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Medical equipment/cosmetics/pharmacies

Updated: July 2025, 10


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Example)Medical Device Approval StageCase

*The support process varies depending on the licenses and permits, so please check each page for details.

General flow of medical device approval stages

1. We will respond quickly so you can apply as early as possible.

By entrusting the application for new licenses for quasi-drugs to an administrative scrivener who specializes in such applications, you can enter the market as soon as possible.

2. Consultations are free. 

If you make a reservation in advance, we can also accommodate consultations outside of business hours, such as at night or on weekends and holidays.

3. We support building a compliance system for business operations.

Procedures (GVP, GQP) etc. can be created in a way that suits the actual situation.

4. We support the smooth start of business after obtaining permission.

Our staff will be responsible for collecting time and certificates from the pharmaceutical department, public health center, etc.

Pharmaceutical-related licenses and permits include "New business, change, renewal, closure" In addition to other duties, "Preparation of procedures, legal records and agreements""Compliance with pharmaceutical regulations""Implementation of in-house training""Conducting a self-checkThere are several daily tasks that need to be done, such as:

Even in the renewal investigation of pharmaceutical-related licenses and permits,Procedure manual revision record"Or"Checking business records according to procedures""Ingredient inspection records”, as well as “Implementation status of in-house training/evidence thereof""Status of internal audit implementation/improvement response" These are now becoming review points to ensure the creation of a more effective system.

In addition to the renewal surveys, the Pharmaceutical Affairs Division also conducts surveys on an irregular basis.


If you can outsource the management of pharmaceutical approvals, which are different from other approvals, to us,It is possible to complete procedures inexpensively and reliably while minimizing the burden on your company..

Our company is based in Tokyo, Nagoya, and Osaka.Available nationwideHas become.
For companies with multiple locations across Japan, we also provide support in managing pharmaceutical approvals and licenses.We utilize our know-how on the responses and procedural flows required for each region, jurisdiction, and person in charge to quickly support advance preparations, coordination with authorities, and applications. international success.

We can also help with these types of problems.

``The renewal date is approaching, but there is no way to prepare because I don't know what will be investigated.''

``I haven't reviewed the procedure manuals etc. since I got the permit...I'm not sure if it will be compliant with the renewal...''

``The person in charge of managing pharmaceutical affairs suddenly retired, and the procedures were not easy...''

“In the future, we would like to expand not only to cosmetics but also to quasi-drugs and medical devices, but is this possible with the current system?”

For those who need to obtain a Certificate of Origin when exporting.
Are you having trouble because the procedures are so complicated and you don't know where to start?

We provide support for obtaining a specific certificate of origin based on the EPA.
Why not leave the complicated procedures, from requesting origin determination to issuing certificates, to our experts?

[Expert explains]
Latest Topics on Pharmaceutical Affairs
(Medical devices, cosmetics, pharmacies)

Nationwide Support

In principle, we respond to inquiries on the same day or the next business day.

If you do not hear from us for more than 2 business days, the message may not have been sent.
We apologize for the inconvenience, but please contact us again using this form.

We also accept consultations over the phone.

    Free consultation available!
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    Free consultation available!
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