Eurofins Ireland >> BioPharma Services

BioPharma Services


With 50 years of delivering comprehensive laboratory services, Eurofins  enables pharmaceutical and biopharmaceutical companies to advance candidates from development through commercialization while ensuring regulatory compliance, cost effectiveness, and achievement of timelines. For a seamless service experience, customers team with scientists and project managers throughout the outsourcing process from testing to monthly reports to 24-hour online data access at LabAccess.comSM. Harmonized laboratory services at U.S. and Ireland sites as well as award-winning Professional Scientific Services® at customers' sites further broaden global drug development services.


  • Spectrophotometry (CD, Bradford, A280, BCA)
  • Electrophoresis (CE, SDS-PAGE, 2D gels, Western blots, IEF)
  • Chromatography (AAA, peptide mapping, glycan profiling, SEC, CEX, RP-HPLC and UPLC)
  • Mass Spectrometry (Ion trap, LC/MS/MS, ESI-TOF, MALDI-TOF, Orbitrap)

Molecular & Cell Biology

  • Cell Banking and Storage
  • Cell Based Potency Assays (Cell proliferation, cAMP, reporter gene, cell surface receptor binding)
  • ELISA (HCP, Protein A, sandwich ELISA, competitive ELISA)
  • qPCR (rDNA, Viruses)
  • Genetic Stability (custom)


  • Viral Clearance (Infectivity assays, qPCR assays)
  • Viral Safety Testing (in-vitro, retrovirus, reverse transcriptase assays)


  • Sterility & Mycoplasma Testing
  • Endotoxin
  • Environmental Monitoring and Organism Identification
  • Particulates
  • Microbial Limits
  • Preservative Effectiveness
  • Water Testing

Pharmaceutical and Biopharmaceutical

  • Drug substance and drug product, clinical, registration, and commercial stability testing
  • Marketed product release testing
  • Stability storage and product retain programs
  • Raw material/excipient testing (USP/NF, EP, JP) and Melamine testing
  • Residual Impurity investigation and analysis
  • Comparator product testing and clinical ID/re-assay testing

Specialized Services

  • Method development, optimization, cGMP qualification and validation
  • Expedited raw material and excipient testing (USP/NF, EP)
  • Container testing on plastic and glass
  • Extractables/Leachables testing
  • Process/facilities validation - viral clearance, residual impurity testing, extractables & leachables, water testing, environmental monitoring, on-site sample collection
  • Consulting/protocol writing.

Three Service Models

  • Fee For Service- Eurofins Lancaster Laboratories' staff performs work on project-by-project basis.
  • Full Time Equivalent - Eurofins' staff, at US or Ireland site, fully dedicated to clients' project needs.
  • Professional Scientific Services®- Eurofins' staff, hired, trained and managed by Eurofins, at client's sites.

Markets Served

With harmonized laboratory services within our U.S. and Ireland locations, Eurofins Lancaster Laboratories serves a broad spectrum of companies in the pharmaceutical, biopharmaceutical, medical device, and animal health industries and has a proven track record of providing quality scientific solutions to the world's largest pharmaceutical/biopharmaceutical companies as well as hundreds of virtual companies and CMOs. 


With facilities in Lancaster, PA, Portage, MI and Dungarvan, County Waterford, Ireland, Eurofins' facilities offer cGMP-compliant laboratory services and operate under harmonized quality control programs and LIMS. 


Clogherane, Dungarvan, Co. Waterford, Ireland
ph: +353 (0)58-48300