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CITY OF PHOENIX POLICE DEPARTMENTREQUEST FOR INFORMATION RFI 19102 LAW ENFORCEMENT RECORDS MANAGEMENT SYSTEMPROCUREMENT OFFICER Gloria Elliot 251 W. Washington Street, 6th Floor Phoenix, AZ 85003

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Start by reviewing the request for information (RFI) document for PPD RMS.

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Who needs rfi for ppd rms?

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Organizations or individuals who are involved in or responsible for the procurement process of PPD RMS may require the RFI for PPD RMS. This may include project managers, procurement officers, or other relevant stakeholders who need to gather information about potential suppliers or solutions for PPD RMS.

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What is rfi for ppd rms?

RFI stands for Request for Information for Post-Market Surveillance. It is a document that gathers information related to the safety and performance of medical devices after they have been approved for marketing.

Who is required to file rfi for ppd rms?

Manufacturers of medical devices are required to file RFI for PPD RMS to provide updates on the safety and performance of their products.

How to fill out rfi for ppd rms?

RFI for PPD RMS can be filled out by providing detailed information about any adverse events, malfunctions, or recalls associated with the medical device. It is important to provide accurate and complete information in the RFI form.

What is the purpose of rfi for ppd rms?

The purpose of RFI for PPD RMS is to ensure the ongoing safety and performance of medical devices on the market by collecting and analyzing post-market surveillance data.

What information must be reported on rfi for ppd rms?

Information that must be reported on RFI for PPD RMS includes any adverse events, malfunctions, recalls, and other safety-related issues associated with the medical device.

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