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Analytical + Environmental
Air
Ambient Air
Indoor Air Quality
Meteorological Monitoring
Fenceline Monitoring
Stack/Source Emissions
Gas Phase FTIR Service
Vapor Intrusion/Soil Gas
Biota
Solids
Asbestos
Bedrock Sampling
Biosolids
Petroleum – Solids
Soil/Sediment
Solid Waste
Water and Liquid
Bioassay
Drinking Water
Lead and Copper
Groundwater
Petroleum – Water & Liquid
Surface Water
Wastewater/Stormwater
Waterborne Pathogens
Microbiology
Testing Services:
Air Vapor Intrusion
Asbestos Testing Services
1,4-Dioxane (Water)
Carbonyls / Aldehydes
COVID-19 / SARS-COV-2
Dioxin Furans
Dissolved Gases
Explosives / Chemical Warfare
Herbicides
Industrial Hygiene
Inorganic
Legionella/Waterborne Pathogens
Low-Level Mercury Analysis
Metals / Trace Metals
PAHS
PBDE(s)
PCBs
Pesticides
PFAS
Radiochemistry
Semi-volatiles
TCLP
Total Organic Halogens (TOX)
Total Petroleum Hydrocarbons
USP 797
VOCs
Whole Effluent Toxicity Testing
Special Projects:
Emergency / Disaster
Regulatory Support
Monitoring
Property Transfer
Remediation
Safe Drinking Water
Site Assessments
Waste Characterization
Life Sciences
CDMO/CRO Services
Small Molecules
Preformulation
Physicochemical Characterization
Solid State, Polymorph & Salt Screening
Compatibility Studies
Preclinical Support
Dosing Vehicles
Test Articles
Custom Bioanalytical
Method Development
Non-GLP Bioanalysis
Release and Stability Testing
Analytical Development
Method Development
Method Validation
Release and Stability Testing
Formulation Development
Developability Assessments
Injectables
Lyophilization
Ophthalmics
Tablets and Capsules
Solutions and Suspensions
Gels, Creams and Ointments
Specialty Technologies
Hot Melt Extrusion
Spray Drying
Nanomilling
Liquid Filled Capsules
Long-Acting Injectables
Clinical Supplies Manufacturing
Aseptic Fill Injectables
Ophthalmics
Tablets and Capsules
Solutions and Suspensions
Gels, Creams and Ointments
Clinical Packaging
Primary and Secondary Packaging
Labeling and Kitting
Biologics
Characterization
Purity and Identity
Post Translational Modifications
Aggregation and Structural Assessments
Parenteral Quality Attributes
Preclinical Support
Test Article Prep
Dosing Vehicle Formulation
Custom Bioanalytical
Method Development
Non-GLP bioanalysis
Release and Stability Testing
Analytical Development
Formulation Development
Developability Assessments
Preformulation Screening
Liquid Formulation Development
Ophthalmics
Lyo Formulation Development
Clinical and Material Compatibility
Long-Acting Injectables
Process Development
Solubility Enhancement
Spray Drying
Stability Enhancement
Purification-UF/DF
Enteric Protection
Clinical Supplies Manufacturing
Aseptic Fill
Long-Acting Injectables
Ophthalmics
Solids and Semi-Solids
Liquids and Suspensions
Inhalation/Nasal
Clinical Packaging
Primary and secondary packaging
Labeling and Kitting
Nucleic Acids
Characterization
Biophysical
Physiochemical
Preclinical Support
Test Article Prep
Dosing Vehicle Formulation
Custom Bioanalytical
Method Development
Non-GLP Bioanalysis
Release and Stability Testing
Analytical Development
Formulation Development
Sterile Acqueous
Lipid Nanoparticles
Other Nanoparticles
Process Development
Solubility Enhancement
Stability Enhancement
Clinical Supplies Manufacturing
Aseptic Fill
Clinical Packaging
Primary and Secondary Packaging
Labeling and Kitting
Novel Molecules
Characterization
Biophysical
Physicochemical
Preclinical Support
Test Article Prep
Dosing Vehicle Formulation
Custom Bioanalytical
Method Development
Non-GLP Bioanalysis
Release and Stability Testing
Custom Research and Development
Virus Like Particles
Viral Vectors
AAV
Nanoparticles
ADC
Central Laboratory Services
Raw Materials/Starting Materials
Drug Substance/API
Excipients/Intermediates
Compendial Methods
Custom Methods
Drug Products
Small Molecules
Biologics
Nucleic Acids
QC Batch Release
Cleaning Verification
ICH Stability
Storage Chambers
Freeze-thaw Cycling
Photodegradation
Reference Standards
Characterization
Storage and Distribution
Extractables/Leachables
Pharmaceutical Packaging
Implantable Polymers
Elemental Impurities
Physical-Functional
Container Closure Integrity
Viscosity – Syringeability
Tensile-Elasticity
Custom Methods
Microbiology
MLT – Bioburden
Antimicrobial Effectiveness
Sterility
Bacterial Endotoxins
Sub-Visible Particulates
Biological Indicator
Facility Qualification
Microbial Identification
Analytical Methods
Drug Substance/API
Impurities
Characterization Methods
Quantitative Assays
Qualitative Limit Tests
Activity Assays
Cleaning Verification
Method Tech Transfer
Method Life Cycle Management
Medical Device
Drug-Device Combination
Physical-Functional
Biological Risk Analysis
Extractables/Leachables
Polymer Molecular Weight
Surface Cleanliness
Particulate Counts
Elemental Impurities
Medical Device Microbiology
Microbial Bioburden
Sterility Testing
Bacterial Endotoxins
Biological Indicators
Microbial Identification
Facility Validation
Environmental Monitoring
EO/ECH Residuals
Professional Services
Regulatory and Compliance
Hazard Communication
Product Stewardship
Material Data Management
FDA Regulatory Consulting
Compliance and Audit Services
Scientific Staff
Laboratory Staffing
Customized Solutions
Performance and Management
Instruments
Maintenance and Repair
Calibration and Mapping
Facilities
Cleanroom Testing and Certification
Validation and Compliance
Laboratory Relocation
Environmental Monitoring
Industries
Agriculture
Consumer Goods
Education
Engineering and Construction
Environmental Consulting
Energy
Government
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Manufacturing
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Mining
Resources
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Menu
Industries
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About Pace
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Meet our Experts
History and Growth
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Resources
Case Studies
Case Studies
Air Quality MGP Remediation Case Study
Biota Fox River Case Study
Dioxin Furan Maine DEP Case Study
Hull & Associates Case Study
Radiochemistry Pfohl Bros Case Study
