Sterile Empty Vials: Made for purity in every last detail
Our staff is continually trained in all best practices and quality assurance to ensure expertise in creating sterile empty vials (SEVs) that meet your needs and standards.
EXPLORE OUR VIALS Order by phone
United States
800-325-7354Mon-Wed: 7:30 AM to 5:30 PM CST
Thu-Fri: 7:30 AM to 5:00 PM CST
Canada
800-663-0972Mon-Fri: 8:30 AM to 5:00 PM EDT
Order online
To order vials online, please visit MyALKUS.com to create a login and explore our Product Catalog.
Get samples
Our sample kit includes our full range of 13 types of empty, sterile clear and amber vials.
Full Product Catalog
DownloadAccess our full Product Catalog to view our large range of size and color options. Receive a Certificate of Analysis with your next order to verify that our products meet all regulatory requirements.
USP Standards Report
DownloadAll SEVs are manufactured with United States Pharmacopeia (USP) Type 1 borosilicate glass and meet USP <660> requirements. Download our USP Standards Report to learn more about our manufacturing standards.
Vials that meet our standards and yours
Rigorous control measures are employed to provide the quality and consistency of ALK Life Science Solutions™ vials at every step of the process — from the materials we use to the way each vial is assembled.
Assembled in a Class 100 cleanroom environment in the United States
All equipment undergoes regularly scheduled calibration, maintenance, validation, testing, measuring, and utilization procedures.
About our materials
Our vial stoppers are composed of a latex- and rubber-free chlorobutyl formulation.
SEVs are aseptically assembled in the United States using sterile components, including glass and stoppers, for final product sterility.
Some of our SEVs come equipped with FluroTec®—an extra barrier against extractables and leachables that minimizes the risk of impurities, interactions, and medicine degradation.
Integrity and quality are our top priority
We strictly adhere to the FDA's Current Good Manufacturing Practices (CGMPs) regulations, mitigating the potential for contamination that could impact the integrity of patients' therapies.
These regulations tightly govern design, monitoring, and control of manufacturing processes and facilities.
These regulations tightly govern design, monitoring, and control of manufacturing processes and facilities.
Our SEVs are all assembled, sterilized, and tested at our plant in the United States and adhere to USP requirements.
All SEVs are eligible to be sold internationally.
All SEVs are eligible to be sold internationally.