Rin Authorization Gateway
Virginia Department of Health Professions
The Virginia Department of Health Professions licenses and regulates over 500,000 healthcare practitioners across 62 professions to ensure safe and competent patient care. They enforce standards and provide information to practitioners and the public.
The Virginia Department of Health Professions (DHP) is an Executive Branch agency dedicated to ensuring safe and competent patient care. They achieve this by licensing health professionals, enforcing practice standards, and disseminating information to both healthcare practitioners and the general public. DHP comprises Virginia's 13 health regulatory boards, the Prescription Monitoring Program, and the Health Practitioners' Monitoring Program. Collectively, they license and regulate over 500,000 healthcare practitioners across 62 distinct professions. The department also receives complaints regarding Virginia healthcare practitioners who may have violated regulations or laws. Key services include license lookup, complaint filing, and access to consumer information and case decisions.
About
**Who they are**
Rin Authorization Gateway is a specialized entity focused on regulatory compliance within Japan. They are dedicated to ensuring that companies meet the stringent requirements for marketing authorization and designated marketing authorization within the Japanese market.
**Expertise & scope**
* Expertise in navigating the Japanese regulatory landscape for pharmaceuticals and medical devices.
* Support for companies seeking to establish or maintain Marketing Authorization Holder (MAH) and Designated Marketing Authorization Holder (DMAH) status in Japan.
* Services include regulatory liaison and ensuring compliance with the Pharmaceuticals and Medical Devices Agency (PMDA).
* Proficiency in both Japanese and English to facilitate clear communication and documentation.
**Reputation / proof points**
* Coverage specifically for Japan (JP).
Rin Authorization Gateway is a specialized entity focused on regulatory compliance within Japan. They are dedicated to ensuring that companies meet the stringent requirements for marketing authorization and designated marketing authorization within the Japanese market.
**Expertise & scope**
* Expertise in navigating the Japanese regulatory landscape for pharmaceuticals and medical devices.
* Support for companies seeking to establish or maintain Marketing Authorization Holder (MAH) and Designated Marketing Authorization Holder (DMAH) status in Japan.
* Services include regulatory liaison and ensuring compliance with the Pharmaceuticals and Medical Devices Agency (PMDA).
* Proficiency in both Japanese and English to facilitate clear communication and documentation.
**Reputation / proof points**
* Coverage specifically for Japan (JP).
Additional information
Engaging Rin Authorization Gateway requires understanding their focus on the Japanese market. Their services are tailored to the specific regulatory framework governed by the PMDA. Buyers should be prepared to provide detailed product information and documentation to facilitate the authorization process. The dual language capability in Japanese and English is a significant advantage for international clients navigating local requirements. Clarify the exact scope of support for MAH and DMAH applications during initial discussions to ensure alignment with your product's lifecycle needs.
Key Highlights
Certifications & Trust Signals
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The Virginia Department of Health Professions licenses and regulates over 500,000 healthcare practitioners across 62 professions to ensure safe and competent patient care.
Source
“The Virginia Department of Health Professions licenses and regulates over 500,000 healthcare practitioners across 62 professions to ensure safe and competent patient care. They enforce standards and provide information to practitioners and the public.”
Buyer Snapshot
Best for
- Companies seeking MAH/DMAH services in Japan
- International firms needing to comply with Japanese regulations
How engagement typically works
- Regulatory liaison
- Documentation support
Typical deliverables
- MAH/DMAH application support
- Regulatory compliance guidance for Japan
Good to know
- Best when focused on the Japanese market (JP)
HQ:
Sendai, US
Languages:
Japanese, English
Timezones:
Asia/Tokyo
Status:
listed
Services & Capabilities
Japan MAH / DMAH Services
Jurisdictions:
JP
Countries:
JP
Industries:
Medical devices, IVD, Life sciences
Portfolio:
1-5
Onboarding time:
14–60 days
Pricing model:
Custom pricing
Starting from:
USD 6,000
Included services:
MAH/DMAH appointment support, PMDA liaison and communications routing, Local license/establishment maintenance support, Translation enablement (scope-dependent), GMP/QMS coordination support (scope-dependent)
Offers MAH:
No
Offers DMAH:
No
PMDA Support:
No
Local License Capability:
No
Translation Support:
No
GMP Qmssupport:
No
Regulatory Liaison PMDA:
No
Additional jp_mah_dmah Details
Included Services Detailed
MAH/DMAH onboarding and mandate setup (seed scope), PMDA liaison and communications routing (seed scope), Local license/establishment maintenance tasks (seed scope), Translation enablement for core regulatory documents (seed scope), GMP/QMS coordination support for audit readiness (seed scope)
Excluded Services
Manufacturing or supply chain execution, Acting as commercial distributor by default, Legal representation in disputes or litigation
Onboarding Steps
Insufficient public detail to generate onboarding steps without boilerplate.
Service Notes
This seed profile is unverified and intended for initial directory population.
Offers MAH
Yes
Offers DMAH
Yes
PMDA Support
Yes
Regulatory Liaison PMDA
Yes
Translation Support
Yes
