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GB/T 47292.1-2026Lithium-ion battery good manufacturing practice - Part 1: General requirements (English PDF)

锂离子电池生产质量管理 第1部分:总体要求

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Issued by

SAMR; SAC

Level / Type

National · Recommended

Issue date

March 31, 2026

Implementation date

April 1, 2027

Scope

GB/T 47292.1-2026 is the English-translated version of 锂离子电池生产质量管理 第1部分:总体要求.

GB/T 47292.1-2026 is Part 1 of GB/T 47292 and sets the general requirements for quality management in the production of lithium ion cells and lithium ion batteries.

It covers quality objectives and how they are formulated, measured and managed; quality planning through risk analysis, risk control and emergency management; resource requirements for organisation and personnel, environment, equipment and documents; quality control of key processes, from SPC to battery materials, manufacturing process and finished products and their release; error-proofing and traceability; the handling of nonconforming items; change management; and product quality review and analysis.

It applies to makers of power, energy storage and consumer lithium ion cells and batteries. It was issued on 31 March 2026 and applies from 1 April 2027.

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Document preview — GB/T 47292.1-2026

National Standard of the People's Republic of China

ICS
29.220.99
Classification
K 82

Issued by: State Administration for Market Regulation; Standardization Administration of the PRC

Contents

  • Foreword4
  • Introduction6
  • 1 Scope7
  • 2 Normative references7
  • 3 Terms and definitions7
  • 4 Abbreviated terms8
  • 5 General requirements9
  • 6 Quality objectives10
  • 6.1 Objective formulation10
  • 6.2 Objective evaluation indicators10
  • 6.3 Objective management11
  • 7 Quality planning11
  • 7.1 Risk analysis11
  • 7.2 Risk control11
  • 7.3 Emergency management12
  • 8 Resource requirements13
  • 8.1 Organization and personnel13
  • 8.2 Environmental management16
  • 8.3 Equipment maintenance and management17
  • 8.4 Document management20
  • 9 Key process quality control23
  • 9.1 SPC control23
  • 9.2 Quality monitoring of battery materials23
  • 9.3 Quality monitoring of manufacturing process23
  • 9.4 Quality monitoring of finished products25
  • 9.5 Product release requirements25
  • 10 Error-proofing and traceability management25
  • 11 Nonconforming item management26
  • 11.1 Identification26
  • 11.2 Transfer and isolation26

1 Scope

This document specifies the general requirements, quality objectives, quality planning, resource requirements, key process quality control, error-proofing and traceability management, nonconforming item management, change management, and product quality review and analysis in the lithium ion battery production process.

This document applies to the production process quality management of manufacturers of power, energy storage and consumer lithium ion cells and lithium ion batteries.

2 Normative references

The following referenced documents are indispensable for the application of this document. For dated references, only the version corresponding to that date is applicable to this document; for undated references, the latest version (including all amendments) is applicable to this document.

GB/T 19000, Quality management systems - Fundamentals and vocabulary

GB 50073-2013, Code for design of clean room

GB/T 47292.2-2026, Lithium ion battery good manufacturing practice - Part 2: Battery material control

GB/T 47292.3-2026, Lithium ion battery good manufacturing practice - Part 3: Cell process control and finished product testing

GB/T 47292.4-2026, Lithium ion battery good manufacturing practice - Part 4: Battery pack process control and finished product testing

JG/T 296-2010, Air shower

3 Terms and definitions

For the purposes of this document, the following terms and definitions, as well as those given in GB/T 19000, apply.

3.1 Lithium ion cell

A rechargeable device that achieves the conversion between chemical energy and electrical energy through the movement of lithium ions between the positive electrode and the negative electrode.

Note 1: It includes electrodes, separator, electrolyte, container and terminals, etc.

Note 2: Lithium ion cell is also generally referred to as "cell".

3.2 Lithium ion battery

An energy storage device consisting of one or more electrically connected cells or modules, capable of obtaining electrical energy from external sources and outputting electrical energy externally, and equipped with a battery management circuit.

Note 1: The battery management circuit usually has the functions of management or protection against overcharge, overcurrent, over discharge and/or overtemperature, so as to ensure the safety, performance and/or service life of the battery.

Note 2: The battery can be equipped with a protective enclosure and provided with terminals or other interconnection devices.

Note 3: The battery is also generally referred to as "battery pack" or "battery system".

3.3 Error-proofing

An engineering technology and management method that prevents errors, defects or accidents occurring in products or systems caused by human negligence, operation errors or unintentional actions from the source through design measures or process control.

4 Abbreviated terms

For the purposes of this document, the following abbreviated terms apply.

FMEA: Failure Mode and Effect Analysis

SPC: Statistical Process Control

5 General requirements

5.1 The enterprise shall establish and maintain a production quality management system for lithium ion cells or lithium ion batteries [hereinafter referred to as "lithium ion cells (batteries)"], and ensure that products or services conform to standards and meet customer requirements through quality planning, control and improvement.

5.2 The enterprise shall establish production quality management objectives for lithium ion cells (batteries), and specify the principles for objective formulation, evaluation indicators and management requirements for objectives.

5.3 The enterprise shall plan the production quality management of lithium ion cells (batteries), identify risk factors affecting quality and safety during the production process, and develop risk analysis, preventive measures and emergency management.

5.4 The enterprise shall establish resource management requirements for lithium ion cells (batteries), and specify the management of organizational responsibilities, personnel skills, production environment, production equipment, tooling and fixtures, as well as documentation.

5.5 The enterprise shall establish quality control specifications for key processes of lithium ion cells (batteries), including battery material quality monitoring, manufacturing process quality monitoring, finished product quality monitoring and product release requirements, and shall establish control plans and management requirements for key parameters affecting product safety, quality and reliability. The requirements cover the manufacturing and packaging stages of lithium ion cells. The schematic diagram of the life cycle of lithium ion cells (batteries) is shown in Figure 1.

5.6 The enterprise shall establish an error-proofing and traceability system for lithium ion cells (batteries), identify all materials (when one-to-one traceability of individual materials cannot be achieved, batch traceability may be applied), prevent confusion, misuse and release of nonconforming items, and achieve traceability throughout the product life cycle.

5.7 The enterprise shall standardize the management process for nonconforming items of lithium ion cells (batteries), including identification, isolation, disposition and records.

5.8 The enterprise shall establish a change management process for lithium ion cells (batteries), evaluate and manage changes affecting product quality, and specify the requirements for change application, evaluation, review, approval, implementation and records.

5.9 The enterprise shall establish a product quality review and analysis mechanism for lithium ion cells (batteries), including quality review, cause analysis, corrective and preventive actions, experience summary and horizontal deployment, so as to achieve effective problem resolution and continuous improvement.

6 Quality objectives

6.1 Objective formulation

The formulation of production quality objectives shall comply with the following requirements.

a) Specificity: the production quality objectives shall be specified in detail;

b) Measurability: clear data shall be available as the basis for measuring the achievement of objectives;

c) Achievability: the objectives shall be designed in accordance with the actual capability and acceptance of the responsible parties, and conditions for implementation shall be available;

d) Relevance: the objectives shall be consistent with the company's quality policy and long-term and short-term objectives;

e) Time-bound: the specific time for achieving the objectives shall be specified.

6.2 Objective evaluation indicators

The evaluation indicators for quality objectives include but are not limited to.

a) Failure rate at customer side and market side;

b) Process yield rate;

c) On-time delivery rate;

d) Material and component qualification rate.

6.3 Objective management

Objective management shall comply with the following requirements.

a) Managers shall authorize designated organizations or personnel to regularly monitor the implementation of objectives of each department, and provide feedback of the monitoring results to the objective implementers;

b) The enterprise shall establish response plans. When deviations occur in objectives (including process objectives), the objective implementers shall formulate improvement measures and plans for the deviations according to the response plans, track the implementation of the measures, and confirm their effectiveness;

c) The enterprise shall establish an escalation mechanism. When significant deviations occur between results and objectives, the situation shall be reported to the management level to ensure that management can timely understand the implementation of objectives and provide instructions;

d) The enterprise shall continuously improve objective management.

7 Quality planning

7.1 Risk analysis

The enterprise shall establish a quality risk analysis mechanism. The risk level shall be determined by evaluating the risk impact scope, severity of consequences, probability of occurrence and detectability. The risk analysis shall include the following.

a) Lessons learned extracted from historical scrapping, rework, product recalls, customer complaints, product returns and repairs;

b) Collecting and identifying relevant requirements for product safety, laws and regulations, product performance and services;

c) Establishing manufacturing process FMEA related to product safety and performance, and identifying and implementing control and inspection methods for safety- and performance-related characteristics during production and manufacturing processes.

7.2 Risk control

7.2.1 The enterprise shall determine and implement preventive measures.

a) Preventive measures include measures for preventing abnormal occurrence and measures for preventing the release of abnormal materials (including battery materials, semi-finished products and finished products);

b) Preventive measures shall be consistent with the risk level.

7.2.2 The enterprise shall establish a risk mitigation mechanism to reduce potential negative impacts. The mechanism includes but is not limited to the following aspects.

a) Determine potential nonconformities and their causes.

b) Develop and implement control measures for preventing nonconforming items, and establish an identification and interception mechanism covering the whole process of incoming materials, production and finished products, including.

1) Requirements for battery material control;

2) Requirements for production process control;

3) Requirements for semi-finished product process inspection;

4) Requirements for performance inspection before finished products leave the production line;

5) Requirements for monitoring and evaluation of finished product safety and reliability after stable production of finished products.

c) Form control measures as standard documents.

d) Review the effectiveness of control measures.

e) Establish an experience and lessons learned transformation mechanism, incorporate corrective and preventive actions into quality management system standard documents, and prevent recurrence of similar problems.

7.3 Emergency management

7.3.1 For manufacturing processes and infrastructure equipment that maintain production output and conformity with customer requirements, the enterprise shall identify and evaluate relevant internal and external risks, establish emergency management specifications, and develop response plans according to the following situations.

a) Risks and impacts on customers;

b) Ensuring continuity of supply under any of the following circumstances.

1) Failure of key equipment;

2) Interruption of externally provided products, processes and services;

3) Common natural disasters; […]

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This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 30 pages — is available in the English PDF.

Referenced standards

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