COMPANY DESCRIPTION
Recognized as the world’s leading testing, inspection and certification company SGS provides best-in-class contract development, testing and manufacturing services to successfully deliver high quality, safe and effective medicines to market.
As a leading contract service organization for over 40 years, we support clients from discovery to clinical development and commercialization, through research, product development, quality control testing, and manufacturing.
We provide a diverse range of trusted solutions that match our clients’ biologics and small molecule development needs, helping them navigate the complex worldwide regulatory requirements throughout the journey to market
FACILITIES
With 27 facilities in 11 countries, SGS Health Science ensures product and patient safety, as well as compliance with global regulations from any of our global facilities, including six conveniently located, GMP-certified facilities in North America:
US
• Fairfield, NJ
• Hudson, NH
• Lincolnshire, IL
• West Chester, PA
Canada
• Markham, ON
• Mississauga, ON
PRODUCTS, SERVICES & CAPABILITIES
Our scientific experts accelerate drug development using innovative techniques to provide better, safer treatments to patients through a consultative approach to development, formulation, GMP testing and clinical manufacturing.
GMP Testing
SGS offers a comprehensive scope of expert-led quality control testing for raw materials, APIs, and finished products to support product characterization, method development and validation, bioanalysis and final GMP product release through our technical expertise in:
• Chemistry
• Biochemistry
• Microbiology
• Molecular & Cell Biology
• Virology
Formulation & Development
We use risk mitigation strategies to identify the best-suited formulation for a given drug product and carefully examine properties of the drug substance to identify ways to overcome formulation challenges that arise.
Clinical Manufacturing
SGS can support fast First In Human (FIH), microdosing and formulated Phase 1 to Phase 3 clinical manufacturing for a variety of dosage forms, including traditional solid dose capabilities and oral liquids/ suspensions. We also support the clinical process through packing, labeling, randomization, and blinding and are able to distribute globally with relevant QP services..