Peru - NIS Training

Course Details

This training session describes the regulatory requirements and operational considerations when running non-interventional studies (NIS) in Peru.

Topics covered:

  • Regulatory Definitions
  • Regulatory Classification Decision Tree
  • Regulatory Approvals
  • Study Start-Up Roadmap
  • Study Conduct Considerations

What you get with your subscription:

  • Narrated training session
  • PDF of the training slides
  • PDF of the training slide notes

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EU MDR Clinical Investigation Roadmaps and Detailed Requirements
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NIS Training Modules
EU MDR Clinical Investigation Roadmaps and Detailed Requirements
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NIS Training Modules
EU MDR Clinical Investigation Roadmaps and Detailed Requirements
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Billed MonthlyBilled Annually
Save money with an annual plan
Academic Pro
Monthly
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£1801800
Single Seat License
Ideal for Small Research Projects
50% Compared to Commercial Membership
Single Seat Licence
Monthly RWR Regulatory Updates
Country-Specific NIS Regulatory Requirements
NIS Training Modules
EU MDR Clinical Investigation Roadmaps and Detailed Requirements
Cancel Any Time
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£3603600
Up to 5 Seat License
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Monthly RWR Regulatory Updates
Country-Specific NIS Regulatory Requirements
NIS Training Modules
EU MDR Clinical Investigation Roadmaps and Detailed Requirements
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Monthly RWR Regulatory Updates
Country-Specific NIS Regulatory Requirements
EU MDR Clinical Investigation Roadmaps and Detailed Requirements
Priority Support
Personalised Onboarding
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