For more information, contact:

Kyra Douglas
Senior Director, Global Regulatory Affairs

Project Passport helps companies communicate product safety and  compliance information more efficiently.Project Passport, developed by a work group in the Food, Drug, and Cosmetic Packaging Materials Committee (FDCPMC), is a collection of resources, available free as a service to the industry, that provide companies with a more effective way to communicate product safety and compliance information about packaging raw materials, components and articles moving through the food supply chain. It creates a recognizable and adaptable system whereby regulatory information can be transmitted to buyers, processors, brand owners and officials.

Available Documents

  • Guideline for Risk Communication

    This document includes an introduction to Project Passport as well as: 1) a form for declaration of compliance, 2) instructions that provide detailed context for the form and 3) interspersed 'quick guides' to provide added clarity on the instructions.

    Project Passport Guidelines

  • Declaration Form

    The declaration of compliance form can also be downloaded by itself as a fillable document (Microsoft Word .doc file). The form is generic by design such that it can be adapted to different products in various jurisdictions.

    Declaration Form

  • Supplemental Passport Guidance Documents

    In-depth supplemental guidance is now available on complex regulatory issues that pose special challenges for supply chain communication:

    Read the Good Manufacturing Practice (GMP) Guideline for the Plastics Food Packaging Supply Chain, which serves as a general reference tool for companies and facilities throughout the plastic packaging supply chain, from resin manufacturer through packaging converter. This document does not establish a GMP program that would be appropriate for any particular facility. Rather, this document serves as a guide for topics and areas that should be considered during development of a GMP program.

    Read GMP Guideline

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