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- Processing Of Follow-Up SAE (Event Is Still Ongoing)
  Started by: max in: Pharmacovigilance (PV)
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- 1
- 3 years, 5 months ago
  max
- ICSR Submissions
  Started by: max in: Pharmacovigilance (PV)
- 0
- 1
- 3 years, 5 months ago
  max
- SUSAR Submissions Using ICSR And Uploading XML Into EVWEB
  Started by: max in: Pharmacovigilance (PV)
- 0
- 1
- 3 years, 5 months ago
  max
- Experiences Of Self Monitoring By Sites?
  Started by: max in: Risk Based Monitoring
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- 1
- 3 years, 5 months ago
  max
- Experiences Of Requesting Remote Monitoring Of Sites?
  Started by: max in: Risk Based Monitoring
- 0
- 1
- 3 years, 5 months ago
  max
- Delegation Of Sponsorship Responsibilties
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
  max
- Preparing For Implementaion Of New CT Regulation
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
  max
- End Of Trial Reporting – Experience Of Using EudraCT
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
  max
- Experience Of Uploading Onto EudraCT Using Xml Files.
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
  max
- Template For IB For A Medical Device
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
  max
- Over-Encapsulation Of Hormones
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
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- Defining End Of Trial For Trials With Samples Being Analysed
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
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- GDPR And CVs Held In The TMF
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
  max
- GDPR – Transparency Obligations For Data Processors
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
  max
- ***GDPR Update*** Extra Resources Re The Lawful Basis For Processing Data
  Started by: max in: Regulation & Governance
- 0
- 1
- 3 years, 5 months ago
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Viewing 15 topics - 271 through 285 (of 442 total)

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