ISO 15848-1
ISO 15848-1:2015 is the internationally recognized standard titled “Industrial valves – Measurement, test and qualification procedures for fugitive emissions – Part 1: Classification system and qualification procedures for type testing of valves”. This standard specifies stringent testing methods to evaluate the fugitive emissions from industrial valves, especially those handling hazardous or volatile substances. ISO 15848-1 plays a vital role in environmental protection, plant safety, and compliance with emission regulations across the oil & gas, chemical, and pharmaceutical sectors.
By obtaining ISO 15848-1:2015 certification, organizations demonstrate their commitment to minimizing environmental impact, improving valve reliability, and complying with international emission norms.
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What is ISO 15848-1?
ISO 15848-1:2015 outlines a comprehensive classification and testing protocol for assessing the performance of industrial valves in terms of their fugitive emission control capabilities. It includes type testing procedures such as helium leak detection and endurance testing under defined temperature and pressure ranges. The standard categorizes valves based on tightness classes, endurance classes, and temperature classes, ensuring complete traceability and reliability of emission performance data.
This certification is crucial for manufacturers, suppliers, and end-users of valves who want to ensure that their equipment complies with environmental safety requirements.
Why is ISO 15848-1 important?
With the rising global focus on environmental sustainability and stringent emission norms, industries are under increased pressure to control and monitor fugitive emissions. ISO 15848-1:2015 ensures that the valves used in pipelines and process systems are qualified to contain hazardous emissions under real-world operating conditions.
Using valves certified under ISO 15848-1 builds trust with stakeholders, regulators, and clients, as it reflects the organization’s proactive approach to safety, compliance, and environmental care. This standard is also frequently referenced by industry-specific regulations and customer specifications, making it essential for global trade and supplier qualification.
What are the benefits of ISO 15848-1?
- Standardized Testing Protocol: Ensures that all valves meet uniform emission control benchmarks, improving industry-wide reliability and compatibility.
- Product Classification System: Helps users select valves based on emission, endurance, and temperature requirements specific to their operations.
- Enhanced Environmental Compliance: Supports adherence to regulatory frameworks such as EPA (Environmental Protection Agency) and EU Directives.
- Improved Valve Integrity: Reduces leakage, downtime, and potential health and safety hazards.
- Global Market Acceptance: Valves certified under this standard are widely accepted by multinational clients and industries worldwide.
What kind of businesses can benefit from ISO 15848-1?
Implementing ISO 15848-1:2015 delivers measurable advantages to organizations, including:
✅ Regulatory Compliance: Aligns the business with national and international emission control regulations.
✅ Risk Reduction: Minimizes operational and reputational risks associated with leaks of toxic or flammable substances.
✅ Operational Efficiency: Enhances equipment durability and reliability, leading to reduced maintenance and replacement costs.
✅ Market Competitiveness: Boosts credibility in tenders, approvals, and audits by demonstrating commitment to emission standards.
✅ Customer Confidence: Strengthens brand image and trust among clients who prioritize sustainable and safe supply chains.
✅ Sustainability Goals: Supports corporate environmental objectives and reduces carbon footprint.
Top Tips on making ISO 9001 effective for you.
#1
Top management commitment while practicing and accomplishing the standard is the key to success.
#2
Keeping staff informed about the ongoing practices, a well-communicated plan would increase the motivation and zeal of working in them.
#3
Making sure that the various departments of the organization work as a team for the benefit of the organization and customers as well.
#4
Review systems, policies, processes, and procedures for a smooth working of QMS.
#5
Speaking to customers & suppliers while getting feedback & working on improvements.
#6
Training staff carrying out the internal audits with the opportunity for improvement.
#7
Celebrate your achievement and use the QualityAsia Assurance Mark on your literature, promotional material, and website.
#8
Ensure continuous improvement by regularly reviewing and updating your quality management practices.
#9
Promote a culture of quality by encouraging innovation, accountability, and employee involvement at every level of the organization.
Why QualityAsia?
QualityAsia always vanguard in the auditing and governing of internationally acclaimed standards practices. At QualityAsia, we focus on driving the success of our clients through creating excellence with our trained professional auditors. The content of our service provision, comply with international certification rules defined by the accreditation bodies without burning a hole in your pocket. We will take you through the journey of audits with our best kept audit practices, viz.:
Initial Certification – Stage 1 (Preparatory Phase)
- Thorough documented information review.
- Exchange of information with staff through online or onsite presence.
- Identification of key performances, processes & objectives as per the standard requisites.
- Analysis of facilities, infrastructure, systems and processes in regard with the requested certification scope with a resource allocation review.
Initial Certification – Stage 2 (On-site Audit)
- Measurement, reporting & reviewing the performances against key performances objectives.
- Reviewing the suitability of the system meeting the legal, regulatory & contractual requirements.
- Operational control of processes, internal audits & management reviews while understanding the responsibilities for the policies.
- Conclusion based on prescriptive requirements, policy, performance objectives, staff skill, operations, procedures, internal audits, etc.
Surveillance & Certification Renewal
Drawing out the scrutiny on various aspects of the previously done audits on effectiveness while reviewing the various processes and control of the operations in the QMS and finally going for the recertification.
