Quality & compliance
Built on processes, documentation, and responsible practices
At Systler, quality is approached as a system—not a slogan. Our products are developed, handled, and supplied through structured processes designed to support food safety, consistency, and regulatory alignment across markets.
We do not rely on exaggerated claims or cosmetic certifications. Instead, we focus on process discipline, traceability, and documentation that supports long-term compliance and partner confidence.
Regulatory alignment approach
Systler aligns its product development and handling practices with applicable food safety and regulatory requirements, including frameworks commonly referenced under FSSAI (India) and FDA (United States), where relevant to the market.
- Food-grade ingredient sourcing
- Defined handling and storage practices
- Batch-level traceability
- Labeling aligned with applicable regulations
Ingredient & supplier evaluation
Raw materials are sourced through evaluated suppliers based on quality parameters, consistency, and suitability for repeated consumption. Supplier documentation is reviewed as part of our procurement process.
- Supplier qualification checks
- Specification review
- Ongoing supplier performance monitoring
Processing, packing & hygiene
Products are processed and packed under controlled environments designed to support hygiene, minimize contamination risk, and maintain product integrity.
- Defined standard operating procedures
- Hygiene and sanitation controls
- Batch identification and records
Labeling & information transparency
Labels are designed to communicate essential product information clearly, without medical, therapeutic, or disease-related claims.
- Ingredient declaration
- Usage and storage guidance
- Regulatory-aligned disclosures
Documentation for partners
For distributors, retailers, and institutional partners, documentation is provided as applicable to support procurement and compliance processes.
- Product specifications
- Batch and traceability records
- Label reference information
Quality & Compliance FAQs
Common questions about our quality processes, documentation, and regulatory alignment.
Systler develops and supplies products using processes aligned with applicable FSSAI food safety and labeling requirements. Product compliance depends on the specific formulation, labeling, and intended market use.
Our quality systems and documentation are designed to align with commonly referenced FDA food safety frameworks where applicable. Final regulatory approval depends on importer responsibilities and product positioning.
Batch-level documentation such as specifications or analytical reports may be provided upon request, depending on the product and order type.
No. Systler products are positioned as everyday wellness or nutrition products and are not intended to diagnose, treat, cure, or prevent any disease.
Documentation supports procurement and internal review. Final audit acceptance depends on local authorities and buyer compliance policies.
Batch consistency is supported through defined processing procedures, supplier controls, and documentation at each stage.
Final regulatory approval rests with the brand owner, importer, or distributor in the destination market.
Need documentation or compliance clarification?
