We provide consultancy services to the Pharmaceutical & Medical Device Industries relying on our diversity of experience within the science, IT and regulatory fields, to provide a quality service which is both broad ranging and highly adaptable to your companies requirements and policies.

Our main service is the implementation and validation of pharmaceutical equipment & computer software in-line with US and EU regulations as set down by the FDA and EMEA. We also provide additional services including technical writing, documentation review, auditing and project management.

New regulations are continuous being introduced each year by the various global regulatory bodies and this makes it essential that your company maintains the highest levels of cGxP.

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