From April 17th to 19nd, the 57th (Spring) National Pharmaceutical Machinery Exposition and China International Pharmaceutical Machinery Exposition was held in Changsha. The products and high-end integrated engineering solutions that covered the whole drug life cycle had been introduced, attracting nearly a thousand participants to stop and focus.
In the exhibition, many production lines and solutions were presented, such as AUSTAR fluid technology system and laboratory one-stop solution. Guests came in an endless stream, they were warmly greeted and patiently answered.
AUSTAR is dedicated to the construction of intelligent factories, and integrates its own equipment and validation capabilities to provide a total solution. The exhibition shows many applications such as BMS&EMS, API process control and traditional Chinese medicine process control.
Integrated solution is provided in the field of containment technology, thanks to the successful integration of automation control technology, isolation technology and powder processing technology. AUSTAR works together with ROTA, BE Company and GF Company to provide efficient solutions including cleaning, sterilization, filling, sealing, leaking test and appearance integrity detection.
For API industry, we provide products and service for the pharmaceutical enterprises of upstream and downstream process system design which could meet customers' requirements of different production line, including biological fermentation, extraction, chemical synthesis and related supporting system, etc., helping customers to achieve high standards of technological process.
Cooperation with international first-class experienced technology R&D team, AUSTAR helps to implement solid preparation engineering services and technical support, equipped with core products including Alexanderwerk granulating equipment, Pharmagel soft capsule filling equipment, Ackley printing machine and Thomas coating machine, etc. In addition, we also have industry-leading PAT wet granulating production line, equipped with WIP cleaning device using batch management, traceability data of production process, through AUSCON self-control operation system, the whole process conforms to FDA, EMA, and WHO requirements.
AUSTAR professional team closely follows the latest global pharmaceutical regulatory guidelines for interpretation and transformation. During the exhibition, ASTM E2500 Application Guide and EU GMP/GDP regulation supplement were published, which caused a rush of books. For a moment, the new validation concept was discussed and became a hot topic.
AUSTAR will practice its mission to keep forward, looking forward to the next time!