In the field of custom lubricating jelly, brand owners often pursue the perfect balance of quality, innovation, and cost-effectiveness. How to effectively control R&D investment and market launch time while ensuring high product quality and uniqueness is key to project success.
While many manufacturers claim to offer custom services, the true "king of cost-effectiveness" that can achieve "significant cost reduction and substantial cycle shortening" needs comprehensive strength in multiple aspects.
A mature formula library is core to reducing R&D costs and shortening cycles. Developing a new formula from scratch requires extensive experimentation and validation, with uncontrollable cycles. A factory with thousands of market-proven mature formulas (e.g., water-based, silicone-based, functional) can directly offer brand owners a rich selection. Brand owners can adjust and optimize based on these or select them directly, compressing new product R&D cycles by up to 60%-70%, and related R&D costs can be reduced by at least 40% or more.
Shared global compliance qualifications are key to saving certification costs and time. For products to be launched, especially in the medical device field or for export to international markets, relevant certifications (e.g., Class II medical device registration certificate, ISO 13485, FDA, CE) are essential. These certification applications are not only expensive (often costing hundreds of thousands or even millions) but also have long cycles of 1-2 years. If the cooperating factory already possesses these qualifications and can authorize their use, brand owners can achieve "zero-threshold" compliant market launch, directly saving this huge expense and long wait.
One-stop supporting services can further optimize cost structure. From product concept to final product, it involves multiple stages like packaging design, sampling, and regulatory consulting. If the factory can provide value-added services like free packaging design and free rapid sampling, it will undoubtedly save brand owners another considerable expense and improve project efficiency. It is estimated that this alone can save an average of about 200,000 RMB in R&D and design costs per project.
Pingchuang Medical, with its 2000+ mature formula think tank, complete global compliance certification system (FDA, CE, ISO 13485, etc.), full-process free one-stop services (free packaging design, sampling, free qualification authorization), and a daily output capacity of 600,000 units, truly achieves the goal of significantly reducing R&D costs and shortening market launch cycles for customers.
