High-end customization, cloud monitoring Appearance, software function, arithmetic requirement, sample rack and whole machine design can be customized, and complete application solutions can be matched to meet application requirements
We can build a “Food and Drug Intelligent Supervision Platformto effectively supervise the production, circulation and use of food and drug
Cloud service-intelligent regulatory platform.
It is suitable for sealing integrity testing of pharmaceutical packaging to prevent moisture, oxygen, and microorganisms from contaminating products. Medicines: bottled, bagged, boxed, ampoules, vials, cartridges, prefilled needles (PFS), (BFS), (FFS), etc.
Spray cans: plunger spray cans; bag-lined spray cans; "energy jacket" spray cans; flexible tube spray cans.
The Model NBC-5150 can confirm the class of the clean room and print out the test results quickly, and meets ISO 14644 requirements. The instrument measures the no. of particles in 8 particle size channels simultaneously, with 5000 samples record storage. It is widely used in measuring particles in clean rooms and in evaluating the quality of indoor air. It also used for testing the performance of HEPA filters. It has a Stainless Steel Housing. It is very Portable.
※ It can't directly illuminate to a person's skin, especially a person's eyes;
※ Do not use your hand to directly contact with the tube;
※ Please wear sterile gloves before using and use alcohol to wipe the quartz tube;
※ Please contact the manufacturer in time of use;
The freezing point osmometer FPOSM-V2.0 produced by our company with independent research and development is in accordance with Raoul freezing point theory, based on the solution freezing point declined value proportional to the solution molar concentration, using high sensitivity of temperature-sensing element, to measure the freezing point of different solutions, so as to derive the osmotic pressure molar concentration. This theory has been widely used for the test and research of osmotic pressure molar concentration in the fields such as pharmaceuticals,pharmaceutical analysis, biological and food therapy
Capsule filters are produced using pleated processing. Their structure is impact and filter area is large, applicable to filter solutions that have slow flow rate and large volume. Capsule filters are sealed by means of melting, free from glues and adhesives and therefore will not contaminate filtrate. They will experience 100% integrity test, purified water washing, and pressure test before delivery. Materials of capsule filters are selectable.
The respirator filter is designed for the sterilization purposes when material pot gas exchange of the pharmaceutical industry, food industry. The vent of the material pot and the storage pot is separated by the filter, and the gas in the pot can be discharged smoothly, and the microorganisms and particulate of outside can not enter the inside. The filter is manufactured according to GMP standard. Filter selection of hydrophobic PTFE membrane, filtration accuracy of 0.01um for a variety of bacteria and phage to 99.9999% filter. This filter can do bubble point test, also be carried out online steam disinfection.
TA-2.0 Total organic carbon (TOC) is developed on the basis of the original offline total organic carbon analysis instrument, which can meet both online and offline test modes for the users. And 3 points can be online measured switching one by one, so the application is more extensive, which can completely meet various on-site use requirements for the customers, thus greatly reducing the on-line monitoring implementation cost for the customers.
Filters are made of Micro series hydrophilic asymmetric sulfonated PES. They have universal chemical compatibility, pH range 3~11. They feature large throughput and long service life, applicable to bio-pharmacy and other fields. Before delivery, each cartridge has experienced 100% integrity test, to ensure product filter efficiency. NSS cartridges are endurable to repeated online steam or high-pressure disinfection, meeting asepsis requirements of new version GMP.
The bag integrity tester produced by Beijing Neuronbc,:BGT-120 is based on the pressure drop test principle. The method is based on the program of ASTM F2095-01, which compliance with GAMPs and FDA 21 CFR Part 11. with authority management and electronic signature, value support, including IQ, OQ, PQ and SOP.
To meet the requirements of the new version of GMP, our company has carried out independent research and development and designed the NEH series of electronic heater jacket; The instrument is composed of high performance composite heating material and control unit, and it has been widely used in biotechnology, pharmaceutical and electronics and other fields.
Sterility test pump based on the principle of membrane filtration. The pump give positive pressure transmit liquid sample to the canister and filtered under positive pressure. After filtration, the filter membrane is washed to remove the antimicrobial agent of the product, and then the culture medium is filled in the filter to check whether the sample contains bacteria