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APV/IPEC Europe Excipient Conference 2014  | CN 3128

An update on regulatory and application developments 23.09. - 24.09.2014 | Düsseldorf-Ratingen, Germany

Venue

Holiday Inn Düsseldorf Airport-Ratingen
Broichhofstr. 3
40880 Düsseldorf-Ratingen
Phone:+49 2102 456-0

Dear Colleagues,

The success of the excipient conferences jointly organised by APV and IPEC Europe in the last years motivated us to continue also 2014. This year we put together a program focusing on two major areas: regulation and application.
In the field of regulation we will give a broad view on excipient regulation in Europe, the USA and emerging countries and would like to discuss with the audience the impact on our business. Excipient suppliers are more and more in the focus of regulators and drug manufacturers. This is reflected in topics on supplier qualification, marketing authorization dossiers and excipient quality system standards. Application related topics of the conference will be on pediatrics, parenterals, biopharmaceuticals, Quality by Design and novel excipients.
With this selection of subjects we would like to cover the range of current hot topics and allow participants to discuss the topics with experts. There will be enough opportunities for networking and learning about different subjects to broaden our horizon in the area of pharmaceutical excipients.
On behalf of IPEC Europe and APV it will be a great pleasure for us to welcome you to the conference 2014.
Hubertus Folttmann (Board Member of APV and IPEC Europe) and Frank Milek (Chair to IPEC Europe)

Workshop programme for download

Target groups

This conference is intended for professionals working in
• development, manufacture and quality
• distribution and sales
• qualification of suppliers
• application and control
of pharmaceutical excipients for medicinal products.
The seminar is also intended for members of regulatory authorities and purchasing departments.

Objective

This event is designed to highlight current hot topics in the field of pharmaceutical excipients:
• Regulatory environment – key changes in Europe, USA and emerging countries
• Supplier qualification practice
• Excipients in marketing authorization dossiers
• Excipient quality system standards
• Excipients in pediatrics, parenterals and biopharmaceuticals
• Novel excipients
• Quality by Design

Registration fee

  Regular Fee Reduced Fee
1,490.00 € 1,360.00 €
incl. Workshop 1,790.00 € 1,660.00 €
All prices plus VAT

Organizer(s)

APV GmbH

Phone: +49 6131 97690
Fax: +49 6131 976969
E-mail: apv@apv-mainz.de
www: https://www.apv-mainz.de/apv/