Reliable product protection for every pharmaceutical process in light of the new version of Annex 1, which came into force in August 2023, many pharmaceutical manufacturers are facing the question whether they must invest in new equipment. However, in many cases upgrades are a good alternative so Pharma Egypt for Engineering is the best choice to make this upgrade. According to the revised EU GMP Annex 1, sterile production must take place under RABS or isolator conditions to ensure maximum product and operator protection.

Glove ports are needed to avoid opening of glass doors, for example to change settle plates for environmental monitoring or in the case of manual interventions through the glove ports.Depending on the individual production and filling facility, an ORABS may be the right solution to separate and protect aseptic production in a Class B environment.