According to the current legislation in Türkiye, the analysis of non-medical veterinary products is considered mandatory in various situations to enhance animal health, food safety, and market surveillance.
Situations Requiring Mandatory Analysis of Non-Medical Veterinary Health Products
- Before Placing on the Market
To place non-medical veterinary health products on the Turkish market, notification must be submitted to the Ministry of Agriculture, Forestry, and Climate Change. During the notification process, the submitted dossier may require not only the product’s formula and ingredient quantities but also microbiological test reports, challenge test reports, and test data supporting the product’s claims. These reports are obtained through the analysis of the product.
- Market Surveillance and Controls
In routine inspections conducted by the Ministry or in response to complaints or alerts regarding a product, sample analysis may be required. If non-compliance or a defect is detected, it may result in stricter inspections and a requirement for ongoing analysis by the company.
- Production Process and Quality Control
A production license must be obtained from the Ministry for the manufacturing of such products in Türkiye. Companies with production authorization are expected to perform regular analyses. Additionally, analyses are necessary to ensure quality control, verifying that the product maintains its stability and effectiveness throughout the declared shelf life.
- Ensuring Animal-Derived Food Safety
For non-medical veterinary health products used on food-producing animals, it is essential to regularly analyse whether residues remain in animal-derived products such as meat, milk, or eggs. The Turkish Food Codex and related legislation define maximum residue limits and require that products comply with these thresholds.
What Are the Benefits of These Analyses?
In the cases mentioned above, conducting analyses is mandatory in order to operate in the Turkish market. This requirement aims to ensure animal health and welfare, improve and protect food safety and public health, enhance legal compliance and market surveillance, and minimize issues that could harm the brand.
Chemleg is ready to assist you in the analysis process of your non-medicinal veterinary health products.
Chemleg is ready to assist you throughout the analysis process of your non-medical veterinary health products.
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Frequently Asked Questions
Which regulations apply to the analysis of non-medical veterinary health products?
Non-medical veterinary products fall under the Regulation on Non-Medical Veterinary Health Products and are also related to the SEA and KKDIK regulations.
Is product analysis mandatory?
Yes. It is mandatory to analyse non-medical veterinary health products to ensure their safety and compliance with legal requirements.
What if my product fails the analysis?
Products that do not meet the required criteria cannot be placed on the Turkish market. In such cases, Chemleg will provide the necessary corrective suggestions to help make your product compliant.
Is an analysis report required for export?
Yes. Many countries require valid analysis reports and compliance certificates for imported products. Chemleg also offers consultancy services for export processes.
Who conducts and supervises the analyses?
In Türkiye, such analyses are generally carried out by official laboratories affiliated with the Ministry of Agriculture, Forestry, and Climate Change or by private laboratories authorized by the Ministry. Inspections are conducted by the Ministry’s relevant departments.