Automatic Ampoules Inspection

EIPICO uses State-Of-The-Art vision inspection equipment for the detection of any contaminants.

A gloved hand holds a vial filled with liquid

Each ampoule passes parallel to testing stations, the measured values are documented in reports and charts. The system is validated, coping with 21CFR11 (Title 21 of the Code of Federal Regulations) established by the United States Food and Drug Administration (FDA) on Electronic Records and Electronic Signatures (ERES). Part 11, Which defines the criteria under which electronic records and electronic signatures are considered trustworthy, reliable, and equivalent to paper records-Audit Trail-cGMP and GAMP5.

The rejected vials/ampoules are then transferred to a rejection station from where they are ejected out of the machine. The correct vials/ampoules are accepted and transferred to the collection station where they are collected by a collection tray.

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STERILE PRODUCTS AREA

Are areas that have HEPA filtration to remove particles from the air. They are used for manufacturing where high levels of cleanliness and sterility are required.

EIPICO OPHTHALMOLOGY

EIPICO is ranked Number 1 in the Egyptian Ophthalmic Market, by Units.

PRIMARY PACKAGING MATERIALS

EIPICO focuses on its products quality, hence holding product filling and packaging process inhouse is a corner stone of delivering products of high-quality standards to the community.