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Quality & compliance for botanical ingredient exports

Systler coordinates supplier qualification, product specifications, testing, documentation and shipment requirements around the ingredient you are buying, your application and your destination market.

Quality and compliance coordination for botanical ingredient exports
Our approach

Quality built around the agreed specification

Botanical ingredients are not adequately qualified by a single certificate or a generic test list. The required specification can change with the product, grade, application, buyer, destination market and commercial order.

Systler therefore approaches quality as a coordinated process. We review the required product specification, available supplier or manufacturer evidence, testing requirements, documentation and shipment needs before confirming the appropriate commercial supply.

Quality framework

How we coordinate quality

The exact controls and evidence depend on the selected product and supply route, but our review follows a consistent commercial and technical framework.

Supplier qualification

We review the supplier or manufacturer against the product requirement, available facility information, certifications, technical capability, documentation and commercial suitability.

Specification review

Product form, grade, purity, mesh or particle size, active parameters, physical characteristics and other relevant requirements are reviewed against the buyer's intended specification.

Evidence review

Available specifications, certificates, declarations, laboratory reports and other supporting evidence are reviewed according to the requirement before they are relied upon for the transaction.

Testing coordination

Independent laboratory testing can be coordinated for the parameters required by the agreed specification, buyer or destination market.

Documentation coordination

Product, quality and export documentation is assembled around the selected ingredient, supporting evidence, agreed testing scope and shipment.

Shipment verification

Before commercial dispatch, the agreed product, packing, required documentation and applicable shipment requirements are coordinated against the order.

Testing

Testing according to product and buyer requirements

There is no single universal test panel for every botanical ingredient. Testing is selected according to the product, agreed specification, application, destination market and buyer requirements.

Testing area Examples of parameters When applicable
Identity & physical Botanical identity, appearance, colour, odour, moisture, ash, mesh or particle size According to the product specification and agreed test method
Microbiological Total plate count, yeast & mould, coliforms, E. coli, Salmonella and other required organisms According to application, buyer limits and destination requirements
Heavy metals Lead, arsenic, cadmium, mercury and other required elements Limits and methods matched to the agreed requirement
Pesticide residues Multi-residue screening and specified pesticide parameters Where required by the buyer, application or destination market
ETO / 2-CE Ethylene oxide and 2-Chloroethanol Where required for the selected product or market
Product-specific parameters Examples include psyllium purity and swell volume, withanolides, curcumin, thymoquinone, coumarin and other relevant parameters According to the selected botanical and commercial specification
Additional testing Aflatoxins, allergens, contaminants and other requested parameters Coordinated where applicable to the transaction
Evidence & documentation

Documentation matched to the transaction

The documentation package is built around the selected ingredient, supporting supplier or manufacturer evidence, agreed specification, buyer requirements, destination market and shipment.

Company & export documentation

IEC registration FSSAI Central Licence APEDA RCMC where relevant Other applicable company documentation

Product & quality documentation

Technical specification sheet COA / laboratory reports according to requirement Allergen and product declarations where applicable Supporting supplier or manufacturer evidence where applicable

Shipment documentation

Commercial invoice and packing list Certificate of origin where applicable Phytosanitary documentation where required Transport and other applicable export documents
Destination markets

Requirements vary by market and application

We use the destination country as an input to the sourcing and documentation process rather than treating one compliance package as suitable for every market.

United States

Tell us the intended use and required US documentation or testing. Where facility registration, specific testing, declarations or other supporting evidence is required, it is reviewed against the selected supply.

European Union

EU-bound requirements can involve product-specific contaminant, pesticide, microbiological and documentation criteria. The required scope is reviewed against the ingredient and buyer specification.

Other international markets

For GCC, UK, Canada, Asia-Pacific and other destinations, specify the importing country and any required certifications, tests or declarations so the appropriate supply and documentation can be reviewed.

Buyer questions

Quality & compliance FAQs

COA and laboratory documentation are coordinated according to the agreed product specification and commercial requirement. The exact parameters and testing scope depend on the ingredient, selected supply, buyer requirements and destination market.

Yes. Independent laboratory testing can be coordinated for required parameters such as microbiology, heavy metals, pesticides, ETO and 2-Chloroethanol, active compounds and other product-specific requirements.

Yes. We review documentation and testing requirements against the selected ingredient, buyer specification and destination market, and coordinate the applicable supplier, product, laboratory and export documentation.

Available specifications, representative documentation and relevant supporting evidence can be reviewed during qualification where available. Commercial-lot documentation is coordinated according to the agreed order and testing requirements.

The importer, brand owner or finished-product manufacturer remains responsible for confirming country-specific import, product and finished-product compliance. Systler coordinates documentation and testing to support the agreed ingredient transaction.

Discuss your requirement

Tell us the specification, testing and documentation you need

Share the ingredient, quantity, destination and required quality parameters. We will review the appropriate sourcing, testing and documentation route for your requirement.