Regulatory Rapporteur April 2015
Volume 12 Issue 4
In This Issue
- FOCUS - Lifecycle management
- PLUS
- Conducting clinical trials in Jordan
- Health Canada: New legislation reviewed
- An interview with Dr Esther Werner, PEI
Please login to view member only articles. Non-members may download the public articles.
| Title | Download | Category | Size | File |
|---|---|---|---|---|
| Regulatory Rapporteur April 2015 | Members | Full Issue | 1MB | |
| A guide to the EU variation procedure from a quality viewpoint | Public | 75KB | ||
| Editorial: Strategies to enhance the lifecycle of your product | Public | 43KB | ||
| 8th EGA Pharmacovigilance Discussion Forum | Members | 84KB | ||
| Biosimilars Global Congress 2014 Europe | Members | 72KB | ||
| Green meadows, new pastures: Interview with Dr Esther Werner | Members | 76KB | ||
| Handling variation applications and lifecycle impacts within electronic submission formats | Members | 109KB | ||
| Harmonisation of variation requirements, categorisation and implementation: A global view | Members | 102KB | ||
| Maple Leaf News – Update from Canada | Members | 51KB | ||
| The evolving clinical research environment in Jordan | Members | 133KB |