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Pages that link to "Regulated Clinical Research Information Management"
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The following pages link to Regulated Clinical Research Information Management:
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Laboratory Result-based Adverse Event Assessment Messaging Project (← links)
- Regulated Product Submissions (← links)
- Structured Product Labeling (← links)
- Study Design, Study Participation and Subject Data (← links)
- RPS Glossary (← links)
- Category:RPS Glossary (← links)
- NDA (← links)
- Clinical Trials Registration and Results (← links)
- Drug Stability Reporting (← links)
- Medical Product and Device Listing (← links)
- Periodic Reporting of Clinical Trial Laboratory Data, Release 2 (← links)
- RCRIM Working Group Meeting Agendas (← links)
- RCRIM Working Group Meeting Minutes (← links)
- RCRIM Vocabulary (← links)
- Annotated ECG (← links)
- BRIDG as DAM (← links)
- RPS Project Notes10112009 (← links)
- RPS Project Notes24112009 (← links)
- RPS Project Notes08122009 (← links)
- RPS Project Notes22122009 (← links)
- RPS R3 Project Scope Statement (← links)
- RPS Meeting Notes 01052010 (← links)
- RPS Meeting Notes 01262010 (← links)
- RPS Meeting Notes 02092010 (← links)
- Medical Product Information (includes Drugs, Devices, Biologics, Veterinary Products) (SPLr5) (← links)
- Medical Product Information (SPLr5) (← links)
- RPS Meeting Notes 08102010 (← links)
- Study Data XForms (← links)
- RCRIM Teleconference Minutes and Agendas (← links)
- RCRIM Electronic Voting (← links)
- RCRIM 2015 May Working Group Meeting Agendas (← links)
- Main Page (← links)
- AdverseEvent FHIR Resource Proposal (← links)
- Structured Product Labeling for Food and Dietary Supplements (SPLr8) (← links)
- Study FHIR Resource Proposal (← links)
- StudyParticipation FHIR Resource Proposal (← links)