EU Clinical Trials Register – FAQs

EU Clinical Trials Register

EU Clinical Trials Register . Page - 1. Sponsor Contact Information . Abbott Laboratories Ltd Abbott House, Vanwall Business Park, Vanwall Road, Maidenhead,

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EU Clinical Trials search

Note: The EU Clinical Trials Register user interface (UI) currently only supports English. 1.1. Basic search Click in the search field and enter a word or phrase.

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EU Clinical Trials Register Glossary | Search for …

EU Clinical Trials Register . Disclaimer: The explanations are provided for the benefit of public users of the system and to enhance general understanding of terms used.

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Guideline on pharmaceutical development of …

of January 2007, the “Paediatric Regulation” entered into force (Regulatio n EC No 1901/2006 of the European Parliament and of the Council, amending regulation EEC No 1768/92,

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Harmonised Technical Guidance for Using of …

Page 4 | 73 Version 1.0 – July 2015 1.4. This application is submitted in accordance with the following article in Directive 2001/83/EC as amended..... 26

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European Medicines Agency guidance for applicants …

European Medicines Agency Guidance for Applicants se eking scientific advice and protocol assistance EMA/4260/2001 Page 2/23 . Contents . Instructions for users .....3

Lipitor 51020 and 40mg Chewable Tablets PL 16051 …

UKPAR Lipitor 5mg, 10mg, 20mg and 40mg Chewable Tablets PL 16051/0006-9 1 LIPITOR 5MG, 10MG, 20MG AND 40MG CHEWABLE TABLETS

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RIAMET 20 MG/120 MG DISPERSIBLE TABLETS …

MHRA PAR – Riamet 20 mg/120 mg dispersible tablets (PL 00101/0957) - 1 - RIAMET 20 MG/120 MG DISPERSIBLE TABLETS (Artemether and lumefantrine) PL 00101/0957 . UKPAR . TABLE OF CONTENTS

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PDCO EMA Update AMK 13-06-2017

Lääkealan turvallisuus- ja kehittämiskeskus Structure • Background - Paediatric Regulation and PIPs • Dialogue with PDCO/EMA • Global interaction EMA / FDA

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