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


Posted On Aug 27 2018 by

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

Pharma consultants

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

Pharma consultants

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

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

European Regulatory Pharmaceutical Consulting Services

Pharma consultants

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

Pharma consultants

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

Pharma consultants

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

Pharma consultants

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

Pharma consultants

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

Preferred Readability Testing Providers for:

Pharma consultants

Pharma consultants

Pharma consultants

Pharma consultants

Pharma consultants

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

Pharma consultants


Last Updated on: August 27th, 2018 at 5:13 pm, by


Written by admin


Leave a Reply

Your email address will not be published. Required fields are marked *