REACH Testing Service

What We Help You Achieve with REACH Testing

• Risk mitigation. Identify Annex XVII and SVHC substances before shipment.

• Faster approvals. Get documented proof of compliance for customs and buyers.

• Supply-chain confidence. Screen 240+ SVHCs with every test.

• Cost optimization. Early screening avoids full re-tests and recalls.

EU REACH Compliance and Testing

EU REACH (EC 1907/2006) restricts the use of specific chemical substances in products sold in the European Union. Non-compliance can result in product bans, market withdrawal, and customs rejection. REACH testing is the standard method used to verify that your products are free from restricted substances and SVHCs - giving you documented proof of compliance before your shipment reaches EU buyers or customs authorities.

Restricted and Limited Substances

REACH compliance testing tests products for the presence of substances found on Annex XVII and Candidate List of SVHCs. If a chemical is present in any concentration and is listed on Annex XVII, it will fail testing and would be banned from the EU market. SVHCs require authorization to be used in any product and are generally allowed if the concentration is less than 0.1% of the total product weight. If the concentration is higher, the importer or manufacturer must disclose this to customers with correct labeling and to ECHA, and may be subject to restrictions.

QIMA’s REACH tests cover both Annex XVII restricted lists and the SVHC Candidate List, so you catch any regulated chemical at or above 0.1% of product weight.

Below are some of the chemicals REACH regulates:

Annex XVII Restricted Substances

• Phthalates

• AZO colorants in textiles

• Nickel release from metal products in direct contact with skin

• PCTs

• Benzene

• Asbestos fibres

• Arsenic compounds

• Mercury compounds

• Cadmium

• View full list

Candidate list of SVHCs (Substances of Very High Concern)

• Carcinogenic, Mutagenic or toxic to Reproduction (CMR)

• Persistent, Bioaccumulative and Toxic (PBT) or very Persistent and very Bioaccumulative (vPvB)

• Identified, on a case-by-case basis, from scientific evidence as causing probable serious effects to human health or the environment of an equivalent level of concern as those above (e.g. endocrine disruptors).

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Why Partner with QIMA For Your REACH Testing?

Trusted by 30,000+ businesses worldwide and ranked #1 for customer satisfaction in the TIC industry - here's what that means for your REACH compliance.

Our regulatory expertise in the EU is supported by:

• Global lab network. Accredited ISO/IEC 17025 labs in 40+ countries.

• Fast turnaround. 96.3% of reports delivered in 5-10 business days.

• Comprehensive scope. 240+ SVHCs tested and updated with each ECHA revision.

• Inspector sampling. Factory-collected specimens reflect real production.

• Online management. Book, track, and share test reports via myQIMA.

Join over 30,000 global brands and book your REACH testing today.

How REACH Works?

5-step REACH Testing Workflow:

1. Book & submit samples to your nearest QIMA lab.

2. QIMA runs full-scope or targeted SVHC/Annex XVII analysis.

3. Receive a detailed PASS/FAIL report with concentrations and photos.

4. Act on results with corrective-action support.

5. Integrate testing into your production cycle for ongoing compliance.

Step 1 - Book and send your samples Timeframe: Confirmation within 1 business day of booking

Book your REACH testing via myQIMA and ship 3–5 product samples to your nearest QIMA-accredited lab. We accept samples in over 40 countries across Asia, Europe, and the Americas. Your dedicated lab contact confirms receipt and opens your testing file within 1 business day - no paperwork queues, no ambiguity about what happens next.

What you need to provide:

• 3–5 representative product samples (sufficient quantity for full SVHC screening - your lab contact will confirm exact weights or volumes on booking)

• Product description and material composition where known

• Target market and applicable REACH scope (Annex XVII restricted substances, SVHC Candidate List, or both - if unsure, QIMA recommends based on your product category)

• Intended use and product category (e.g. textile, electrical & electronic equipment, toy, packaging, jewelry)

Step 2 - QIMA runs chemical analysis in an ISO/IEC 17025-accredited lab Timeframe: Testing begins within 1–2 business days of sample receipt

QIMA's ISO/IEC 17025-accredited laboratories analyze your samples against the full REACH Candidate List (240+ SVHCs) and the Annex XVII restrictions applicable to your product category. You can request full-scope screening or targeted analysis - our technical team advises the right scope based on your materials and market.

Step 3 - You receive a detailed PDF test report Timeframe: 5–10 business days from sample receipt (standard); rush options available

QIMA delivers a structured PDF test report stating a clear PASS or FAIL per substance and per parameter, along with detected concentration levels, the testing methodology applied, and specimen photographs. The report meets REACH-compliant documentation standards and is accepted by EU customs authorities, major retailers, and brand compliance teams for market access and buyer submission. If you require a Declaration of Compliance (DoC) or Safety Data Sheet support, our regulatory team can advise. Reports are delivered via your myQIMA dashboard — accessible at any time, tracked against your order.

All turnaround times run from confirmed sample receipt at the QIMA lab, not from booking date.

Step 4 - Act on the results Timeframe: Immediate - report delivered ready to use

If your product passes: Use the test report to demonstrate REACH compliance to buyers, customs, or retailers. The report is valid for EU market access documentation and can be archived on myQIMA for instant retrieval across your supply chain team.

If your product fails: QIMA's report identifies each non-conformance by substance, concentration, and material component - giving your supplier a specific corrective brief rather than a vague failure flag. Retesting after corrective action typically completes in 3–5 business days. QIMA's lab team can advise on reformulation or material substitution options where needed.

Step 5 - Integrate testing with your production cycle Timeframe: Set up once; runs with every order

QIMA's lab testing integrates directly with its inspection programs. When a QIMA inspector visits your factory for a Pre-Shipment Inspection or During Production Check, they can collect product samples directly from the production line on your behalf - eliminating supplier-selected sampling bias and giving you independently verified test specimens. Tested samples reflect what was actually produced, not what a supplier chose to send.

Ready to Prove REACH Compliance Before Your Products Reach the EU?

Test against 240+ SVHC substances in an ISO/IEC 17025-accredited lab. Results in 5–10 business days, accepted by retailers and customs authorities worldwide.

Recent REACH Updates

Candidate List Extension

On Nov 7, 2024, one new SVHC was added to the Candidate List (triphenyl phosphate), which now contains 242 substances.

REACH Testing FAQs

What is REACH testing?

Laboratory analysis to verify your product meets EU REACH limits on restricted substances and SVHCs.

1. How quickly will I receive my REACH test results?

Most standard REACH tests are completed within 5–10 business days from confirmed sample receipt at the lab. Rush turnaround is available for time-sensitive shipments - contact us at booking to confirm availability for your specific product and scope. QIMA delivers 96.3% of testing reports on or before the confirmed date.

2. What determines the price of REACH testing?

REACH testing is priced based on the number of samples, the substances in scope (targeted SVHC screening vs. full Annex XVII analysis), and the product category. A single-substance screen costs less than a comprehensive multi-material assessment. Get a quote for an exact figure based on your product - most clients receive pricing within 1 business day.

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3. How many samples do I need to send for REACH testing, and in what condition?

For most products, 3–5 representative finished product units or material samples are sufficient. The exact quantity depends on product complexity and the number of materials being tested - your QIMA lab contact confirms this at booking. Samples should be representative of the production batch you intend to sell into the EU market. Prototypes and pre-production samples are also accepted.

4. Do I need to know which REACH substances apply to my product before I book?

No. If you're unsure of your SVHC exposure or applicable Annex XVII restrictions, QIMA's technical team will recommend the right testing scope based on your product category, materials, and target market. You don't need prior regulatory expertise to get started - that's what QIMA's lab specialists are there for.

5. Which countries and product types does QIMA cover for REACH testing?

QIMA accepts samples in 40+ countries and operates ISO/IEC 17025-accredited labs across Asia, Europe, and the Americas. REACH testing is available for a wide range of consumer product categories including textiles, electrical and electronic equipment, toys, jewelry, furniture, packaging, and hardlines. If you are unsure whether your specific product falls within REACH scope, contact us — our team will advise.

6. My products are manufactured in Asia. Can QIMA still handle REACH testing?

Yes. QIMA's lab network in Asia means your samples can be tested close to the point of production, with no need to ship to Europe first. This reduces transit time and gets your compliance documentation in hand before your shipment departs - not after it arrives at EU customs.

7. Can I combine REACH testing with other compliance services?

Yes. Bundle with RoHS testing, AQL inspection or social compliance audits for complete market readiness.

8. What happens if my product fails REACH testing?

QIMA issues a detailed failure report that identifies each non-conformance by substance, detected concentration, and material component - giving your supplier a specific corrective brief, not a vague fail notice. You can choose to retest after corrective action, which typically completes in 3–5 business days. If you need guidance on reformulation or material substitution, QIMA's technical team can advise on next steps.

9. REACH adds new SVHCs to the Candidate List regularly. How do I know my testing covers the current list?

QIMA updates its testing scope in line with each ECHA Candidate List revision. When you book REACH testing with QIMA, your report is assessed against the current published list at the time of testing - currently covering 240+ SVHCs. If a new substance is added after your report is issued and you need to reassess, QIMA can run a targeted screen for the new entry without requiring a full retest.