Pharmaceutical purified water equipment appearance, structure and material inspection

Pharmaceutical purified water equipment appearance, structure and material inspection 1, pharmaceutical purified water equipment machine signs and logo complete, touch screen interface should also be prepared in accordance with the requirements of the contract, control panel must be in English and Chinese control or contract designation language.
2, all parts of the machine must be fully installed, internal and external surface polishing consistent, smooth, easy to clean, do not shed particles, do not hide contaminants, do not pollute drugs, no burrs, rust, scratches, bumps, welds smooth, no welds Black scar, painted surface complete, uniform, bright, colorless spot, drip hanging, shedding phenomenon, installation door neat and beautiful, no deformation, flexible switch, including control box door around the silicone pad, no welding spot in the box, no burrs around, the whole machine clean and bright.
3, pharmaceutical purified water equipment all operating buttons, switches, indicators and other components must be clearly identified, all rotating components such as motors, hand wheels, turntables, adjustment knobs must identify the direction, all external media such as power supply, control line plugs, in and out of water pipes, compressed air, vacuum and other interfaces must identify and indicate specifications, such as voltage, compressed air pressure, vacuum and dosing.
have eye-catching electrical ground markings and other operational safety on the machine, such as beware of burns, careful rolling, etc.
4, the machine each operation, transmission part of the commissioning must be in accordance with the provisions of refueling lubrication, the machine lubrication site must have lubrication point identification.
non-stainless steel part of the surface of the machine must be rust-proof treatment, each drive, fasteners must be located accurately, firmly, no loose.
5, pharmaceutical purified water equipment parts of the material must meet the requirements, direct contact with the drug parts should be 316L stainless steel production (or contract specified material), the use of arc welding, welding must be polished treatment, containers and equipment containing materials must be polished, polished inner surface up to 0.3, outer surface 0.8, silicone, Tevron, cloth bags and other materials should meet the requirements of GMP standards (inspection material certification documents).
6, the whole machine electrical lines, process lines must be laid out reasonably, installed in an orderly manner, each wire hole needs to have rubber sheaths, wires need to be wired, connectors need to meet electrical requirements, lines need to be labeled, each electrical parts must be labeled.
7, pharmaceutical purified water equipment specifications of accessories, spare parts, molds must indicate specifications, and the material must meet their respective quality requirements, before packing inspection and acceptance after cleaning oil, packaging after the name, specifications, quantity schedule.