Workflow of OEM
We will introduce the workflow from receiving your inquiry
to making your cosmetics and quasi drugs commercially.
New product meeting
We will hear from you about your wish and idea in detail.
Product (use), Product concept, ingredients you like to use, ingredients which use is prohibited, lot you plan, packaging you imagine (container, box, shrink-wrap, etc.), sales channel, sales price, unit price you plan (budget estimate)
Submitting a prototype
Our development department chemists and staff turn your ideas into a prototype that you plan to have. The prototype is free.
(If more than twenty prototypes are needed or expensive materials are used due to your request, let us ask you to bear the cost.)
Determining the formulation
Determining the prototype that we offered, we will proceed to prepare for commercialization.
Naming the product.
Preparing containers, fancy boxes, etc. (We are pleased to introduce you a buyer, so please consult us.)
Antibacterial effect validation , stability validation, Leak and Transformation test with the container.
Preparing for an estimate and a contract
We will make an estimate for the products based on the specification and quantity you like.
We have a standard form of contract of the products. After you look it over, you will make a contract with us.
Placing an order
After determining product specification, we will make notification according to Pharmaceuticals and Medical Devices Law.
We will place an order for the materials.
We will manufacture the products one by one carefully in the good and clean working conditions in our own plant.
We will conduct bacteria inspection and pre-shipping inspection and ship only the products that have passed those inspections.
The contents of the above may vary depending on the products.
We would appreciate it if you would consider it a rough workflow. We will explain the detail.
We will do our best.