| PHUSE EU |
2024 |
Development of USDM through translation of human-readable protocols |
Stijn Rogiers |
source presentation source |
6 |
| PHUSE EU |
2023 |
Standardisation in a fast growing environment; MDR, EDC and other abbreviations |
Louella Schoemacher |
source presentation source |
6 |
| PHUSE EU |
2022 |
Maturing standardisation; the switch from spreadsheet-based standards to an MDR |
Louella Schoemacher |
source presentation source |
5 |
| PHUSE EU |
2022 |
Scaling within a Fast-moving Biotech Company. Key Learnings for Leaders and Innovators in Our Life Sciences Industry |
Stijn Rogiers |
source presentation source |
11 |
| PHUSE EU |
2020 |
Preparing for FDA and PMDA Submission Simultaneously - What to Leverage, How to Deal with the Differences Efficiently [presentation] |
|
source video |
22 |
| PHUSE EU |
2018 |
Cost-Benefit Analysis of Using CDISC Standards in Trial Set-up |
|
source |
9 |
| PHUSE EU |
2013 |
An Integrated Platform for Standards Management and Study Conduct - Managing Efficiently your Standards [presentation] |
Ine Felsenstein |
source |
29 |