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This forum has 16 topics, 50 replies, and was last updated 2 weeks, 4 days ago by Anonymous.

Viewing 15 topics - 1 through 15 (of 16 total)

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- CE-marked requirements for product to be used clinical investigation
- 1
- By Anonymous
- Out of country sourcing
- 2
- By Anonymous
- Package Insert
- 2
- By Anonymous
- Grace period for label changes
- 9
- By Anonymous
- Seeking examples of finished product release documents
- 3
- By Anonymous
- EU guideline on shipping and temp monitoring (536/2014)
- 8
- By Josh Anderson
- Regulatory release of IMP
- 6
- By Amy Thompson
- Comparator references in INDs
- 2
- By Anonymous
- IMP Accountability in IRT & Returns/Destruction @ site
- 7
- By Marla Cordova
- Virtual Finished CT Material Retention Samples
- 3
- By Anonymous
- Minimum Shelf Life Requirements for Importation to Asia-Pac
- 2
- By Anonymous
- Keeping Up With Changing Regulations
- 5
- By Anonymous
- COA vs COC
- 2
- By Anonymous
- New GCSG Global Regulatory Team
- 8
- By Philippe Van der Hofstadt
- Anti Microbial Resistance
- 4
- By Sue Lee

Viewing 15 topics - 1 through 15 (of 16 total)

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