Can we begin without a complete product plan?
Yes. A reference product, target audience, sales channel, consumer need, or ingredient of interest can be the starting point, with the direction clarified together step by step.
WATERTRUST ZHUHAIZHUHAI · CHINAWATERTRUST ZHUHAI · COOPERATION GUIDE
Frequently Asked Questions
Answers to common questions before a project begins. Project-specific terms remain subject to discussion and confirmed documents.Can an existing product or reference sample be developed further?
An existing product, reference sample, and available information can guide development. A proven single product can also be extended into a series or supported by complementary products with distinct roles.
Can samples be refined after evaluation?
Yes. Consolidated feedback can identify what to retain and what to improve, with refinement based on formulation complexity, benefit direction, sensory feel, and stability. The exact arrangement is confirmed for each project.
Does the client provide packaging, or can Watertrust help?
Either approach is possible. Packaging may be supplied or customised by the client, or selected and ordered with Watertrust's support, with formula fit, filling method, label space, and user experience reviewed before confirmation.
Why do minimum quantities vary between products?
Product format, filling method, containers, sachet material, and other packaging supply conditions all affect minimum quantities. Practical material, scheduling, and split-delivery options can be discussed for each project.
How long do sampling and production take?
Timing depends on formulation complexity, revision rounds, efficacy testing, filing or registration documents, packaging procurement, and production scheduling. When production is time-sensitive, the final sample, bulk formula, container, packaging copy, and order terms should be confirmed early so filing, packaging, and production preparation can move forward in coordination.
What if we do not have our own trademark?
The product direction can still be discussed. Clients may prepare their own or legally authorised mark, or discuss an agreed Watertrust trademark authorisation option, subject to confirmed documents defining the mark, scope, and term.
What should a brand operator prepare before filing?
First confirm which party will act as the product registrant or filing entity, together with the brand and trademark route, sales market, and channels. Where the client company acts as the filing entity, it also needs an appropriate quality management system, adverse-reaction monitoring and evaluation capability, and clearly assigned quality-safety responsibilities. Watertrust can help organise product and manufacturing-side inputs for the contracted project.
What is the general filing path for ordinary cosmetics?
The usual path is to classify the product and confirm the filing entity; approve the final sample and formula, product standard, container, sales packaging, and label copy; complete applicable testing, safety assessment, and efficacy evaluation materials; establish and confirm the contracted-manufacturing relationship; review the dossier and submit it through the information service platform. Before market launch, the filed information, packaging label, and actual manufactured product should remain consistent. The exact sequence depends on the product and local regulatory requirements.
What information must appear on cosmetic packaging, and do trial packs also need it?
Cosmetic label copy must follow current national requirements and cannot be selected only for visual design. Applicable information generally includes the Chinese product name, relevant registrant or filing entity and contracted manufacturer information, product-standard number, full ingredient list, net content, shelf life, directions, and necessary safety warnings, subject to product classification and current rules. Trial packs or samples intended for sale, gifting, or public distribution should also be included in the applicable filing or registration and label-compliance arrangement. Samples used only for internal R&D, testing, or client approval are handled according to their actual purpose and project requirements.
What documents may a benefit-led product need?
This depends on product classification, sales market, and intended claims. Formula, label, testing, safety assessment, and efficacy evaluation materials may apply, subject to current requirements and project review.