# How to Prepare a Pre-Request for Designation (Pre-RFD): Guidance for Industry - FDA Guidance Document Source: https://www.globalkeysolutions.net/guidances/guidance-document/how-to-prepare-a-pre-request-for-designation-pre-rfd-guidance-for-industry/cc79c332-6e12-4bdf-8c0a-a8993430308a > FDA guidance document: How to Prepare a Pre-Request for Designation (Pre-RFD): Guidance for Industry. Issue date: February 14, 2018. Get complete insights and analysis. --- ## Details - Title: How to Prepare a Pre-Request for Designation (Pre-RFD): Guidance for Industry - Communication Type: Guidance Document - Product Type: devices - Office Name: Office of the Commissioner - Office URL: /offices/office-of-the-commissioner/79483979-9582-427f-ac3d-46c715811424 - Issue Date: 2018-02-14 - Comment Close Date: 2017-04-13 - Last Changed: 2020-01-21 - Docket Number: FDA-2017-D-0040 ## Related Documents - [Safety Assessment of Genome Editing in Human Gene Therapy Products Using Next-Generation Sequencing](https://www.globalkeysolutions.net/guidances/guidance-document/safety-assessment-of-genome-editing-in-human-gene-therapy-products-using-next-generation-sequencing/8bd86906-9b70-4e40-ae4a-dde0c1ea99ca) - [Expedited Programs for Regenerative Medicine Therapies for Serious Conditions: Draft Guidance for Industry](https://www.globalkeysolutions.net/guidances/guidance-document/expedited-programs-for-regenerative-medicine-therapies-for-serious-conditions-draft-guidance-for-industry/4c570099-1582-4019-8f81-d0260a2e984c) - [Tobacco Product User Fees: Responses to Frequently Asked Questions](https://www.globalkeysolutions.net/guidances/guidance-document/tobacco-product-user-fees-responses-to-frequently-asked-questions/45be5e37-e658-4740-a843-04fd276300bf)