With Pace® Life Sciences, you have a partner who understands the unique requirements of your business and industry; one who can provide the technical expertise, innovation and world-class facilities that enable you to bring products to market faster and meet all the current quality, health and safety standards. For more than 30 years, Pace® has been advancing candidates from early pre-formulation and tox studies to an IND filing and on through the clinical phases. Our extensive GMP clinical supplies manufacturing capabilities include oral/solid/liquid and topicals capabilities, sterile fill-finish and clinical packaging and kitting for a variety of molecules/dosage forms.
Explore Our Services
Drug Discovery
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Preclinical Safety Studies
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Early Formulation Development
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Clinical Trials
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Technology Transfers
Characterization of Novel Molecules & Biologics
Text Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Manufacturing Process
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
CH Stability Programs
Raw Materials Clearance
Finished Product
Production Quality Monitoring
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Drug Discovery
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Preclinical Safety Studies
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Early Formulation Development
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Clinical Trials
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Technology Transfers
Characterization of Novel Molecules & Biologics
Text Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product
Manufacturing Process
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
CH Stability Programs
Raw Materials Clearance
Finished Product
Production Quality Monitoring
Characterization of Novel Molecules & Biologics
Test Article Preparation
Formula Development
Lyophilization/Spray Drying/Hot-melt Extrusion/Milling
Analytical Development
GMP Clinical Trial Manufacturing
Reference Standard Programs
Microbiology
Extractables - Leachables
ICH Stability Programs
Raw Materials Clearance
Finished Product