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Iniciación a Asuntos Regulatorios
El área de registros para no expertos

Iniciación a Asuntos Regulatorios

Madrid / 22.02.2012

Iniciación a Asuntos Regulatorios[mehr]

Madrid / 22.02.2012
IP Biotech Pharma
Part I

IP Biotech Pharma

London / 27.02.2012

IP Days Pharma - Biotech: What you need to know![mehr]

London / 27.02.2012
IP Biotech Pharma
Part II

IP Biotech Pharma

London / 28.02.2012

IP Days Pharma - Biotech: What you need to know![mehr]

London / 28.02.2012
Variations Conference
Variation application & procedures

Variations Conference

Köln / 28.02.2012

International conference on the Variations Regulation (grouping, worksharing), the impact of the pharma package and variations in the eCTD format[mehr]

Köln / 28.02.2012
Supplementary Protection Certificates

Supplementary Protection Certificates

London / 29.02.2012

Supplementary Protection Certificates[mehr]

London / 29.02.2012
Variations Conference
Quality related variations

Variations Conference

Köln / 29.02.2012

Quality related variations - classification, design space possibilities and the new task "post approval change management protocols"[mehr]

Köln / 29.02.2012
The Patenting of Biotech and Pharmaceutical Inventions

The Patenting of Biotech and Pharmaceutical Inventions

London / 01.03.2012 - 02.03.2012

The Patenting of Biotech and Pharmaceutical Inventions[mehr]

London / 01.03.2012 - 02.03.2012
mAb Biosimilars 2012
Monoclonal antibodies as biosimilars

mAb Biosimilars 2012

Frankfurt / 01.03.2012 - 02.03.2012

Seminar regarding the new guideline on similar biological medicinal products containing monoclonal antibodies[mehr]

Frankfurt / 01.03.2012 - 02.03.2012
Marketing Authorisation in the Middle East, Africa, Turkey, Australia and New Zealand
Marketing Authorisation/Arzneimittelzulassung im Nahen Osten, Afrika, Türkei, Australien, Neuseeland

Marketing Authorisation in the Middle East, Africa, Turkey, Australia and New Zealand

Frankfurt / 05.03.2012 - 07.03.2012

Current challenges in regulatory affairs - addressed by experts with local know how[mehr]

Frankfurt / 05.03.2012 - 07.03.2012
Medical devices: Marketing authorisation in the Middle East & North Africa (MENA)
Target countries: United Arab Emirates, Saudi Arab, Egypt and Jordan

Medical devices: Marketing authorisation in the Middle East & North Africa (MENA)

Mannheim / 07.03.2012

Medical devices: Marketing authorisation in the Middle East & North Africa (MENA)[mehr]

Mannheim / 07.03.2012
Regulatory intelligence: come può influire sul processo autorizzativo di un medicinale

Regulatory intelligence: come può influire sul processo autorizzativo di un medicinale

Milano / 07.03.2012

Regulatory intelligence: come può influire sul processo autorizzativo di un medicinale[mehr]

Milano / 07.03.2012
Scadenza 02.07.2012! Trasmissione elettronica all'EMA delle informazioni sui medicinali

Scadenza 02.07.2012! Trasmissione elettronica all'EMA delle informazioni sui medicinali

Milano / 08.03.2012

Scadenza 02.07.2012! Trasmissione elettronica all'EMA delle informazioni sui medicinali[mehr]

Milano / 08.03.2012
International R&D - Implications of Employee Inventions

International R&D - Implications of Employee Inventions

Stockholm / 09.03.2012

International R&D - Implications of Employee Inventions[mehr]

Stockholm / 09.03.2012
Regulatory Affairs India
Marketing Authorisation in India/Arzneimittelzulassung in Indien

Regulatory Affairs India

Frankfurt / 14.03.2012

Current challenges in regulatory affairs - addressed by experts with local know how[mehr]

Frankfurt / 14.03.2012
Medical Device: istruzioni per l'uso

Medical Device: istruzioni per l'uso

Milano / 14.03.2012 - 15.03.2012

Medical Device: istruzioni per l'uso[mehr]

Milano / 14.03.2012 - 15.03.2012
Regulatory Affairs China
Marketing Authorisation in China/Zulassung in China

Regulatory Affairs China

Frankfurt / 15.03.2012

Current challenges in regulatory affairs - addressed by experts with local know how[mehr]

Frankfurt / 15.03.2012
The Practice of multi-jurisdictional Patent Litigation

The Practice of multi-jurisdictional Patent Litigation

Amsterdam / 18.03.2012 - 19.03.2012

The Practice of multi-jurisdictional Patent Litigation[mehr]

Amsterdam / 18.03.2012 - 19.03.2012
Litigating Standard-Essential Patents

Litigating Standard-Essential Patents

Amsterdam / 20.03.2012

Litigating Standard-Essential Patents[mehr]

Amsterdam / 20.03.2012
China IP 2012
Update on Strategy, Protection, Enforcement - Focusing on patents, utility models and trade marks -

China IP 2012

Zürich-Opfikon / 22.03.2012

China IP 2012[mehr]

Zürich-Opfikon / 22.03.2012
Jurisprudence actuelle de l'OEB: chimie et biotechnologie

Jurisprudence actuelle de l'OEB: chimie et biotechnologie

Paris / 23.03.2012

Jurisprudence actuelle de l'OEB: chimie et biotechnologie[mehr]

Paris / 23.03.2012
U.S. Patent Reform
Consequences for European Practitioners

U.S. Patent Reform

München / 03.04.2012 - 04.04.2012

U.S. Patent Reform[mehr]

München / 03.04.2012 - 04.04.2012
Il Time to Market di un medicinale
Attività, pianificazione e responsabilità delle funzioni aziendali coinvolte

Il Time to Market di un medicinale

Milano / 03.04.2012

Il Time to Market di un medicinale[mehr]

Milano / 03.04.2012
Vigilanza e sorveglianza dei Dispositivi Medici
Obblighi e responsabilità degli attori coinvolti

Vigilanza e sorveglianza dei Dispositivi Medici

Milano / 04.04.2012

Vigilanza e sorveglianza dei Dispositivi Medici[mehr]

Milano / 04.04.2012
La brevetabilité des inventions en biotechnologie

La brevetabilité des inventions en biotechnologie

Paris / 12.04.2012

La brevetabilité des inventions en biotechnologie[mehr]

Paris / 12.04.2012
International Patent Conference 2012

International Patent Conference 2012

München / 17.04.2012 - 18.04.2012

International Patent Conference 2012[mehr]

München / 17.04.2012 - 18.04.2012
English writing and reviewing in regulatory affairs
Package leaflet and further documents

English writing and reviewing in regulatory affairs

Frankfurt / Offenbach / 18.04.2012

Seminar on writing, editing and proofreading of regulatory documents[mehr]

Frankfurt / Offenbach / 18.04.2012
Patent Law in the Russian Federation
The rules, the changes and recent developments

Patent Law in the Russian Federation

München / 19.04.2012

Patent Law in the Russian Federation[mehr]

München / 19.04.2012
Trademark Administration
A practical guide on the CTM and the Madrid System

Trademark Administration

Alicante / 25.04.2012

Trademark Administration[mehr]

Alicante / 25.04.2012
FDA: Marketing Authorisation in the USA
Update on the IND, NDA & BLA procedures

FDA: Marketing Authorisation in the USA

Köln / 25.04.2012

Details on the FDA drug registration and communication with the authority[mehr]

Köln / 25.04.2012
12th International Trademark Conference 2012

12th International Trademark Conference 2012

Alicante / 26.04.2012 - 27.04.2012

12th International Trademark Conference 2012[mehr]

Alicante / 26.04.2012 - 27.04.2012
ExpertFORUM Labeling/Product information
1st day: Product information - challenges for 2012

ExpertFORUM Labeling/Product information

Bonn / 07.05.2012

International FORUM Conference on the current challenges with regard to labeling + SmCP[mehr]

Bonn / 07.05.2012
ExpertFORUM Labeling/Product information
2nd day: Electronic submission of the product information - XEVPRM

ExpertFORUM Labeling/Product information

Bonn / 08.05.2012

Seminar with detailed information on EVMPD and XEVPRM - THE task for 2012! [mehr]

Bonn / 08.05.2012
PCT Formalities Course
Guide to the Formal Requirements

PCT Formalities Course

Copenhagen / 09.05.2012 - 10.05.2012

The purpose of this basic seminar is to inform the participants how to prepare an international application for filing under the PCT and subsequently monitor the consecutive procedural steps, timelimits and payment of fees in the...[mehr]

Copenhagen / 09.05.2012 - 10.05.2012
Stratégies de protection de l'innovation
Du dépôt au litige - retours d'expériences

Stratégies de protection de l'innovation

Paris / 09.05.2012

Stratégies de protection de l'innovation[mehr]

Paris / 09.05.2012
IL RUOLO DELLA STATISTICA NELLA RICERCA CLINICA

IL RUOLO DELLA STATISTICA NELLA RICERCA CLINICA

Milano / 10.05.2012

IL RUOLO DELLA STATISTICA NELLA RICERCA CLINICA[mehr]

Milano / 10.05.2012
LO SVILUPPO DELLA FARMACOVIGILANZA NELL'UE
Impatto della nuova normativa sulle aziende farmaceutiche

LO SVILUPPO DELLA FARMACOVIGILANZA NELL'UE

Milano / 10.05.2012

LO SVILUPPO DELLA FARMACOVIGILANZA NELL'UE[mehr]

Milano / 10.05.2012
Marketing authorisation in Japan
Drug marketing authorisation in Japan - MHLW, PMDA, KIKO

Marketing authorisation in Japan

Frankfurt / 14.05.2012

Marketing authorisation in Japan - the precondition for a successful market access[mehr]

Frankfurt / 14.05.2012
The Decentralised Procedures - an update for 2012
MRP & DCP

The Decentralised Procedures - an update for 2012

Frankfurt / 15.05.2012

Seminar on current challenges in MRP and DCP and the upcoming tasks for the CMDh[mehr]

Frankfurt / 15.05.2012
Step by Step through Medical Device Law
Requirements for Germany and Europe

Step by Step through Medical Device Law

Köln / 03.07.2012

Das Medizinproduktegesetz wird in diesem Seminar in englischer Sprache verständlich erläutert.[mehr]

Köln / 03.07.2012
Marketing Authorisation in the CIS Countries
Focus: Russia, Belarus, Ukraine, Kazakhstan

Marketing Authorisation in the CIS Countries

Berlin / 27.08.2012

Regulatory Affairs Know how - here you can discuss with local experts![mehr]

Berlin / 27.08.2012
Marketing Authorisation in the Balkan States
Albania, Croatia, Montenegro, Macedonia, Bosnia & Herzegovina, Serbia and Kosovo

Marketing Authorisation in the Balkan States

Frankfurt / 04.09.2012

Seminar on the regulatory requirements in Croatia, Montenegro, Macedonia, Bosnia, Serbia + Kosovo[mehr]

Frankfurt / 04.09.2012
Successful Medical Writing

Successful Medical Writing

Frankfurt / 25.09.2012 - 26.09.2012

In-depth training in general writing and data presentation skills, and specifically in the kinds of documents most frequently encountered in clinical research.[mehr]

Frankfurt / 25.09.2012 - 26.09.2012
Marketing Authorisation in Asia
China, Hong Kong, Indonesien, Singapur, Thailand, Korea, Malaysia, Philippinen, Vietnam, Taiwan

Marketing Authorisation in Asia

Frankfurt / 17.10.2012 - 18.10.2012

Update on the regulatory framework in Asia with a focus on China, Hong Kong, Indonesia, Korea, Malaysia, Philippines, Singapore, Taiwan, Thailand, Vietnam.[mehr]

Frankfurt / 17.10.2012 - 18.10.2012
Marketing Authorisation in Latin America
Brazil, Mexico, Argentina, Chile, Peru and Colombia

Marketing Authorisation in Latin America

Frankfurt / 11.12.2012

Arzneimittelzulassung in Latein Amerika - Kompaktseminar[mehr]

Frankfurt / 11.12.2012
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