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Tuesday, May 21, 2013
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Cytheris Announces CYT107 Orphan Designation in Europe for the Treatment of PML
Wednesday, July 11, 2012
Scientific advice also received from EMA on proposed PML pivotal study protocol.

PharmaNet/i3 Introduces PharmaNet/i3 Strategic Resourcing
Tuesday, June 26, 2012
Unified staffing and FSP provider designed to deliver tailored solutions.

PharmaNet/i3 Expands Configurable Randomization and Trial Supply Management Solution Offering
Friday, June 22, 2012
Custom IRT solutions deliver optimal study operating efficiencies and logistics.

Vetter Expands its Capacities and Services for Prefilled Syringes
Tuesday, June 19, 2012
The CDMO has enlarged its portfolio from early stage through commercial manufacturing.

Thermo Scientific Adds Large Molecule Functionality to its Industry-Leading LIMS for Bioanalytical Laboratories
Friday, June 08, 2012
Watson LIMS offers enhanced functionality for large molecule bioanalysis in pharmaceutical and CRO laboratories.

Glycotope Moves FSH-GEX™ into Phase-II Clinical Development
Friday, June 08, 2012
Company successfully complete Phase I studies of FSH-GEX™.

Fast Plasma Sample Cleanup with New Phree™ Phospholipid Removal Plates
Tuesday, May 22, 2012
Phenomenex Inc. introduces Phree Phospholipid Removal Plates for fast cleanup of plasma samples in pharmaceutical and clinical research laboratories.

AB SCIEX Expands Its iChemistry™ Solutions Portfolio With Sensitivity-enhancing Reagents for Mass Spectrometry
Tuesday, May 22, 2012
Amplifex™ Reagents support the company’s strategy to push the limits of detection.

Vetter Boosts Quality and Logistic Processes
Monday, May 14, 2012
Leading CDMO completes its brand new center for visual inspection and logistics.

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Showing Results 21 - 30 of 225
Scientific News
Dutch Public-Private Partnership Invests 28 Million Euro on Research into Personalized Medicine
The Netherlands' three Top Institutes for life-science research announce a joint research target to bring personalized medicine closer to reality.
FDA Grants Orphan Drug Status for Quark's QPI-1002 for the Prophylaxis of DGF in Kidney Transplant Patients
Company completes enrollment and dosing in the dose-escalation safety portion of a Phase 1/2 study.
Oncolytics Biotech® Receives MHRA Approval to Conduct Phase 3 Trial for REOLYSIN®
Conducting the trials in U.S. and Europe will allow Company to access the physicians that have worked with REOLYSIN in head and neck cancers.
Shenogen and Chemizon Announce Drug Discovery Collaboration Focused on Oncology and Endocrine Disorders
The agreement will create small molecule therapeutics targeting modulators of the ER-alpha 36 receptor.
Dutch Public-Private Partnership Invests 28 Million Euro on Research into Personalized Medicine
The Netherlands' three Top Institutes for life-science research announce a joint research target to bring personalized medicine closer to reality.
FDA Grants Orphan Drug Status for Quark's QPI-1002 for the Prophylaxis of DGF in Kidney Transplant Patients
Company completes enrollment and dosing in the dose-escalation safety portion of a Phase 1/2 study.
Oncolytics Biotech® Receives MHRA Approval to Conduct Phase 3 Trial for REOLYSIN®
Conducting the trials in U.S. and Europe will allow Company to access the physicians that have worked with REOLYSIN in head and neck cancers.
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