ARVO Annual Meeting
May 3-7, 2026
Denver, USA
https://www.arvo.org/annual-meeting
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May 3-7, 2026
Denver, USA
https://www.arvo.org/annual-meeting
June 22-25, 2026
San Diego, USA
https://convention.bio.org/
July 6-9, 2026
Lisbon, Portugal
https://www.controlledreleasesociety.org/events/crs-2026-annual-meeting-exposition
July 8-10, 2026
Bangkok, Thailand
https://www.cphi.com/sea/en/attend/attend/why-attend.html
October 6-8, 2026
Milan, Italy
https://www.cphi.com/europe/en/exhibit/book-your-stand-milan.html
October 29-30, 2026
Boston, USA
https://poddconference.com/
November 9-11, 2026
Cologne, Germany
https://informaconnect.com/bioeurope/
May 22-24, 2025
Vienna, Austria
September 29 – October 1, 2025
Berlin, Germany
https://ipls.online/events/
October 28-30, 2025
Frankfurt, Germany
https://www.cphi.com/europe/en/home.html
February 5-6, 2026
London, UK
https://pharma-synergy-conference.com/pharmasynergy-2026/
March 2-3, 2026
Lisbon, Portugal
https://www.raucon.com/euro-plx/euro-p-l-x-90
March 23-25, 2026
Lisbon, Portugal
https://informaconnect.com/bioeurope-spring/
March 23-26, 2026
New York City, USA
https://dcatweek.org/
March 23-26, 2026
Prague, Czech Republic
https://worldmeeting.org/
March 24-27, 2026
Munich, Germany
https://analytica.de/de/muenchen/
The contract applies to Southeast Asia, including China, Eastern Europe, Russia and some Western European countries. The agreements contain down payment payments of up to € 10 million, license payments in the double-digit percentage range, and an exclusive delivery agreement for AMW. The partner company will carry out further clinical developments for the contract area.
read moreNr.ISO Certificate: Q21-13.07.84140.001
Validity: from 07.10.2013 to 06.10.2016
Scope: Manufacture, quality control, quality assurance and distribution of medical devices in plaster form
Applied standard(s):
EN ISO 13485: 2012/AC: 2012
Medical devices
Quality management systems
Requirements for regulatory purposes
Type of inspection: General GMP inspection in accordance with Section 64 of the German Medicines Act (AMG), the provisions of the German Medicines and Drug Manufacturing Ordinance (AMWHV) and the EC-GMP Guide for the Acceptance of the New Manufacturing Rooms of AMW GmbH for the Production of Transdermal Systems, Verification of Systems for the Production of Clinical Test Samples and Manufacture of Market Goods for The Products: Transdermal Systems and Implants and for obtaining manufacturing authorisation for Market Goods.
read moreGeneral GMP inspection in accordance with Section 64 of the German Medicines Act (AMG), the provisions of the German Medicines and Drug Manufacturing Ordinance (AMWHV) and the EC-GMP Guide for the Acceptance of the New Manufacturing Rooms of AMW GmbH
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