Registry FAQs



Answer will be based on approved Administrative Order.
Please click create an account in the Login page.
If an account holder forgets the password or wants to reset the password, please click on the “Forgot your password” link on the Login page.
No. Once a study has been registered, it cannot be removed and remains publicly viewable.
Yes, the registrant is responsible for ensuring that the information provided in the registration record remains accurate and up-to-date.
Upon submission of the study for registration, the registry officer will then review the accomplished research form.

The study will either be rejected or approved. Rejected means there are other required information that the registrant needs to fill out.

Once all the required information are complete, the registry officer will approve the study. The registrant will be notified via email that the study has been registered.

The PHRR ID or Registry ID will be viewed when the registrant opens the title of the study using the registered account.
CLINICAL TRIAL
1. Public Title
2. Scientific Title
3. Registry ID
4. Secondary Identification Number
5. FDA Clinical Trial Reference Number
6. Project Description
7. Project Duration
8. Project Status
9. Implementing Agency (Primary Sponsor)
10. Cooperating Agency (Secondary Sponsor)
11. Funding Agency (Sources of Monetary or Material Support)
12. Contact for Public Queries (Name, Email, Phone Number, Postal Address)
13. Contact for Scientific Queries (Name, Email, Phone Number, Postal Address)
14. Investigating Team (Name, Expertise, Affiliation)
15. Project location and Institutional Ethics Review Board
16. Health Conditions or Problems Studied
17. Primary Outcomes
18. Key Secondary Outcomes
19. Recruitment Status
20. Countries of Recruitment
21. Research Classification
22. FDA Document Tracking Number
23. FDA/ERC Approval Date
24. Amendment Approval Date/Reasons
25. Key Inclusion and Exclusion Criteria
26. Study Type
27. Intervention Name
28. Intervention Description
29. Method of Allocation
30. Masking/Blinding
31. Masking Details
32. Assignment
33. Purpose
34. Phase
35. Target Sample Size (Philippines)
36. Actual Sample Size (Philippines)
37. Reason for Difference Between Target & Actual Sample Sizes
38. Date of First Enrollment
39. Research Utilization

NON-CLINICAL STUDIES
1. Public Title
2. Scientific Title
3. Registry ID
4. Project Description
5. NUHRA Details
6. Project Duration
7. Project Status
8. Implementing Agency (Primary Sponsor)
9. Cooperating Agency (Secondary Sponsor)
10. Funding Agency (Sources of Monetary or Material Support)
11. Contact for Public Queries (Name, Email, Phone Number, Postal Address)
12. Contact for Scientific Queries (Name, Email, Phone Number, Postal Address)
13. Investigating Team (Name, Expertise, Affiliation)
14. Primary Outcomes
15. Key Secondary Outcomes
16. Recruitment Status
17. Countries of Recruitment
18. Research Classification

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