Norstella

Gemma

Learning Center

The Disclose Training Guides provide a detailed description of all Disclose features.

Disclose Training Guides

ERF to RRF AEs

How to Add Custom Compliance Authority?

How to import acquired studies into Disclose

How to convert a PDF to PDF/A format (acceptable by PRS)

Recommended to use FireFox browser to print large forms to PDF

How to set up user-managed credentials for Odata access

How to connect to the Disclose Analytics models using OData and Excel

Tracking Secondary Outcome Measure Disclosure

How to determine PRS's grace period for accepting Anticipated Study Dates which are in the past

How to submit a request for delayed results

How to create a Manual Compliance Event with Template assignment

How to Review Data in the New User Interface (v2.18.1 and above)

How to Approve Tasks in the New User Interface

How to create a new user and grant access

How to Sync Data from the RRF to the ERF

How to view PRS Reviewer Major (QA/QC) Comments

How to view form version history in the new user interface (V2.18.1 and above)

How to print in the New User Interface (V2.18.1 and Above)

How to preview data in ClinicalTrials.gov format in the new user interface (V2.18.1 and above)

How to use Global Search in New User Interface (V2.18.1 and Above)

How to view validation messages on ClinicalTrials.gov forms in the new user interface (V2.18.1 and above)

How to navigate between the new Interface and full application (V2.18.1 and Above)

How to compare ClinicalTrials.gov form versions in the new user interface (V2.18.1 and above)

How to comment on ClinicalTrials.gov Forms in the New User Interface (V2.18.1 and Above)

How to start a task or edit a date at the task level (v2.18 and above)

How to assign or add users at the task level (v2.18 and above)

How to send an email on demand (v2.18 and above)

How to change a workflow template after a study is created (v2.18 and above)

How to Identify Studies with QA Comments

How to Link Roles to Permissions

How to update Administration -> Codes

How to Submit Data to CTGOV

How to Store Sponsor info and CT.Gov Credentials

How to Add/Edit Product Information

How to Approve Data in Disclose

How to Review Data in Disclose

How to Subscribe to Reports

How to set Default and Required Roles

How to Download Reports

User Profile-How to Subscribe to E-Mail Notifications

How to add a Product

How to Receive Data Notifications

How to Compare Data

How to Copy Data from PRF to RRF

How to Download a Public Site Report from CTGOV

How to Import EU Results Data XML

How to Copy Roles and Assignments

How to Create a Study Manually

How to Manually Assess for Disclosure and Add Roles Automatically

How to Delete and Complete a Study

How to Edit and Validate a Form

How can I interpret Workflow Manager messages?

How to populate the Number Analyzed and Category per row for an Outcome Measure

How can I update the attachment type for an existing attachment?

Import Guidance Document

How to create Plain-Language Summary (PLS) Compliance Event with attachment (Version 2.18.3 and above)

What are Messages?

Using the Browse Tab in Disclose (Version 2.17 and above)

Did you know that you can Copy roles from one study to another (Version 2.18 and above)?

How to Start a Task or Edit a Date at the Task Level

How to Identify Data Syncing

How Tos

Compliance Rules

AGES (Austria) Assessment & Compliance Due Date Rules

ANZCTR (Australia and New Zealand) Assessment & Compliance Due Date Rules

ChiCTR (China) Assessment & Compliance Due Date Rules

ChinaDrugTrials.org.cn (China) Assessment & Compliance Due Date Rules

Company Compliance Due Date Rules

CRiS (Korea) Assessment & Compliance Due Date Rules

CTGOV (United States) Assessment & Compliance Due Date Rules

CTRI (India) Assessment & Compliance Due Date Rules

DRKS (Germany) Assessment & Compliance Due Date Rules

EU PAS ENCePP (EU) Assessment & Compliance Due Date Rules

GRLS (Russia) Assessment & Compliance Due Date Rules

HKU CTR (Hong Kong) Assessment & Compliance Due Date Rules

IRCT (Iran) Assessment & Compliance Due Date Rules

IRPMA PMS (Taiwan) Assessment & Compliance Due Date Rules

ISRCTN (UK) Assessment & Compliance Due Date Rules

JAPIC (Japan) Assessment & Compliance Due Date Rules

JPRN (Japan) Assessment & Compliance Due Date Rules

JRCT (Japan) Assessment & Compliance Due Date Rules

NMRR (Malaysia) Assessment & Compliance Due Date Rules

PharmNet.Bund (Germany) Assessment & Compliance Due Date Rules

PHRR (Phillippines) Assessment & Compliance Due Date Rules

ReBec (Brazil) Assessment & Compliance Due Date Rules

REEC (Spain) Assessment & Compliance Due Date Rules

RNEC (Portugal) Assessment & Compliance Due Date Rules

RNEC (Mexico) Assessment & Compliance Due Date Rules

RPCEC (Cuba) Assessment & Compliance Due Date Rules

SLCTR (Sri Lanka) Assessment & Compliance Due Date Rules

SUKL (Czech Republic) Assessment & Compliance Due Date Rules

TCTR (Thailand) Assessment & Compliance Due Date Rules

ToetsingOnline (Netherlands) Assessment & Compliance Due Date Rules

NTR (Netherlands) Assessment & Compliance Due Date Rules

PACTR (Africa) Assessment & Compliance Due Date Rules

PPB (Kenya) Assessment & Compliance Due Date Rules

REPEC (Peru) Assessment & Compliance Due Date Rules

SNCTP (Switzerland) Assessment & Compliance Due Date Rules

Global Rules

Find answers and get help from Intercom Support and Community Experts

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