical development and technologies to deal with them | - | 41 |
9439
| PAT and QbD - an interdisciplinary system from Development to Production | - | 35 |
9440
| Integration of ICH Q8, Q9, Q10 elements and PAT into CMC documentation | - | 34 |
9441
| PAT challenges and possibilities from the authority point of view | - | 37 |
9442
| Process Development for Biotechnological Processes: Ensuring cGMP Compliance | - | 57 |
9443
| Regulatory Strategy for Biotechnology & Advanced Therapy Medicinal Products | - | 40 |
9444
| The EU Inspection System | - | 37 |
9445
| The Management of IMP supplies | - | 36 |
9446
| Scale-up and transfer of process and product - compliant and efficient | - | 46 |
