- Excipients are ISO9001 and ICH Q7 cGMP certified
- Manufacturing, purification, crystallization, blending, and finishing of high-purity chemicals to customized specifications
- Full supply chain traceability, global strategic sourcing, formalized qualification, full lot traceability, and supplier rating and audit program.
Supporting Scientific Advances for Human Health
With Avantor®, you have the power of world-class manufacturing and distribution for all your business needs – all in one place.
Aurora Manufacturing Facility
Briare Manufacturing Facility
- ISO9001, ISO14001, OHSAS18001
- Filling of high-purity solvents and corrosives
- Mixing capabilities: water-, solvent-, and corrosive-based
Chester Manufacturing Facility
- ISO 9001
- Propriety quality system designed to meet evolving needs of pharmaceutical and biotech customer
- Production of HPLC and other high-purity grades of acetonitrile and methanol for laboratory and biopharmaceutical applications
- Packaging of HPLC acetonitrile and methanol into bulk tankers and returnable containers
Dehradun Manufacturing Facility
- High quality diagnostic kit production
- ISO 13485 certified
Gliwice Manufacturing Facility
- ICH Q7 certification
- AQAP 2110 certified
- Solvents purification and packaging, high purity acids packaging, WFI solutions, and salts synthesis production
Haasrode Manufacturing Facility
- ISO9001, ISO14001, OHSAS18001
- cGMP certificate
- Filling of pharma-grade solvents and liquids, liquids in general, and solids in pharma and non-pharma grades
- Mixing capabilities: water-based, solvent-based, corrosive-based, and custom-made solutions
Mexico City Manufacturing Facility
- Manufacturing of salts, solvents, and acids including packaging capabilities
- High purity water generation and mixing capabilities
- ISO 9001-2015 certified
Panoli Manufacturing Facility
- ISO 9001-2015 certified
- cGMP high purity solvents purification with packaging capabilities
Paris Manufacturing Facility
- ICH Q7 certification, FDA registered
- ISO 9001-2015 certified
- cGMP excipient down packaging, cGMP acids and solvents packaging, cGMP WFI solutions, semiconductor grade blends
Phillipsburg Manufacturing Facility
- ICH Q7 certification
- FSSC 22000:2018 certified
- cGMP excipient salts production and down packaging, cGMP acids and solvents purification and packaging, cGMP solutions, semiconductor grade blends
Sidney Manufacturing Facility
- Propriety quality system designed specifically to meet industry standards
- Three ICP-MS units on site for trace metal analysis
- Ultra-pure acid and base manufacturing
- Research and development for high-purity acid and semiconductor thin film deposition
Solon Manufacturing Facility
- FDA Registered Facility for Contract Manufacturing of Medical Devices (21CFR820)
- ISO 13485; ISO 9001; ISO 17025 Accredited for select laboratory methods; EXCiPACT certified (for scope of products)
- Manufacturing and supply of high-purity biochemicals, reagents, and custom services for life sciences
St. Louis Manufacturing Facility
- FDA Registered; Compliant to ICH Q7, 21CFR 210-211, IPEC
- Manufacturing of Active Pharmaceutical Ingredients (APIs) and High-Purity Ingredients (HPIs) such as cGMP excipients and advanced intermediates
- Multi-step organic synthesis, chromatography and crystallization with robust product development
Singapore Manufacturing Facility
- ICH Q7 cGMP
- cGMP excipient down packing
Case Studies
Our manufacturing specialists develop custom solutions that enable improvements in manufacturing quality, capacity, and speed to market.