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  • REQUEST SUBMITTED

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    Date: 2021-01-14 13:39:19.400809

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    Date: 2021-01-14 16:18:30.155106

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    Date: 2021-01-26 13:03:30.524400

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Guidelines for Clinical Research Center

Requested from DOH by M. Dagohoy at 01:39 PM on Jan 14, 2021.
Purpose: Architectural search and development
Date of Coverage: 01/07/2007 - 01/07/2021
Tracking no: #DOH-727866047285

Dagohoy 01:39 PM, Jan 14, 2021 

Good Day! I would like to ask the following:

Is there any Architectural Planning Guidelines or minimum standards and laws about constructing a specialized clinical research center?

Receiving Officer 04:18 PM, Jan 14, 2021 

January 14, 2021

Dear Michelle Kate,

Thank you for your request dated Jan 14, 2021 under Executive Order No. 2 (s. 2016) on Freedom of Information in the Executive Branch, for Guidelines for Clinical Research Center.

We received your request on Jan 14, 2021 and will respond on or before Feb 04, 2021 01:39:19 PM, in accordance with the Executive Order's implementing rules and regulations.

Should you have any questions regarding your request, kindly contact me using the reply function on the eFOI portal at https://www.foi.gov.ph/requests/aglzfmVmb2ktcGhyHQsSB0NvbnRlbnQiEERPSC03Mjc4NjYwNDcyODUM, for request with ticket number #DOH-727866047285.

Thank you.

Respectfully,

FOI Receiving Officer

10:04 AM, Jan 22, 2021 

Hi Michelle Kate Dagohoy

Please be informed that your request has been endorsed to the Food and Drug Administration for action. Kindly await for their response, thank you


January 26, 2021

Dear Michelle Kate Dagohoy,

Greetings!

Thank you for your request dated Jan 14, 2021 01:39:19 PM under Executive Order No. 2 (s. 2016) on Freedom of Information in the Executive Branch.

Your request

You asked for Guidelines for Clinical Research Center.

Response to your request

While our aim is to provide information whenever possible, in this instance this Office does not have [some of]* the information you have requested. Please be advised that the Food and Drug Administration (FDA) have standards and policies for the approval, conduct and monitoring of clinical trials in the Philippines.  The FDA does not have standards or regulations about construction of clinical research center. 

May we suggest that you inquire with the Philippine Council for Health Research (PCHRD) under the Department of Science and Technology (DOST) regarding her concern.  

For further assistance you may review the FAQ section of the eFOI site: https://foi.gov.ph/help.

Your right to request a review

If you are unhappy with this response to your FOI request, you may ask us to carry out an internal review of the response by writing to Undersecretary Lilibeth C. David, Chair of Data Governance Oversight Committee/ DOH Central Appeals and Review Committee, at foi@doh.gov.ph. Your review request should explain why you are dissatisfied with this response, and should be made within 15 calendar days from the date when you received this letter. We will complete the review and tell you the result within 30 calendar days from the date when we receive your review request.

If you are not satisfied with the result of the review, you then have the right to appeal to the Office of the President under Administrative Order No. 22 (s. 2011).

Thank you.

Respectfully,
FOI Officer

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