NAL authorization is possible for every type of seed quality testing: germination, moisture, purity, the determination of usable plants in soil, health, varietal trueness and varietal purity et cetera. Also tests of e.g. leaf material for its health can be in the scope of the NAL laboratory. This was chosen to maximize the benefits of NAL authorization.
Naktuinbouw has expertise regarding all aspects of the authorization system: setting up the system, training the analysts and samplers, assessing test protocols and the organization of corresponding proficiency tests. Our experts monitor authorized laboratories via annual audits.
The NAL conditions are based on various guidelines and criteria. A complete overview of these conditions can be found in NAL conditions, v13.1.
NAL authorizes your laboratory for the following points:
Quality management system
The laboratory has an adequate and solid quality management system: this way, testing and sampling are safeguarded.
Representative sampling
Trained samplers take representative samples. The procedure has been approved by Naktuinbouw.
Approved test protocols
The laboratory performs the quality tests based on testing protocols that have been assessed and approved by Naktuinbouw.
Proficiency tests
The laboratory takes part in the (annual) program of proficiency tests.
Communication
Controlled communication of reliable quality information via standard NAL quality certificates.
Acceptance
NAL-authorized laboratories can include the test results when sending them to their clients. These results can also facilitate export. For example, Australia accepts purity tests and other seed determinations conducted by NAL laboratories. The NVWA often accepts test results from NAL laboratories as supporting documentation for phytosanitary certificates during export.
For more information, please consult our flyer.
Currently, the following (international) seed companies have a NAL authorization. Their scope (in broad terms) is mentioned in the authenticated register.
The Naktuinbouw board establishes our inspection fees each year. The fees are subsequently approved by the Minister of Agriculture, Nature and Food Quality. The costs are charged based on the cost-maker cost-bearer principle. The fees for authorization can be found here Fees (pricelist).
Would you like to apply for authorization of your laboratory, or would you like more information about our authorization system? Please contact Bureau Authorizations (see below).
Bureau Authorizations
+31 71 332 61 90 | Team Authorizations
Sample size and subsample sizes must be described and validated in your test protocol and/or validation report. See condition 22.8.6. This is reviewed by NAL.
You are always responsible to check requirements of third parties yourself. Third parties may request a test on a larger sample.
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Please click on the link Approved remarks on NAL quality certificates to view the complete list.
Click on the link Overview subcontractors to find an overview with subcontractors and their scope.
The sampling requirements as described in the NAL conditions version 12 will become into force from 1 October 2024. Tests performed after this date that are used for NAL quality certificates must meet these requirements. Small and commercial seed lots sampled and tested before 1 October 2024 are exempt from this requirement and seed health test results can be used for NAL quality certificates when tested according to in-house sample sizes.
For bacteria this is coming from requirements for GSPP (Good seed and plant practices, see GSPP : hygiene in seed production and plant raising to prevent infection with pathogens). Compared to bacteria, viruses and fungi have a different risk (a different infection rate and a different distribution) which leads to different number of seeds.
Small seed samples come from a (very) low number of plants. The ratio between the one plant infected with a pathogen and the other(s) is high, so the infection rate is high. The relevant number of seeds is extrapolated from ISPM no. 31, appendix 2, table 1 and can be calculated by the formulas in appendix 2.
Each test must reflect the whole sample, the sample can not be divided prior to starting the test protocol.