Professionals of Pharmaceutical Development
Prepare documents

Prepare documents

Prepare documents for CTD or Investigator’s brochure
 
Translation

Translation

Translated by the highly skilled
 
Quality check

Quality check

Check document s carefully by the Experienced
 
Regulatory matters

Regulatory matters

Support of Regulatory matters
Developmental Supports

Developmental Supports

Developmental Supports
 
Seminar

Seminar

Planning and management of seminar
 
Contract out the studies

Contract out the studies

Research into laboratories that clients wish to contract out the studies(CROs overseas).
 
Safety evaluation research

Safety evaluation research

Support of conference and meeting

Characteristic of Three S Japan

Our staffs have abundant experiences in CMC, non-clinical studies and clinical trials,especially in the fields of pharmaceutical products. If clients make the most of outside specialized, professional team’s ability to develop drugs, for example, making response to the government agencies smoothly, advice on process in preparing documents, as a result that can present them with ways to cut down time and costs.

  • new information
  • new information