Regulatory Affairs

Obtain, Authenticate and Legalize Documents Anywhere.

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Regulatory Affairs Documents

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Regulatory support for regulated industries including the Pharmaceutical & Healthcare sector, specializing in Worldwide Market Authorization support, including certificate of pharmaceutical product.

Regulatory Documentation Support

We provide a comprehensive list of services for the pharmaceutical and healthcare sectors, including global legalization services and submissions and filing in both the United Stats & overseas markets.

Our service for Regulatory documents was initiated in the early ‘90s as a result of the increasing level of services requested by our existing client base. In addition to providing a comprehensive external legalization service, we also provide both external and in-house support for our clients’ global submission of documents to the relevant Health Authorities.


We process 1000’s of documents for legalization on a weekly basis, and a significant proportion of this volume are CPP, GMP, M/L and pharmaceutical related documents (e.g Price Certificates), which we either receive directly from the manufacturer/exporter directly or via third party agencies.

Depending on the market concerned, we evaluate the ‘optimum’ legalization route in terms of compliance, speed and cost to deliver the best possible service to our customers.

Typical applications with which we deal on a daily basis include:

  • FDA (Food and Drug Administration)
  • USDA (U.S. Department of Agriculture)
  • USPTO (United States Patent and Trademark Office)
  • FCC (Federal Communication Commission)

Please contact our Sales team on [email protected] to discuss your Regulatory Affairs Document needs.