What is the purpose of 37 CFR 1.808?

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Source: FAQ (MPEP-Based) BlueIron Update: 2024-09-29 9 Rules 5 Related FAQs This page is an FAQ based on guidance from the Manual of Patent Examining Procedure. It is provided as guidance, with links to the ground truth sources. This is information only: it is not legal advice. 37 CFR 1.808 is a regulation that governs the furnishing of samples in patent applications related to biotechnology. This regulation is part of the Manual of Patent Examining Procedure (MPEP) Chapter 2400 on Biotechnology , specifically within Section 2410 – Furnishing of Samples . The purpose of this regulation is to ensure that biological materials referenced in patent applications are available to the public, which is crucial for enabling others to reproduce and verify the claimed invention. This aligns with the patent system’s goal of promoting the progress of science by requiring full disclosure of inventions. Related Rules from the Manual of Patent Examining Procedure 9 rules Collapse Deposit Must Be Available During Pendency and Post-Grant MPEP 2410 Required Deposit Restrictions Must Be Removed Upon Patent Grant MPEP 2410 Requirement for Sample Request During Patent Term MPEP 2410 Required Notification Required for Sample Filing During Patent Term MPEP 2410 Certification of Deposit Availability Upon Patent Grant MPEP 2410 Access to Patent Applications Except PTAB Proceedings MPEP 1002.02(b) Board Proceeding Record Available to Public MPEP 103 Access to Firm's Patent Applications for Registered Members with Signatory Power MPEP 104 Required Procedure for Making PTO Board Decisions Public MPEP 103 Other Related FAQs 5 FAQs Collapse How does 37 CFR 1.808 relate to biotechnology patents? What are the requirements for furnishing samples under the Budapest Treaty? What are the requirements for furnishing samples under 37 CFR 1.808? What restrictions apply to the furnishing of samples of biological materials? What is the significance of the term of deposit for biological materials?