Integrated Drug Development Solutions
Dosage Development
Dosage Development
Bioanalytical Development
Phase I–Phase IV
Bioanalytical development
Project Development
Project Management
Aizant provides cGMP manufacturing services for clinical trial materials (CTM) and niche commercial supplies for non sterile dosage forms. Our facility offers flexibility and variety in batch sizes as well as processing requirements. The pilot facility is located in the same facility as our product development labs. We have additional facilities to handle development and manufacturing of potent compounds.

Equipment and process capabilities:
  • Direct tablet compression
  • Fluid bed processing (granulation, drying, coating)
  • High shear granulation
  • Dry granulation
  • Tablet coating
  • Automated capsule filling (powder, granules, pellets)
  • Microencapsulation
  • Low humidity / moisture requirements
Quality