Supporting you from pre-clinical to market with science-led expertise and unparalleled project delivery.
Collaborative and science-led
Our approach.
With extensive experience taking drug products from pre-clinical to early phase clinical studies and transitioning to scale-up whilst maintaining quality and regulatory compliance, our team of experts can support you with unparalleled project delivery and flexibility.
Oral, Nasal and Pulmonary Expertise
Accelerating your drug program with quality and confidence.
Across all stages of development our team support you in accelerating to the clinic, transitioning to Phase 2 and scaling up with quality and compliance.
Oral dosage forms
- Blending, dry granulation, milling, coating
- Tablets (IR, MR, SR, Minitabs)
- Capsules (API, Powder blend, lipid)
- Small molecules, biologics, NCEs
- Grams to 250Kg batch sizes
Nasal and Pulmonary dosage forms
- (Nasal) Powder and liquid dosage forms
- (Pulmonary) powder
- Spray drying intermediates, micronization, lipids
- Capsule filling, device filling
- Blister packaging
Pre-clinical
(Pre-clinical - Phase 1)
Supporting you with formulation development to accelerate to the clinic.
Early Phase
(Phase 1 - Phase 2)
Helping you transition from Phase 1 to Phase 2 with confidence.
Late Phase
(Phase 3 - Commercial)
Progress through late-stage with scale-up and commercial expertise.
Get in touch
If you’re looking to work with a CDMO that is flexible and nimble, then we’re here to help.
