Clinical trials manufacturing
SEPS Pharma has state-of-the art cleanroom facilities for GMP (Good Manufacturing Practice) compliant clinical supply manufacturing, packaging and labeling of liquid, semi-solid and solid dosage forms on lab and pilot scale. Clinical supplies or Investigational Medicinal Products (IMPs) are quality controlled and released by a Qualified Person. SEPS Pharma can also provide blinding and randomization of clinical materials.
GMP manufacturing capabilities include:
- Solutions
- Microsuspensions
- Nanosuspensions
- Spray drying
- Fluid bed granulation
- Bead layering
- Tablet manufacturing
- Capsules (encapsulation/over-encapsulation)