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Contract Service Directory
SGS Life Sciences
Company Headquarters
75 Passaic Avenue
Fairfield, NJ 07004
United States
Company Description
SGS Life Sciences is a leading contract service organization offering high quality analytical development, biologics characterization and quality control testing for over 40 years. We utilize cutting-edge techniques/technolog ies and are staffed by knowledgeable and experienced personnel, providing services through the drug development lifecycle.
Contract Service Directory
- Accelerated Stability Studies
- Analytical Laboratory Services
- Analytical Methods Development
- Analytical Validation Studies
- Assay Development
- Biological Testing
- Biosimilars
- Chemical Analysis
- Chromatographic Analysis, LC/GC
- CMC (Chemistry, Manfacturing & Controls)
- Container Testing
- Contaminant Analysis
- Contract Research
- Dissolution Testing
- Efficacy Testing
- Endotoxin Testing & Removal
- Environmental Analysis
- Environmental Monitoring
- Extractables / Leachables Testing
- Forced Degradation Studies
- HPLC
- Lot Release Testing
- Mass Spectrometry
- Methods Development
- Methods Validation
- Microbiological Control Services
- Microbiological Testing
- Mycoplasma Testing
- Packaging, Design & Testing
- Particle Characterization
- Particle Size Analysis
- Photostability
- QA/QC
- Quality Control Testing
- R&D Services
- Raw Materials Analysis
- Stability Studies
- Stability, ICH
- Sterility Testing
- Storage
- Technology Transfer
- Thermogravimetric Analysis
- Toxicology Services & Analysis
- Trace Metal Analysis, ICP
- UV-VIS Spectrophotometer Analysis
- Validation, Services
- Water Testing: Chemical
- Water Testing: Microbiology
- Wet Chemical Analysis
- X-Ray Powder Diffraction
Contract Services Directory
More Content From SGS Life Sciences
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Stability Testing According to ICH Guidelines or Customer Specifications
...Services Released on 08.06.2013
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Quality Control Testing of Raw Materials, APIs, and Finished Products
...Services Released on 08.06.2013
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Clinical Trial Materials | Process Development | Validation
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Breaking News | Clinical Trials | CRO News | GMPs/GCPs
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Breaking News | Chemistry | Collaborations & Alliances | CRO News | Drug Discovery | Methods Development | Preclinical Outsourcing | Toxicology
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Breaking News
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Analytical Services | Bioanalytical Services | Bioassay Development | Breaking News | Chemistry | Extractables and Leachables | Laboratory Testing | Promotions & Moves | R&D | Toxicology | Validation
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Bioassay Development | Drug Development | Methods Development | Preclinical Outsourcing | Process Development | Toxicology
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Breaking News | Clinical Trials | CRO News | Drug Discovery | GMPs/GCPs | Methods Development
Apricus Sells CRO Subsidiary
Apricus Biosciences has sold its specialty CRO subsidiary, Bio-Quant, Inc., to BioTox Sciences07.06.11
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Breaking News | Promotions & Moves
ABC Labs Adds to CMC Team
Brad Benson, Ph.D., has joined the CMC Development Services team at ABC Laboratories.06.09.11
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Breaking News | Industry News
Ricerca Sells Bothell Site to Numira
Ricerca Biosciences has sold its Bothell (West), WA in vivo operation to Numira Biosciences, a CRO specializing in high-resolution imaging and analysis of small animal specimens.02.15.11
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Breaking News | Promotions & Moves
Advanced Clinical
Julie Heneghan has been appointed vice president of Advanced Clinical. Ms. Heneghan has more than 20 years of experience in the outsourcing and staffing solutions industry.09.02.10
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Clinical Trials | Drug Development | R&D
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Preclinical Outsourcing | Toxicology
Smart Sponsor Moves for 2010
Timely tips for successful outsourcing experiencesSteve Snyder 05.10.10
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Breaking News | Chemistry | Drug Development | Industry News
PPD Launches Vax/Bio Center of Excellence
PPD, Inc. is launching the Vaccines & Biologics Center of Excellence, a network of integrated lab services focused on vaccine and biologic drug development.03.24.10
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Breaking News | Drug Development | Promotions & Moves
Covance
Herman E. Scholtz, MD, has joined Covance as vice president and general manager of global clinical pharmacology services.12.10.09
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Clinical Trials | Validation
EDC Focus: Making the Right Investment in CTMS/EDC
How to evaluate the solutionsJoseph J. Valeri 11.06.09
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Drug Development | Preclinical Outsourcing | Toxicology
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Chemistry | Excipients | Risk Management
Understanding Excipient Interfaces
Regulatory drivers for testing to better predict attributesAndrew Parker, Ph.D. 11.06.08
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Breaking News | Promotions & Moves | Toxicology
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Analytical Services | Bioanalytical Services | Breaking News | Clinical Trials | Industry News
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Drug Development | Regulatory Affairs
Clinical Research Outsourcing
Moving from transactional to strategic partnership-based outsourcingKenneth Getz and Rachael Zuckerman 05.30.08
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Drug Development | Logistics | Preclinical Outsourcing | Toxicology
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Chemistry | Clinical Trials | Preclinical Outsourcing | Toxicology
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Chemistry | Drug Development | Logistics | Toxicology | Validation
Bioanalytical Outsourcing
What factors affect outsourcing decisions?Anthony J. DeStefano and Stephen Lowes 11.09.07
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Clinical Trials | Drug Development
Contracting Research: Criteria to Live By
How do we develop best practices for CRO partnerships?Jeffrey Steinberg and Karoline Dubiel 09.06.07
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Breaking News | Promotions & Moves
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Drug Development | Toxicology
Warning Signs?
Is there too much pressure in the preclinical drug development pipeline?Steve Snyder 04.02.07
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Drug Development | Preclinical Outsourcing | Toxicology
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Preclinical Outsourcing | Toxicology
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Breaking News | Clinical Trials | Industry News
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APIs | Chemistry | Drug Development | Drug Discovery | Inspections | Process Development | Supply Chain
Domestic Outsourcing for Drug Discovery
Guidelines for early-stage research issuesJeffrey M. Marra 09.13.06
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Breaking News | Drug Discovery | Industry News
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Chemistry | Clinical Trials | Drug Development | Drug Discovery
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Chemistry | Drug Development | Drug Discovery | Information Technology | Process Development | Process Validation | Risk Management | Validation
Industry Consolidation
Our year-end review of merger & acquisition activityMichael A. Martorelli 08.23.05
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Drug Development | Inspections | Validation
Sponsor Expectations for Stability Programs
Some guidelines for sponsor inspectionsMargaret B. Voelz 08.22.05
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Analytical Services | Bioanalytical Services | Clinical Trials | Drug Development | Drug Discovery
Outsourcing Drug Development
How to take advantage of a CROs experience and cultureDouglas J. Squires, Ph.D. 08.22.05
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Chemistry | Clinical Trials | Drug Development | Toxicology | Validation
Managing CRO Selection
How will the rise of specialist intermediary organizations affect the process?David Cavalla, MA 08.22.05
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Capsules | Drug Development | Extractables and Leachables | Facilities | Fill/Finish | Formulation Development | GMPs/GCPs | Lyophilization | Parenterals | Preclinical Outsourcing | Process Development | Process Validation | Scale-up/Technology Transfer | Solid Dosage/Semi-solids | Toxicology | Validation
Early Phase Outsourcing
A sponsor discusses the benefits of moving outsourcing earlier in the value chainAnthony De Stefano 08.22.05
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Analytical Services | Bioanalytical Services | Bioassay Development | Cleaning Validation | Drug Development | Drug Discovery | Methods Development | Preclinical Outsourcing | Process Development | Process Validation | QA/QC | Toxicology | Validation
Full-Time Equivalent Agreements
An alternative strategy for long-term outsourcing of cGMP services.Thomas Wilson, Magdalena R. Mejilano 08.22.05
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Clinical Trials | Drug Development
The CRO Industry: Opportunities and Trends
Global read, alliances and EDC continue to growKristin Brooks 06.21.05
