Services List
Consulting and laboratory services to the pharmaceutical and medical device industries.
With our integrated consulting, laboratory, and contract sterilization capabilities, we are uniquely organized to meet the requirements of the biologics, pharmaceutical and medical device industries. Services include, but are not limited to:
- Routine Product Release Testing: sterility, LAL, bioburden, cytotoxicity
- Routine Contract EO and Steam Sterilization Services: including cycle development and validation
- Validation of Gamma and E-beam Irradiation Sterilization Processes
- Validation Services: Process, Equipment, Method, Software, Cleaning, Laboratory
- Environmental Monitoring: viable, non-viable, bioburden
- Microbial Suspensions and Growth Promotion Organisms
- Quality System Consulting: compliance audits and customized training
- Custom R&D Projects: product performance evaluations, microbiology, product/process development, small volume contract packaging and manufacturing
- Biological Indicator Testing-EO, Steam, custom: Performance verifications, D-value, z-value, survivor/kill, custom production
- Training and Seminars
- Regulatory Assistance: 510(k) and PMA preparations, 483 preparations, 483 and warning letter responses
- Compliance Auditing: QRS, Laboratory, cGMP, and Computer Systems
- Dietary Supplements: Quality, Auditing, Assessment
- Health Care Facility Practice Support
- Packaging Solutions
Please feel free to download our company brochure:
Download BrochureIntegrated Services Overview
LexaMed is Global
LexaMed is internationally focused.
In addition to US-based projects, LexaMed also has a global client base with projects in:
Puerto Rico
India
China
The Netherlands
Germany
Singapore
Spain
Ireland
Denmark
Korea
Thailand
Malaysia
Brazil
Argentina
Canada
