The process of manufacturing Eye Drops is the most complex out of all the medicines as the scope of contamination is the highest here thus needing the most sophisticated equipment, personnel and sterile environment.
The production of the eye drops sterile preparations is carried out in clean areas, entry to which is made through airlocks for personnel and/or for equipment and materials.
Clean areas are maintained to an appropriate standard of cleanliness and supplied with air passed through High-efficiency particulate air (HEPA) filters which maintain a specific air quality of required efficiency.
The clean room environment uses 316 SS containers with digital monitors and sensors for temperature, time and humidity control of the mechanical process making the clean room facility of Class 100 specification.
After the preparation of each batch it gets tested by a third party NABL Accredited Laboratory before being introduced in the market.
