Therapeutics from bench to clinic begins with us - your local CDMO
Research and Development
DNA Sequence Analysis, Cloning and Transfection
Pool Selection, Cloning and Selection of Top Clones
Creation of RCB and Biosafety Testing
Cell Line Stability Studies
Bioreactor Clone Screening
Scale-up and Upstream / Downstream Process Development
Analytical Method Development and Qualification
Early and Late Stage Formulation Development
cGMP mAbs Manufacturing
MCB and WCB Cell Banking and Testing
50L, 200L or 500L SUB Production Bioreactors
AKTA Purification Platform
Viral Inactivation and Viral Filtration
Ultrafiltration and Diafiltration, Formulation
Bulk Drug Substance Storage
In-Process and Release Analytical Testing
Media and Buffer Manufacturing
Raw Material Testing
1L to 3000L Media and Buffer Manufacturing
Cold Storage Available
QC Analytical Testing
Clinical Drug Product (DP) Logistics
Clinical Label Design, Printing, Application, and Label Inspection
DP Packaging
Monitored and Regulated DP Storage
Qualified Worldwide DP Distribution
cGMP Training and Audit Preparation
Basic cGMP Best Practices
Cleanroom Gowning Training
Cell Culture Expansion Training
Aseptic Processing Training
Single-Use Bioreactor Training
Purification, Viral Inactivation, Viral Filtration, UFDF Training
FDA Audit Preparation
Antibody Discovery Services
Hybridoma Technology
Single B-Cell Technology
Display Libraries
Liability Engineering
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