Our Promise To Our Partners - Experience, Enthusiasm and Expertise

As each partner is unique, we approach each project to fulfill their specific requirements and tailor our contract pharma services accordingly. Our manufacturing capacity gives your product the flexibility to grow and mature and is ideally suited, should it be required, to handle complex manufacturing requirements.

pharmaceutical contract manufacturing

Experience and expertise:

  • 45 years providing contract pharma services to our partners
  • Multiple products successfully tech transferred to commercial scale for our partners

Speed to market:

  • Proven efficiency with on-site scale-up and manufacturing services including registration support to provide a fast efficient service
  • Capacity to design, build, commission, qualify and commercialize solid oral dosage and powder/liquid fill-finish processes on-site

Compliant, reliable and cost efficient supplier:

  • Excellent compliance record in U.S. and Europe with experienced and motivated staff
  • Flexible infrastructure and efficient operations with mature and embedded Lean 6 Sigma/Operational Excellence programs
  • Consistently high customer satisfaction levels – established site metrics to track and measure performance (including OTIF and RFT)

Effectiveness of transfer:

  • We leverage through process and product understanding, honed risk assessment, process modeling and optimized experimental approaches to maximize transfer effectiveness
  • We employ Process Analytical Technology (PAT) as part of our on-going process improvement activities and will incorporate, where appropriate, these activities into your tech transfer
  • We work to ensure transferred processes are robust and thorough through process documentation, QA systems, calibration and maintenance activities that are targeted towards key process variables/steps (i.e. waste elimination and error proofing by design)

Dedicated customer service:

  • We believe in the importance of open communication
  • A dedicated project management resource will keep you informed at all stages in the project/commercial supply arrangement

Access to full capabilities of our sites:

  • Capacity of 2.5 billion solid dosage, 10 million vial and 2 million syringe units, process and analytical equipment, high potency product scale-up and manufacturing, DEA-controlled site, packaging facilities in U.S. and E.U.
  • Full CMC package capabilities for regulatory registrations

Opportunity to examine tax options:

  • Athlone, Ireland facility is located in a Low Tax Jurisdiction (LTJ)

For a list of our Partners, please click here