EMA Pharmaceuticals’ Clean-Certified Caps ensure a low level of microbiological and particulate contamination before their sterilization and use within the aseptic process. This is an important issue for all pharmaceutical laboratories sealing sterile product as an aseptic process: They have to ensure the safe finishing of their sterile product by using clean and sterilized crimp caps (according to EU GMP, annex 1).
Clean-Certified Caps are specifically processed caps, ensuring a controlled, low content of particulate and bioburden contamination before sterilization. According to the customers’ production process, Clean-Certified Caps can be provided in ready-to-be-sterilized or ready-to-be-used versions, providing a validated irradiation treatment on-demand.
The launch of this new service range is accompanied by the redesign of the company’s Website allowing pharmaceutical companies to choose the best possible sealing solution for their needs.
