Comprehensive Regulatory Solutions
End-to-end consulting for medical devices, pharmaceuticals, and healthcare staffing
Our Service Categories
Medical Device & Diagnostics
Navigate FDA, CE Mark, and CDSCO pathways with expert guidance.
- FDA 510(k) & PMA Submissions
- CE Mark (MDR/IVDR)
- CDSCO Approval
- ISO 13485 QMS
- Clinical Evaluations
Pharmaceuticals
Strategic regulatory affairs for drug development and approval.
- Drug Registration
- Clinical Trial Authorization
- Pharmacovigilance
- GMP Compliance
- Regulatory Intelligence
Staffing & Recruiting
Connect with top regulatory talent across healthcare sectors.
- Regulatory Affairs Specialists
- QA Professionals
- Clinical Research Associates
- Medical Writers
- Compliance Officers