Comprehensive Services Across the Full Product Lifecycle

Every service we offer is built around your product’s unique regulatory journey — from first concept to global market presence.

Regulatory Strategy & Compliance

We develop and implement tailored regulatory strategies that align with your product type, target markets, and business timelines.

  • CE marking and EU MDR/IVDR compliance
  • FDA submission strategy and support
  • Regulatory gap assessments
  • Technical documentation preparation

Quality Management
Systems

We design, implement, and maintain robust QMS frameworks that satisfy global regulators and auditors at every stage.

  • ISO 13485, ISO 14971 & IEC 62304 aligned QMS
  • Internal, supplier & QMS health-check audits
  • QMS digitalization advisory
  • Certification audit readiness support

Risk Management & Clinical Evaluation

We build and maintain risk management files and clinical evaluation packages that meet current regulatory expectations worldwide.

  • Risk management files per ISO 14971
  • Clinical evaluation & PMS documentation
  • Benefit-risk analysis & reporting
  • Compliance with current regulatory guidance

SaMD Lifecycle & Technical Documentation

Specialized support for Software as a Medical Device throughout classification, development, and validation phases.

  • SaMD classification & development planning
  • Software architecture & requirements traceability
  • Cybersecurity & usability documentation
  • Verification & validation (V&V) support

Regulatory Submission & Communication

We prepare, compile, and manage your regulatory submissions while acting as your expert liaison with authorities and notified bodies.

  • 510(k), Technical File & Design Dossier preparation
  • Liaison with regulatory authorities
  • Notified body communication & audit support
  • Query response management

Post-Market & Vigilance Support

We establish and manage the post-market frameworks that keep your product compliant and your organization protected after launch.

  • PMS plan & report development
  • Vigilance & complaint-handling processes
  • CAPA management & continuous improvement
  • Field safety corrective action support
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