Actria Services
Medical Device Regulatory Affairs Consulting
Preparing for launch in 2027

Medical device regulatory affairs consulting for companies building safe, compliant, and clinically meaningful products.

Actria Services is preparing to support medical device and healthcare technology businesses with regulatory strategy, submission planning, and practical execution for the Japanese market.

Services

Focused support for medical device regulatory affairs.

We support regulatory pathway planning, PMDA consultation readiness, and practical submission work.

01

Regulatory Strategy

Support for regulatory pathways, product positioning, documentation strategy, and review risk assessment.

02

Submission Planning

Practical support for technical documentation, evidence planning, and submission package readiness.

03

Japan Market Readiness

Consulting designed for companies preparing medical device products for the Japanese regulatory environment.

Leadership

Founding team

Founding members preparing Actria Services for its planned 2027 launch.

Chief Executive Officer

Kazuhiro Shiraki

Chief Operating Officer

Kenta Sato

Note: Actria Services, Inc. / 株式会社アクトリアサービシーズ is preparing for a planned 2027 launch. Details may be updated as business preparation progresses.