As a pharmaceutical manufacturer, we perform packaging, labeling, and storage classification, and handle the import of pharmaceuticals. We also accommodate incoming testing conducted using external testing institutions.
Packaging
Labeling
Storage
Incoming Testing
Import
As a pharmaceutical manufacturer, our Pharmaceutical Logistics Center is located adjacent to the AI Co., Ltd. Kasugai Head Office. As a pharmaceutical manufacturer, we perform packaging, labeling, and storage. Our facility offers ample space, capable of storing more than 200 pallets. Please feel free to consult us regarding the storage of pharmaceutical APIs, excipients, and similar materials.
| Trailer Access Available | |
|---|---|
| Front Road | 8M |
| Logistics Center Loading Area | 9M×30M |
| Storage Categories | |
|---|---|
| Room Temp. 1°C–30°C | Pallet Storage |
| Adjustable within 1°C–30°C | Pallet & Bulk Storage |
| Poisonous Drug Storage 1°C–30°C | Bulk Storage |
Our company is made up of experienced, highly skilled staff who have worked in the pharmaceutical industry for many years. Our personnel are well versed in every phase of the pharmaceutical business, including research, manufacturing, quality control, and regulatory affairs, and we provide practical, hands-on consulting. We offer consistent support, from identifying issues from an on-site perspective to proposing improvements and providing operational assistance, delivering optimal solutions across a wide range of fields, including equipment-introduction support, manufacturing-process improvement, and quality-system development. As a partner who stays close to our customers' business growth, we deliver reliable results.
We provide GMP-related support services to overseas manufacturing sites and similar facilities. Through assistance with building manufacturing and quality-control systems, audit response, and improvement proposals, we support smooth business operations and quality enhancement based on Japan's GMP standards.
We support the export of high-quality Made-in-Japan pharmaceuticals. From partner matching with pharmaceutical companies and manufacturers through to obtaining the permits required for export, we provide comprehensive, one-stop support.
· Application agency services for foreign manufacturer accreditation
· Liaison services for handling inquiries during PMDA approval review
· MF registration and in-country manager (local agent) services
· Consulting services for overseas manufacturers on Japanese regulatory affairs guidance and development-related proposals and improvements
We seek out overseas API (Active Pharmaceutical Ingredient) manufacturers and supply high-quality, reasonably priced APIs to domestic manufacturers. In addition, our staff—skilled in both translation and interpretation—enable smooth communication, and through our local partner companies we gather information in real time.
For Japanese prescription and OTC pharmaceuticals that are highly regarded overseas, we provide seamless, end-to-end support spanning everything from matching with domestic and international pharmaceutical companies through to overseas sales and export assistance. By accurately grasping the needs of both parties, we facilitate smooth business development.
We provide one-stop services for the development, prototyping, and manufacturing of healthcare supplements tailored to your needs. We develop high-quality raw materials, create everything from the package design onward, and carry out product manufacturing at a health-food GMP-certified factory. During the manufacturing process, we can also perform toxicity testing, contents testing, and stability testing, and upon request we can arrange various tests at an impartial third-party institution. In addition, we can provide support for obtaining the documents issued by the Agricultural Administration Bureau that are required for export to China and South Korea (importation at the destination). (As of 2024: when required in connection with the nuclear power plant accident.)
We hold a consultation to understand your requests (what kind of supplement you would like to create, the desired contents, etc.).
Based on the consultation, we design the recipe for the contents. We also confirm material procurement and usability.
After the recipe design is complete, we create a prototype based on the design.
Using the completed prototype, we conduct accelerated stability testing.
* Harsh testing 6M (equivalent to 2 years); can be skipped if not required.
After the design is complete, experts verify whether the labeling complies with the relevant laws and regulations (Japanese law).
After prototyping is complete, we carry out the package design (including display labels).
Based on the consultation, we design the recipe for the contents. We also confirm material procurement and usability.
We deliver to the location you specify. Overseas shipping (CIF) is also available upon request.
We can also support the acquisition of the documents required by each country for overseas shipping (such as documents issued by the Agricultural Administration Bureau). Please feel free to consult us.
