Frequently Asked Questions

The general process includes requirement consultation, product specification confirmation, quotation, formulation design, sample testing and adjustment, packaging material confirmation, regulatory and labeling review, mass production scheduling, quality inspection, and delivery. The actual process may be adjusted depending on product complexity and customer requirements.

The timeline varies depending on formulation complexity, the number of sample adjustment rounds, ingredient and packaging material lead times, testing requirements, and production scheduling. If requirements are clearly defined and ingredient supply is stable, the development timeline may be shortened. We recommend confirming the product launch plan with your project contact in advance.

The minimum order quantity varies depending on the product dosage form, capacity, packaging format, ingredient conditions, and process requirements. After you provide the expected specifications, sales channels, and required quantity, our sales team will help evaluate a suitable production plan and quotation.

HANTECH uses high-specification retort pouches and a high-temperature, high-pressure commercial sterilization process. The four-layer laminated packaging material provides excellent barriers against air, oxygen, and light, helping prevent oxidation. This allows products to be stored safely at room temperature for extended periods without added preservatives.

HANTECH uses food-grade, heat-resistant laminated packaging materials that comply with national standards and provide excellent barrier properties. Packaging materials are regularly tested by third-party laboratories such as SGS to verify the absence of plasticizer and heavy metal residues. Even after high-temperature sterilization, the packaging maintains stringent safety standards.

Before shipment, all products must pass strict physicochemical testing by HANTECH’s in-house quality assurance laboratory. HANTECH also provides testing support by sending finished products to third-party laboratories such as SGS for testing of heavy metals, plasticizers, or key ingredients, providing strong quality assurance for the market.

The R&D team has established strict sensory evaluation and physicochemical standards. Scientific data, such as pH and Brix values, are used to support sensory testing. Combined with precise formulation ratios, this approach helps manage natural variations in ingredients caused by season or origin and ensures consistent flavor and taste across production batches.

From incoming ingredient inspection and process control to packaging inspection and finished product release, HANTECH follows established food safety and quality management systems. Batch management, inspection records, and traceability mechanisms are used to ensure that every production batch meets the quality specifications agreed upon by both parties.

Based on the product formulation and sales market, HANTECH can provide preliminary regulatory guidance on ingredient use, food additives, nutrition labeling, and packaging copy. Product names, advertising claims, and final label content must still be confirmed in accordance with the regulations of the actual market in which the product will be sold.

HANTECH treats customer business confidentiality as a top priority. A strict confidentiality agreement is signed at the beginning of the partnership, and comprehensive intellectual property protection mechanisms are applied from ingredient procurement and sample development through mass production to ensure that proprietary formulations remain confidential.

If you choose functional ingredients that require patent authorization, HANTECH can help confirm whether the actual dosage meets the original manufacturer’s standards and assist the brand with compliant applications for trademarks and patent licensing, helping enhance the credibility of the finished product.