AVT delivers tailored, GMP-compliant industrial-scale production of specialty excipients. We provide comprehensive technical services, including customized product R&D, lab-scale testing, pilot-scale testing, process validation, and product registration. These services cater to development needs ranging from grams to hundreds of kilograms.
AVT has developed and registered multiple injectable-grade excipients, accumulating extensive experience in process development and quality research. Our seasoned registration team is well-versed in excipient regulatory requirements, enabling efficient product registration.
We are equipped with advanced standard chemical labs and research equipment capable of complex chemical process development. Our specialized analytical instruments include UV, CAD, ELSD, GC, and RID . Additionally, we utilize an advanced eGMP system for quality management to ensure product quality and the batch-to-batch consistency.
Dedicated to parenteral grade high-end excipients since 2007.
1200㎡ RD area (small scale + pilot scale)
5000㎡ cGMP plant area (commercial scale)
Rich experience in product DMF registration in FDA
18 patents in complex formulation
Reach 1700+university research institute Reach 1800+ biotech/biopharma companies