Japan-sourced product information
for clinic evaluation.

AIC supports medical professionals and organizations seeking product information, initial implementation consultation, and supply discussions for Pure Stem-related products from Japan.

Structured information
before implementation.

Cross-border product evaluation requires more than a product name. We begin by clarifying intended use, destination, documentation needs, supply considerations and local requirements so that your organization can assess the next step appropriately.

Products for initial evaluation

Listed for general professional information. Specifications, availability and handling conditions are confirmed individually.

01

Stem Cell Conditioned Medium FD Rich

Information for adipose-, dental pulp- and umbilical cord-derived product lines.

02

Exosome Products

Initial product and supply consultation for clinics and medical organizations.

03

NMN

Product information for medical-professional and clinic-use evaluation.

04

Pure Stem Nasal Kit

Product-specific handling and documentation are reviewed case by case.

A clinic product-information evaluation setting
Information is organized around the product and your intended evaluation context.
Reviewing quality-related documentation
Specifications, quality-related information and handling conditions are reviewed together.

Documentation for a
more informed evaluation.

Drawing on the structure of manufacturer materials, we organize the practical information a clinic or medical organization needs before the next discussion. The available documentation is confirmed for your product, destination and intended use.

01

Product profile

Review the product name, source, volume, handling, storage and intended-use context.

02

Quality information

Clarify the available specification, composition or analysis, manufacturing and control documentation.

03

Implementation conditions

Discuss destination, availability, required procedures and relevant operational considerations.

Documentation availability, scope and disclosure are confirmed case by case and may vary by product, lot, intended use, destination and the policy of the manufacturer or relevant parties.

A practical review process

  1. 01

    Initial inquiry

    Tell us about your organization, specialty, intended use and destination.

  2. 02

    Information review

    We clarify the product information and documentation needed for your evaluation.

  3. 03

    Supply discussion

    Destination, availability and relevant requirements are reviewed case by case.

  4. 04

    Next-step guidance

    Where appropriate, we guide you through the next required discussion or process.

Japan-sourced information,
reviewed for your destination.

Japan-to-world medical information and supply consultation
We begin with the information and destination-specific questions your organization needs to review.

Professional information only

This page is for general information for medical professionals and organizations. Some listed products may include research materials for medical institutions and may not be intended for diagnosis, treatment or prevention. Product handling, import, distribution, advertising and use requirements vary by product, intended use and jurisdiction. Please complete your own legal, regulatory and professional review before any introduction or use. No efficacy, safety or clinical outcome is guaranteed.

Request information or a consultation

Please include your organization, country or region, product of interest and intended use.