1930 | Inception of E.M.A. (Emboutissage Métallique Appliquée) at Saint Cloud (Paris). Manufacturing of aluminum seals for various industrial applications. |
1950 | Development of Aluminum Crimp Caps for pharmaceutical containers (injection vials, infusion bottles, cartridges, etc.) |
1974 | Introduction of the « Push-Off » product range;![]() Manufacturing of combined Aluminum/ Polypropylene caps. |
1987 | Transfer of the production facility from Saint Cloud (Paris) to Lailly en Val (Orleans) to improve the production layout. |
2003 | First ISO 9001 certification. |
2006 | The company is renamed EMA Pharmaceuticals. The production becomes solely focused on seals for pharmaceutical applications. |
2008 | Enhancement of QA lab equipment, introduction of laminar flow equipment in production |
2009 | Registration of a type III DMF for the Push-Off product range at the FDA. |
2011 | Introduction of Clean Room technique, for the assembling of the « Push-Off » product range. |
2013 | Launch of EMA CLEAN-CERTIFIED CAPS, ensuring a low level of microbiological and particulate contamination before sterilization. |