Professionals of Pharmaceutical Development
Prepare documents

Preparation (MW)

Prepare documents for CTD or Investigator’s brochure

Translation (E-J, E-C)

Translated by skillful professional translators
Quality check

Quality check

Check document s carefully by the Experienced
Regulatory matters


Consulting about Development, applicaton and Quality Assurance
Regulatory matters

Regulatory matters

Support of Regulatory matters


Submission of J-DMF and Application of AFM

PV/PMS Service

We can support in Japan and overseas widely.

Agrochemical Service

We can adjust "Revaluation of Agrochemicals" from 2021 in Japan.

Characteristic of RPM

"Quality Of Life"+1

Our staffs have abundant experiences in CMC, non-clinical studies and clinical studies, especially in the fields of pharmaceutical products with most of available modalities. Actually, our specialized professional teams could make responses to regulatory agencies smoothly, and advice on process in CTA, IND, and NDA submission including preparing of required documents resulting in time and cost-effective drug development.

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Our Group Company

Domestic Group Company









Overseas Group Company