Helping regulated products enter the USA, UK & EU with confidence and compliance. Your brand beyond borders.

I am an International Regulatory Compliance professional specialising in helping companies place regulated products on the United States, United Kingdom and European Union markets in a compliant, structured and commercially viable way.

My work focuses on regulatory strategy, market entry and risk mitigation. I support manufacturers, exporters and importers with services such as facility registrations, U.S. Agent or Responsible Person services, cosmetic listings, Prior Notice submissions, regulatory label reviews, documentation assessment and compliance consulting.

I work with regulated products including food and beverages, dietary supplements, cosmetics, OTC products, textiles, chemicals and other consumer goods subject to regulatory oversight. My approach is thorough and detail-oriented. I do not provide superficial reviews or checklist-based services. Each project is handled with the same level of care and responsibility required in regulatory environments where errors can lead to misbranding, detention, delays or enforcement actions.

I am used to working with international clients and understand the practical challenges of exporting and entering new markets. My role is to translate complex regulatory requirements into clear, actionable guidance, always balancing compliance obligations with business realities.

Clients work with me when accuracy, accountability and regulatory risk reduction are critical. I value transparency, clear communication and realistic expectations, and I take full ownership of the services I deliver within the agreed scope.

Work Terms

Payment Terms:
All payments are non-refundable once the service has started. Regulatory services involve time, expertise and submission of information to regulatory systems, and therefore cannot be reversed.

Regulatory Disclaimer:
Any registration, report, assessment, review or consulting service provided does not constitute a guarantee of approval, acceptance or clearance by regulatory authorities. Final decisions are always at the discretion of the applicable regulatory body (FDA, UK authorities, EU authorities, or others).

Client Responsibilities:
The quality, accuracy and timeline of the service depend on the client providing complete, accurate and truthful information in a timely manner. Delays, omissions or incorrect information supplied by the client may affect project timelines, outcomes or compliance status.

Scope of Services:
All services are performed strictly within the agreed scope described in the service listing or proposal. Additional products, countries, SKUs, variations or changes in scope may require a new agreement or additional fees.

Communication:
Clear and timely communication is essential for regulatory work. I am committed to professional, transparent communication and expect the same level of cooperation from the client to ensure smooth project execution.