Medical equipment/cosmetics/pharmacies

Manufacturing and sales of quasi-drugs for animals Manufacturing and sales approval

Updated: July 2026, 1


We provide application support and consulting to everyone, from those newly entering the veterinary quasi-drug industry to existing marketing distributors, manufacturers, and distributors.

Applications for veterinary quasi-drugs are highly specialized and can be said to be one of the fields in which there are few administrative scriveners who can handle them.

We have a track record of applications in all prefectures across the country, so please feel free to contact us.

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Specialist Team Support

The manufacture (import) and sale of quasi-drugs for animals requires many permits and licenses.
It is difficult for busy business owners to properly interpret and apply unfamiliar laws.
We will reduce your burden and contribute to increasing sales.

Quick and reliable responseResponse

Our motto is speed.
We handle your applications swiftly and reliably.

Consultation is free

Consultation before making a request is free of charge.

Whether a product falls under the category of quasi-drug for animals is determined by its efficacy.

This page introduces currently registered quasi-drugs for animals.

When selling the following items, the notation on the product container, packaging, and advertising media such as the WEB, etc.

Care must be taken to ensure that the standards and guidelines provided by the Ministry of Agriculture, Forestry and Fisheries are followed.

General flow of approval stages for quasi-drugs for animals

Consultation → Estimate The first consultation is free. Please contact us by phone or through the inquiry form. After that, we will ask you to visit us (or have a web interview) to confirm your current situation and provide you with advice. During the interview, we will listen in detail to your current situation and your requests, confirm the requirements necessary for the application, and provide you with an estimate at a fair price. Application If you are satisfied with the amount presented in the estimate and the service content, please place an order. Please consult with the person in charge about the timing of payment and success fee. Collection of materials and preparation of documents We will prepare the requirements necessary for the manufacturing and sales business and manufacturing business license application. We will hold meetings with government agencies as appropriate regarding details such as manufacturing equipment and personnel requirements. In parallel, we will prepare the application documents and attached documents. *Our specialized staff will prepare the complete set of application documents and hold meetings with government agencies on behalf of the client. Application agency Our administrative scrivener will apply on behalf of the client. The application fee will be collected before the application. If additional documents are requested, we will also handle it. Examination The examination will involve an on-site inspection. Our staff will also be present at the on-site inspection and take precautions in advance. If there are any instructions for corrections due to missing or revised documents, we will handle them. The review period is approximately 2-3 months after the documents are accepted, unless there are any issues. Notice of Permission If there are no issues after the review, you will receive a license. The license is valid for 5 years. Application procedures for each item An application for approval to manufacture and sell quasi-drugs for animals will be submitted. *Specialized staff will carry out the application procedures on behalf of the client. Application acceptance Once the application for approval to manufacture and sell quasi-drugs for animals is accepted, they can be manufactured and sold.

General flow of approval stages for quasi-drugs for animals

General flow of approval stages for quasi-drugs for animals

Nationwide support

    Free consultation available!
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    Free consultation available!
    Contact Us