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| | | Objectives- Implementation of GMP in an excipient manufacturing site
- Qualification and auditing of suppliers
- Analytical data and certificates of analysis for excipients
- The European Pharmacopoeia’s General Methods Modernisation Programme
- USP – Strategies and Opportunities for Excipient Standard Setting
- Particulate matter in pharmaceutical starting materials and drug products
- Regulatory and technical challenges for excipients in parenteral formulations
- Formulation topics
Here you can download the program as a PDF file
or simply click on the picture | |
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| WorkshopsThis year again, we offer you to arrange your individual conference focus (Workshops will run in parallel two times. You will have the opportunity to participate in 2 workshops.)
- How to implement appropriate GMPs in an excipients manufacturing site
– "What brings you from ISO 9001 to "Excipient GMP"
- How to use IPEC GMP principles to manage suppliers
– "The use IPEC Guidelines in qualification and auditing of excipient suppliers"
- Analytical data and COAs of suppliers
– "How to enable pharma industry to outsource excipient testing to suppliers"
Connect and collaborate:
Don't miss this opportunity to meet with colleagues and potential business partners throughout the industry. Just click on the link and register directly online: Registration
We are looking forward to welcoming you in Cologne! | |
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| Table Top Presentation and Sponsoring OpportunitiesTake the opportunity to present your company, products and services to a truly focused target market. Here you can reach everyone dealing with excipients without wastage.
For detailed information about exhibiting and the different sponsoring options, please go to our website www.apv-mainz.de or contact Antonia Herbert, ah@apv-mainz.de | |
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| | | The International Pharmaceutical Excipients Council Europe "The future of excipients is in our hands"
http://ipec-europe.org | |
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