Lab Automate Technologies Inc

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Lab Automate Technologies Inc

🇺🇸 United States, New Jersey
2006
5-10 people
Manufacturer/Service Company
Lab Automate Technologies Inc is a specialized manufacturer and technology development company headquartered in Millburn, New Jersey, with an additional division in India. Founded in 2006, the company provides advanced automation and sterile manufacturing solutions for the pharmaceutical and biotechnology industries. As a contract manufacturer and authorized robotics system integrator for ABB, the firm focuses on accelerating drug development through precision engineering and custom laboratory automation. The company's core expertise lies in test automation systems for inhalation drugs and precision powder and liquid filling technologies. Key products include the A3G Automated Andersen Cascade Impactor, PRANA automated pMDI shakers and actuators, and CHAKRAVAT induction port and mouthpiece shakers. Their patented technology for automating cascade impactors is designed to significantly increase test throughput while reducing costs. Additionally, they offer aseptic transfer systems, automated manufacturing lines for autoinjector and pen assembly, and liquid handling workcells utilizing collaborative robot arms. Lab Automate Technologies Inc operates under GMP standards and holds ISO Class 0 certification for specific cleanroom solutions. Beyond equipment manufacturing, the company provides specialized services such as Aerodynamic Particle Size Distribution (APSD) testing, in-house mensuration for cascade impactors, and NGI induction port repair. With a team of experts possessing extensive experience in pharmaceutical testing systems, the company serves a global clientele including major industry players like AstraZeneca, Novartis, and Zydus.
OEM manufacturerOffers OEM services for customized brand manufacturing.
Product customizationOffers full customization for design and features.
Patented technologyHolds multiple product or process patents.
High-tech enterpriseRecognized as a high-tech or innovative enterprise.
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pMDI CONFIGURATION
0·0 reviews
The Next Generation Impactor or the NGI
0·0 reviews
The Next Generation Impactor or the NGI was invented to overcome the low productivity issues experienced by the Andersen Cascade Impactor. Traditionally it was thought that the ACI is impossible to automate. Many companies have switched to the NGI and as more and more people have begun using it, they too have experienced issues with it this then is not the answer that most people thought it would be. Typically users can get four to ten dose determinations per day per operator. The “A3G” is a third generation impactor that has all the advantages of the first and second generation impactors (the ACI and NGI) with none of the disadvantages of either technology. The picture shows the Next Generation Impactor. To increase productivity the number of individual parts has been reduced considerably. All of the cups shown in the bottom of the picture are integrated into a tray thus the operator has to handle a tray at a time. However the scope for automation is limited to solvent dispensing and sample collection. The washing is still all manual. The air passages are integrated into the body of the impactor (visible as large holes in the picture). They are difficult to clean and lead to drug accumulation and cross-over data errors. Further, the flight path of the aerosol particle is twice as long as in the ACI. This long path leads to droplet evaporation in case of the pMDI, and the errors tend to be biased towards fine particle fraction. To prevent droplet evaporation, scientists have to freeze/cool the NGI prior to use, making its productivity lower than claimed and the process expensive.
Andersen Cascade Impactor (ACI)
0·0 reviews
Andersen Cascade Impactor or ACI, has been the impactor of choice, and to date, for a good number of inhalation drugs on the market, the particle size distribution data submitted to the FDA has been obtained using the ACI. The manual ACI process greatly suffers from low productivity, typically two to four dose determinations per day and from operator induced data variability. Hence it takes years to generate the data and get regulatory approval from the FDA.
DUSA CONFIGURATION
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DPI CONFIGURATION
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NASAL CONFIGURATION
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🇺🇸 United States🇺🇸 United States
🇮🇳 India🇮🇳 India

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