Consultancy Services
Comprehensive advisory and consulting services designed to optimize regulatory compliance and market authorization.
Regulatory Strategy Development
Develop and implement customized regulatory roadmaps to accelerate product approvals and ensure global compliance across all phases.
Technical File Compilation and Gap Analysis
Detailed technical documentation and gap analysis ensuring compliance with international regulations and standards.
Clinical Evaluation Reports and Literature Reviews
Comprehensive clinical evaluation and literature review services following rigorous regulatory guidelines.
Quality Management System (QMS)
Design, implementation, and auditing of robust QMS aligned with ISO 13485 and FDA QSR requirements.
Global Regulatory Submissions
End-to-end support for global regulatory dossiers, FDA 510(k), PMA, CE Mark, and other key market authorisations.
Post-Market
Surveillance
Proactive vigilance and post-market clinical follow-up planning to maintain safety and ongoing regulatory compliance.
Your Trusted Partner in Compliance
We provide comprehensive, high-calibre regulatory solutions tailored to medical device, IVD, and pharmaceutical companies worldwide. Our team brings deep industry expertise to guide you through complex regulatory landscapes seamlessly, ensuring your products achieve rapid market entry and sustained compliance.
From early-stage product classification through rigorous clinical evaluation and global market authorizations, we empower life sciences leaders to innovate with confidence.
Read MoreComprehensive Regulatory Solutions
Tailored multi-disciplinary pathways across high-impact regulated healthcare and life science sectors.
Medical Devices
End-to-end lifecycle solutions
for Class I, IIa, IIb, and III medical technologies.
- Classification & Regulatory Strategy
- CE Mark (MDR 2017/745) Guidance
- FDA 510(k) & De Novo Submissions
- Risk Management (ISO 14971)
- Technical File Creation & Remediation
- Post-Market Clinical Follow-up
In Vitro Diagnostics (IVD)
Navigating complex diagnostic regulations, assay validation, and performance studies.
- IVDR (2017/746) Compliance Assessment
- Analytical & Clinical Performance
- Technical Documentation Dossiers
- Software & Usability (IEC 62304)
- Notified Body Interaction & Audits
- Global Market Authorizations
Cosmetics
Specialized compliance, product information files, and global safety assessments.
- Safety Assessments & PIF Preparation
- Regulatory Compliance Reviews
- Labeling & Claims Substantiation
- CPNP Notification & Registration
- GMP & Quality Assurance Protocols
- International Export Compliance
Meet Your Regulatory Expert
Imran Yousaf serves as the Principal Consultant of Veritas Quality Solutions. Drawing on deep expertise across a range of therapeutic specialties, Imran and his team support manufacturers with MDR transition, technical documentation, clinical evaluation, UK Responsible Person obligations, regulatory compliance, and related disciplines. His purpose is to simplify regulatory pathways so companies can focus on innovation.
What Our Clients Say
Trusted by leading healthcare, biotech, and medical device organizations worldwide.
"Veritas provided exceptional guidance through our MDR transition. Their methodical gap analysis and technical file restructuring saved our team months of costly delays."
Dr. Emily Watson
Chief Regulatory Officer
"Their proactive communication and deep technical acumen made our FDA 510(k) clearance seamless. They truly operate as an indispensable extension of our in-house team."
Marcus Sterling
VP of Product Development
"Navigating IVDR requirements felt insurmountable until Veritas stepped in. Their clinical evaluation report was thorough, rigorous, and commended by our Notified Body."
Sophia Ramirez
Quality Assurance Director