YOU SEARCHED BY...
SEARCH BY...
Country
- Canada(1)
- France(1)
- Germany(2)
- India(1)
- Slovenia(1)
- Switzerland(1)
- United Kingdom(2)
- United States(24)
Contract Service Directory
Pace Analytical Life Sciences
Company Headquarters
1311 Helmo Avenue N.
Oakdale, MN 55128
United States
Company Description
Premier CDMO for early-phase drug development with sites in Boston and Philadelphia: preformulation, formulation development, analytical development, Test Articles, and Clinical Trial Materials. Comprehensive GMP laboratory services from sites in Minnesota and Puerto Rico: chemistry and microbiology support for commercialization and manufacturing.
Contract Service Directory
- Accelerated Stability Studies
- Analytical Laboratory Services
- Analytical Methods Development
- Analytical Validation Studies
- API Solubilization Technologies
- Assay Development
- Bioanalytical Analysis LC/MS/MS
- Biologics Process Development
- Blending
- Central Lab Services
- Chemical Analysis
- Chromatographic Analysis, LC/GC
- Chromatography
- Clinical Trials, Phase I
- Clinical Trials, Phase II
- CMC (Chemistry, Manfacturing & Controls)
- Container Testing
- Contract Development and Manufacturing Organization (CDMO)
- Contract Manufacturing
- Contract Packaging
- Contract Research
- Dissolution Testing
- Dosage Form Development
- Drug Development Services
- Environmental Monitoring
- Extractables / Leachables Testing
- Feasibility Studies
- Formulation Development
- Formulation Services
- Formulation, Controlled Release
- Gene Therapy & Testing Protocols
- Hot Melt Extrusion
- HPLC
- IND/NDA Submissions
- Lot Release Testing
- Lyophilization
- Manufacturing, Capsules
- Manufacturing, Controlled Substances
- Manufacturing, Creams & Ointments
- Manufacturing, Dose Form, Non-Sterile
- Manufacturing, Oral Drug Delivery
- Manufacturing, Orally Dispersible Tablet
- Manufacturing, Solid Dosage
- Manufacturing, Tablets
- Manufacturing, Topicals
- Mass Spectrometry
- Methods Development
- Methods Validation
- Microbiological Testing
- Packaging, Clinical Trial Materials
- Packaging, Clinical Trials
- Packaging, Creams & Ointments
- Packaging, Solid Dosage
- Parenterals Development
- Particle Size Analysis
- Photostability
- Physical Testing
- Process Development/Scale-Up Services
- QA/QC
- Quality Control Testing
- R&D Services
- Raw Materials Analysis
- RNAi Technology
- Spray Drying
- Stability Studies
- Stability, ICH
- Sterility Testing
- Technology Transfer
- Trace Metal Analysis, ICP
- UV-VIS Spectrophotometer Analysis
- Validation, Equipment Cleaning
- Validation, Manufacturing
- Water Testing: Chemical
- Water Testing: Microbiology
- Wet Chemical Analysis
- X-Ray Crystallography
- X-Ray Powder Diffraction
Contract Services Directory
Related Content
-
Bio News | Biosimilars
Know the Challenges of Biosimilar Manufacturing
Best Practices for a Competitive MarketJerry Martin, Pharmaceutical and Life Sciences Consultant to PMMI, and, Dr. Michiel Ultee, Principal, Ulteemit BioConsulting, LLC 04.11.18
-
Drug Development | Drug Discovery
AAPS Annual Meeting Preview
Sessions address Pharmaceutical Excipients, Emerging Partnership Models, Drug Delivery Strategies, and more11.01.17
-
Breaking News | Drug Delivery | Industry News | Inspections
Tapemark Passes Regulatory Hurdle
Manufacturing facility completes successful FDA pre-approval and general GMP inspection06.07.17
-
Inspections | Regulatory Affairs
-
Breaking News | Industry News | Inspections
-
Breaking News | Facilities | Industry News | Serialization
Optel Opens Site in Brazil
South America’s largest economy is in the process of implementing serialization legislation06.05.17
-
Breaking News | Facilities | Industry News | Inspections
-
Regulatory Affairs
The FDA and Metrics
The Agency and industry continue to work together to achieve FDA’s objectivesDavid Lonza, Lachman Consultant Services, Inc. 05.09.17
-
A Billion Reasons Why Innovation Works
How Pharma Tech Industries Turned A Complicated Effervescent Transfer Into A Manufacturing Milestone.
-
Bio News | Bioanalytical Services | Breaking News | Facilities | Industry News
Eurofins Expands Biopharma Testing Operations
New £4 million UK facility to house biopharmaceutical testing business04.06.17
-
Trump Picks New FDA Commish
Combatting high drug prices and overregulation likely to be high on agendaTim Wright, Editor 04.03.17
-
Breaking News | Industry News | Lyophilization
-
Breaking News | Industry News
Avista Pharma Spends $4mn to Upgrade Capabilities
Expands microbiology, sterility testing and microbial ID capabilities at Agawam facility03.27.17
-
Capsules | Solid Dosage/Semi-solids
Generic Drug Trends
Industry faces tighter capacity, consolidation, and drug pricing uncertaintyEdward S. Price, President, PCI 03.07.17
-
Regulatory Affairs
Challenges and Advantages of International Regulatory Inspections
A look at the processes and approaches followed by FDADaniel Barreto, Lachman Consultants 03.07.17
-
Aseptic Processing | Bio News | Breaking News | Facilities | Fill/Finish | Industry News | Inspections | Lyophilization
LSNE Completes Two FDA Inspections
FDA PAI and general GMP inspection of two aseptic manufacturing plants and QC laboratory completed successfully03.06.17
-
Clinical Trials | CRO News | Drug Development
-
Analytical Services | Laboratory Testing
Analytical Testing Outsourcing Trends Update
Spurred by many factors, global analytical testing services market is experiencing rapid growth in the range of 11% per year01.26.17
-
QA/QC | Regulatory Affairs
FDA’s Quality Agreements Guidance
Evaluation of FDA’s recently issued Contract Manufacturing Arrangements for Drugs: Quality Agreements Guidance for IndustryPaul Mason, Ph.D., Director of Lachman Consultant Services, Inc. 01.26.17
-
Analytical Services | Chemistry | Fill/Finish | Industry News
Whitehouse Labs, AMRI Increase E&L Expertise
Adds staff and critical instrumentation to the E&L group01.18.17
