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Global Pharmaceutical Services

View our comprehensive test services for pharmaceutical products.

Service CategoriesDrug PhaseLab Sites
Analytical Research & Development (ARD)
Method Development/Validation (MD/MV)

• Assay & Related
• Elemental Impurities
• Residual Solvents
• Extractables & Leachables
• Identification of Impurities and Degradation Products
• Investigations
• Consulting for CMC, Reg. Affairs & Product Approval (RCA)
Initial Product Qualification
Product Validation
Clinical Studies
pIND to Life Cycle
Management (LCM)
North America
Itasca, IL

Europe
Leuven, BE
Raw Material Testing (RMT)
• Compendial Testing (USP/EP/JP) for Excipients
• Method Feasibility and Verification
• Container/Closure Testing, USP <381>,<660>,<661>
Initial Product Qualification
Product Validation
Clinical Studies
QC Lot Release (Routine)
North America
Itasca, IL
SLC, UT

Europe
Leuven, BE
Stability Studies
• API Stability
• Drug Product Stability
• In-Use Stability Studies
• ICH Stability Storage at SLC
25C/60%RH, 30C/65%RH, 40C/75%RH and 2-8C
• Photostability at Itasca
API and Drug Product
Shelf-Life studies
North America
Itasca, IL
SLC, UT

Europe
Leuven, BE
Batch Release
• API Release
• Drug Product Release
QC Lot Release
(Routine)
North America
Itasca, IL
SLC, UT

Europe
Leuven, BE
Wiesbaden, DE
Microbial Testing + Sterility Assurance
• Bacterial Endotoxins (LAL) Test
• Bioburden
• Microbial Identification
• Environmental Monitoring (EM)
• Container Closure Integrity Testing (CCIT)
QC Lot Release
(Routine & Stability)
North America
Itasca, IL
SLC, UT

Europe
Leuven, BE
Wiesbaden, DE
Sterility Assurance – USP/EP
Closed Membrane Filtration

• Parenteral Drug
• Ophthalmic (eye drops, gels, ointments)
• Pre-filled syringes & devices
• Other pharma products
Initial Product Qualification
Product Validation
Clinical Studies
QC Lot Release (Routine)
North America
Itasca, IL
SLC, UT

Europe
Wiesbaden, DE*
Sterility Assurance – USP/EP
Direct Immersion

• Combination drug/device products
• Tissues & tissue-based products
• Medical devices
Initial Product Qualification
Product Validation
Clinical Studies
QC Lot Release (Routine)
North America
Itasca, IL
SLC, UT

Europe
Wiesbaden, DE*
*Wiesbaden offers sterility assurance services in traditional cleanroom suites.