Business

The integration of services and software to provide competitive compliance, quality advocacy and thought leadership.

Provides consulting services in the scientific and regulatory aspects of a wide range of medical devices with particular expertise in the areas of in vitro diagnostics and biotechnology-based products.

Regulatory affairs consultancy in Poland and EU (MRP, DCP, national, medical devices, food supplements, and scientific dossier consultation).

A UK based company providing regulatory affairs consultancy and patient information leaflet user testing to the pharmaceutical industry.

Specializing in regulatory strategy development, preparation, and review of regulatory submissions.

Generic downloadable documents that are cGMP compliant.

Offers a full range of validation, compliance and technical services for the pharmaceutical, biotechnology and medical device industries.

They provide contract and consulting services in the following areas: validation and technical services (IQ OQ PQ protocols and validation master plans VMP), quality systems development, laboratory services, environmental monitoring, and water testing.

Worldwide validation, quality, compliance, and production services for the medical device, pharmaceutical, nutraceutical, and biotechnology industries.

Validation and regulatory consulting services for the pharmaceutical, biotechnology, and medical device industries.

Medical device regulatory affairs

Provides services to small and mid-sized pharmaceutical and device companies including biotechnology in the areas of preclinical, clinical, CMC and regulatory.

Provides consulting services in the areas of patent, regulatory affairs, marketing research, and QA/GMP documentation for small to medium size pharmaceutical companies.