IntegrityBio

Aseptic Filling and Finish

Our filling capabilities include vials and syringes for both liquid and lyophilized presentations with a high accuracy for both aqueous and viscous solutions. Both manual and automated filling capabilities allow us to offer many different batch configurations and sizes.

Integrity Bio's aseptic filling and capping processes utilize industry proven equipment which provides the most efficient control of the production fill line. Our automated fill and stopper machine is capable of producing 2mL to 20 mL batches of either liquid or lyophilized runs all within a Class 100 environment.

Rolling diaphragm liquid filling pumps are utilized to provide Integrity Bio Inc. clients with the highest quality final product. Keeping the majority of the process disposable assures our clients the best possible solution to cleaning validation efforts and concerns.

Is this your Organization?   Request Access

Locations


United States
Integritybio
820 Calle Plano
Camarillo, CA  93012
United States, North America

Contacts


No Contacts Created Yet

Production Lines

Integritybio    Aseptic Fill and Finish
Location: Camarillo, CA, United States
Main Details
Specialization:  Drug Product (Fill/Finish)Drug Product (Fill/Finish)
Dosage Form:  LiquidLiquid
Batch Size:  1-5,0001-5,000
Supported Vial Size:  2 ml2 ml
Supported Vial Size:  3 ml3 ml
Supported Vial Size:  5 ml5 ml
Supported Vial Size:  10 ml10 ml
Supported Vial Size:  20 ml20 ml
GMP Level:  Phase I/IIPhase I/II
Biosafety Level:  Not SpecifiedNot Specified
Additional Services
Analytical Services are Not AvailableAnalytical Services
Formulation Development is Not AvailableFormulation Development
Preclinical Manufacturing is Not AvailablePreclinical Manufacturing
Stability Studies are Not AvailableStability Studies
Prefilled Syringes are Not AvailablePrefilled Syringes
Viral Manufacturing is Not AvailableViral Manufacturing
Availability: Contact CMO

Last Update: 18JUN14

Send Inquiry about this Production Line
Integritybio    Lyophilization Facility
Location: Camarillo, CA, United States
Main Details
Specialization:  Drug Product (Fill/Finish)Drug Product (Fill/Finish)
Dosage Form:  LyophilizedLyophilized
Batch Size:  1-5,0001-5,000
Supported Vial Size:  2 ml2 ml
Supported Vial Size:  3 ml3 ml
Supported Vial Size:  5 ml5 ml
Supported Vial Size:  10 ml10 ml
Supported Vial Size:  20 ml20 ml
GMP Level:  Phase I/IIPhase I/II
Biosafety Level:  Not SpecifiedNot Specified
Additional Services
Analytical Services are Not AvailableAnalytical Services
Formulation Development is Not AvailableFormulation Development
Preclinical Manufacturing is Not AvailablePreclinical Manufacturing
Stability Studies are Not AvailableStability Studies
Prefilled Syringes are Not AvailablePrefilled Syringes
Viral Manufacturing is Not AvailableViral Manufacturing
Availability: Contact CMO

Last Update: 18JUN14

Send Inquiry about this Production Line

Copyright © Kymanox, All Rights Reserved.