Step by Step through Medical Device Law
Requirements for Germany and Europe
Step by Step through Medical Device Law
Köln / 02.07.2013
The seminar language will be English. It is also possible to pose questions in German.[more]
Köln / 02.07.2013
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Biosimilars 2014
Clinical topics, quality requirements & vigilance aspects
Biosimilars 2014
Frankfurt / 04.07.2013 - 05.07.2013
In this seminar you will get a thorough update on the regulatory guidelines and the development programmes (the EU, the USA and worldwide).[more]
Frankfurt / 04.07.2013 - 05.07.2013
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Market Access & Pricing in the Major EU Markets
Conference on cost pressure and the consequences for your business
Market Access & Pricing in the Major EU Markets
Frankfurt / 04.07.2013
This conference gives you tips on how you can successfully enter the EU markets with your pharmaceuticals[more]
Frankfurt / 04.07.2013
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Medical Writing in Pharmacovigilance
Medical Writing in Pharmacovigilance
Heidelberg / 09.07.2013 - 10.07.2013
DER Workshop für alle, die Dokumente in der Pharmakovigilanz verfassen, überprüfen oder freigeben![more]
Heidelberg / 09.07.2013 - 10.07.2013
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Marketing Authorisation in the CIS Countries/Russia
Focus: Russia, Belarus, Ukraine and Kazakhstan - also adressed: Azerbaijan, Mongolia, Uzbekistan, Armenia, Moldova, Georgia
Marketing Authorisation in the CIS Countries/Russia
Berlin / 22.08.2013 - 23.08.2013
Regulatory Affairs Know how - in this seminar you can discuss with local experts![more]
Berlin / 22.08.2013 - 23.08.2013
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Marketing Authorisation in the Balkan States
Albania, Montenegro, Macedonia, Bosnia & Herzegovina, Serbia and Kosovo
Marketing Authorisation in the Balkan States
Frankfurt / 03.09.2013
In this seminar you will get a thorough updat on the regulatory requirements (marketing authorisaton and maintenance) in Croatia, Montenegro, Macedonia, Bosnia, Serbia + Kosovo[more]
Frankfurt / 03.09.2013
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10th Conference on Marketing Authorisation
Conference at day 1: Regulatory challenges for 2014
10th Conference on Marketing Authorisation
Köln / 30.09.2013
EU challenges for regulatory affairs - expert meeting with speakers from various agencies and the industry[more]
Köln / 30.09.2013
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10th Conference on Marketing Authorisation
Seminar at day 2: Mutual Recognition Procedure (MRP) & Decentralised Procedure (DCP) - regulatory strategy
10th Conference on Marketing Authorisation
Köln / 01.10.2013
Serminar regarding MRP + DCP - accelaration and delaying factors / Mutual Recognition Procedure + Decentralised Procedure - beschleunigende und verzögernde Faktoren im Verfahren[more]
Köln / 01.10.2013
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Medical Writing Essentials
Focus: The Clinical Study Report and more
Medical Writing Essentials
Frankfurt / Offenbach / 14.10.2013 - 15.10.2013
Medical Writing Essentials[more]
Frankfurt / Offenbach / 14.10.2013 - 15.10.2013
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Marketing Authorisation for Human Medicines in Latin America
Brazil, Mexico, Argentina, Venezuela, Colombia, Chile, Peru
Marketing Authorisation for Human Medicines in Latin America
Frankfurt / Offenbach / 14.10.2013
Arzneimittelzulassung in Lateinamerika - Kompaktseminar mit lokalen Experten[more]
Frankfurt / Offenbach / 14.10.2013
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Therapeutic Antibodies
Preclinical & clinical development and marketing authorisation
Therapeutic Antibodies
Frankfurt / 15.10.2013
Join this seminar for an update on international regulatory framework for originator and biosimilar antibodies.[more]
Frankfurt / 15.10.2013
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Marketing Authorisation in ASIA, Australia & New Zealand
Here you can create a course tailored to your needs!
Marketing Authorisation in ASIA, Australia & New Zealand
Frankfurt / 15.10.2013 - 18.10.2013
China, Hong Kong, Indonesien, Singapur, Thailand, Korea, Malaysia, Philippinen, Vietnam, Taiwan, Australia + New Zealand will be addressed in the seminar.[more]
Frankfurt / 15.10.2013 - 18.10.2013
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Marketing Authorisation in North & South Africa
Regulatory Update - The Maghreb Countries & South Africa
Marketing Authorisation in North & South Africa
Frankfurt / 30.10.2013
This seminar gives you a thorough update on the regulatory requirements in Tunisia, Algeria, Morocco and South Africa (marketing authorisation and maintenance).[more]
Frankfurt / 30.10.2013
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The Centralised Procedure
The Centralised Procedure for NCEs, generics and OTC drugs
The Centralised Procedure
Bonn / 08.11.2013
The Centralised Procedure can be accessible for NCEs, Generics and OTC products - in this seminar you will get practical hints regarding the dossier and the procedure.[more]
Bonn / 08.11.2013
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Update Biomarker
Development, Validation and Marketing Authorisation in EU & USA
Update Biomarker
Stuttgart / 06.12.2013
Update on regulatory requirements for development and marketing authorisation of therapeutic antibodies.
[more]
Stuttgart / 06.12.2013
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