REACH is a European Union regulation (1907/2006/EC) restricting the levels of specific chemical substances in all imported goods. Our REACH compliance testing helps you comply and schedule tests online.
REACH Compliance Requirements - Read about REACH requirements and who is responsible for registering chemicals with ECHA.
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.
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.
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
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).
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:
Accredited labs in 40+ countries ISO/IEC 17025-certified results, accepted by EU customs authorities and major retailers — wherever your products are made.
Results in 5–10 business days 96.3% of reports delivered on time. When your shipment window is tight, the number matters more than the claim.
240+ SVHCs tested, updated with every ECHA revision Your report reflects the live regulatory position — not a list that was current six months ago.
Inspector-collected sampling QIMA inspectors can collect samples directly from your production line — so your test specimen reflects what was actually made, not what your supplier chose to send.
Every order managed in myQIMA Book, track, receive reports, and share compliance documentation with buyers — all in one place, in real time.
Join over 30,000 global brands and book your REACH testing today.
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, jewellery)
QIMA's ISO/IEC 17025-accredited laboratories analyse 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.
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.
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Testing scope |
Standard turnaround |
Rush option |
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SVHC Candidate List screening (targeted) |
5–7 business days |
Available — confirm at booking |
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Full REACH scope (Annex XVII + SVHC) |
7–10 business days |
Available for select substance groups |
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Retest after corrective action |
3–5 business days |
— |
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Report delivery KPI |
96.3% on time |
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All turnaround times run from confirmed sample receipt at the QIMA lab, not from booking date.
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.
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.
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.
Candidate List Extension
On Nov 7, 2024, one new SVHC was added to the Candidate List (triphenyl phosphate), which now contains 242 substances.
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.
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.
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.
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.
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, jewellery, furniture, packaging, and hardlines. If you are unsure whether your specific product falls within REACH scope, contact us — our team will advise.
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.
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.
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.
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By contacting QIMA you agree to our privacy policy and terms and conditions.