PHARMACY

May 15 2020

European pharmaceutical regulatory affairs experts – Pharma-EU, s, pharma services.

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Pharma-EU.com: Pharmaceutical Regulatory Solutions for the European Union

Pharma services

Consultations with patients regarding the package information leaflets. Guaranteed acceptance across the EU for National, MRP, DCP and CPs.

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Previously tested PILs can be used to support other PILs to create readability testing exemptions.

Pharma servicesReadability Testing of Package Information Leaflets and Bridging for the Generic Industry – download (285 kB)

European Regulatory Pharmaceutical Consulting Services

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We can reformat and submit your pharmaceutical’s dossier to any member state in eCTD or CTD format.

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Our regulatory managers have proven their experience in coordinating and completing European procedures.

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We can work on-site as well as off-site to coordinate variations and maintenance of existing licenses.

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Expert support Module 1 for centralized, decentralized, mutual recognition and national procedures.

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We translate medical documents to all European languages using our network of certified medical translators.

Preferred Readability Testing Providers for:

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Content: (c) 2008 Pharma-EU, s.r.o.

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