Product Showcase

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TruBio DV Bioprocess Control Software
TruBio® DV software is a hardware independent, highly configurable interface to the DeltaV control platform that has been developed with GAMP4 methods and validated for cGMP applications.
RAMBIO® - Advanced Mixing Technology Revolutionizes The Capabilities Of Shake Flask Cultures
The RAMBIO® uses ResonantAcoustic® Mixing (RAM) technology to mix and aerate microbial cultures. When combined with the Oxy-Pump® stopper, which actively pumps air in and out of the shake flask, oxygen transfer rates up to 6-fold higher than orbital-shaken cultures can readily be achieved.
Sample Tracking Software
The TrackWise by Sparta Systems Sample Tracking solution ensures securely documented chain of custody information, by tracking samples from initial check-in through disposal or long term storage.
Batch Record Review/Release Software Solutions
TrackWise Batch Record delivers the flexibility to support batch record review and release functionality in a number of different business models.
Out Of Spec/Out Of Trend (OOS/OOT) Software Solutions
TrackWise by Sparta Systems solution for Out of Spec/Out of Trend (OOS/OOT) ensures potential product non-conformances are properly and efficiently investigated and handled through the tracking and managing of the initial report, phased investigation, root cause analysis and any resulting Corrective Action and Preventative Actions (CAPAs) and change controls.
Deviations Management Software
The TrackWise by Sparta Systems Deviations Management solution allows a broad range of deviations to be tracked and managed from initial inception, through investigation, root cause analysis through to the execution of corrective and preventative actions (CAPAs) and subsequent change controls.
Software Solutions For Product Recalls / Withdrawals
The TrackWise Product Recall/Product Withdraw solution improves response time to potential recalls by automatically tracking and managing the decision process to recall products from the initial recall request submission through the evaluation and resulting recall decision.
Pharmaceutical Inserts And Outserts
Pharmaceutical Inserts And Outserts
Catalent Pharma Solutions
Pharmaceutical Inserts & Outserts - Recognized as the leading manufacturer of pharmaceutical inserts and outserts, we have multiple full-service, world-class facilities. We have the capacity to produce over 100 million inserts per month.
Custom Folding Cartons
Custom Folding Cartons
Catalent Pharma Solutions
Custom Folding Cartons - We are the leading producer of pharmaceutical and consumer healthcare cartons with the production capacity to produce 150 million cartons per month.
RFID And Barcoding Services
RFID And Barcoding Services
Catalent Pharma Solutions
Catalent has the capability to manufacture RFID enabled labels for pharmaceutical manufacturers as well as the capability to tag and encode products with item specific data at our major packaging facilities.
Pharmaceutical Labels
Pharmaceutical Labels
Catalent Pharma Solutions
Pharmaceutical Labels- Our pressure-sensitive label production facilities are dedicated to the pharmaceutical industry with product manufactured in strict adherence to prescription pharmaceutical labeling controls.
Product Launch Services
Product Launch Services
Catalent Pharma Solutions
Our reputation is that we provide the fastest turnaround time for delivery of package inserts for new product launches in the pharmaceutical industry—typically within 24 hours of FDA approval—and in some situations only an 8-hour turnaround.
Drug Development Services: Preclinical Spectroelectrochemical Cell
Spectroelectrochemistry couples the ability of an electrochemical experiment to change the oxidation state of a solution species with the structural and quantitative capabilities of spectroscopy.
Non-GLP Services
BASi uses our own Culex® Automated In Vivo Sampling System to carry out a variety of non-GLP research functions.
Toxicology Services
BASi provides clients with fast, reliable, preclinical in-life and pathological data in compliance with federal guidelines.

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