Management System Documents
- Organization chart
- Procedure documents
- Process documents
- Internal audit records
- Management review records
- Training records
- Corrective action records

Helping manufacturers, exporters and brands navigate product certification, system certification, ESG compliance and global market access requirements.
System Certification
Our consulting team supports companies in building management systems, preparing audit documentation, improving internal processes and getting ready for third-party certification audits.
Factories, trading companies, service providers and supply chain organizations
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Factories, laboratories, industrial sites and suppliers with environmental compliance obligations
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Factories, industrial sites, construction-related suppliers and operational teams
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Medical device manufacturers, component suppliers and healthcare product supply chains
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Food, cosmetics, health product and controlled production supply chain businesses
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Testing laboratories, calibration laboratories and internal company labs
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Preparation
Typical preparation materials include organization structure, procedures, process records, internal audit evidence and corrective action records.
FAQ
The required certification depends on product type, target market, intended use, electrical or chemical risks, buyer requirements and sales channel. Belling Global reviews the product information and maps a practical route before testing or documentation work starts.
Belling Global provides certification support, testing coordination, documentation review and market access consulting. Where an official certificate must be issued by an accredited certification body or notified body, we help clients prepare the correct route and documents.
CE is an EU conformity framework, FCC focuses mainly on U.S. radiofrequency and EMC requirements, RoHS restricts hazardous substances in electrical and electronic equipment, and REACH covers chemical registration and substance restrictions in the EU supply chain.
Yes. We can help identify applicable standards, arrange testing where needed, review labels and manuals, prepare technical file materials and organize compliance evidence for buyer or market access review.
Timeline depends on product complexity, selected standards, sample readiness, laboratory schedule, document completeness and whether third-party audit or certification body review is required.
Typical documents include product specifications, user manuals, technical drawings, circuit diagrams, BOM, label artwork, existing reports, target market information and, for system certification, procedure records and internal audit evidence.
Yes. Belling Global can compare requirements across the EU, U.S., UK, Canada, Australia, China, Japan, Korea, Southeast Asia and Middle East markets to build a phased market access plan.
Yes. We support ISO 9001, ISO 14001, ISO 45001, ISO 13485, ISO 22000, HACCP, GMP, IATF 16949 and ISO/IEC 17025 laboratory accreditation preparation where applicable.
Tell us your product, target market or certification needs. Belling Global will help you build a clear compliance pathway.
Tell us your product, target market and compliance needs. Our TIC specialists will respond as soon as possible.