American Pharmaceutical News In Review

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December 16, 2019

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Improve the Efficiency of High Throughput Catalyst Screening

While organizations have invested in automation equipment to support high throughput (HT) experimentation, the variety of resulting software systems require error-prone manual data transfer. These systems also fail to connect results with the reaction array impacting your ability to make decisions quickly.

Katalyst D2D software provides a single interface for HT catalyst screening—from experiment planning, through execution, to data analysis. Automated assembly of analytical data with each well of an array ensures data integrity and fast, confident decision-making.

	Industry News

FDA Grants VistaGen Fast Track Designation for Social Anxiety Disorder Treatment
VistaGen announced the FDA has granted Fast Track designation for development of the Company's PH94B... read more »

EicOsis Announces First Subject Dosed in Pain Management Trial
EicOsis announced initiation of dosing for the first human subject in a Phase 1 trial of EC5026, the... read more »

GIOSTAR in Process of FDA Approval for Type 2 Diabetes Clinical Trial
GIOSTAR announced they are in the process of approval from the FDA to conduct type 2 diabetes ... read more »

NCCN, Pfizer Announces Funding for Metastatic Breast Cancer Projects
The NCCN Oncology Research Program announced the proposals that were selected to receive funding, in... read more »

OrthoGrid Systems Receives FDA 510(K) Clearance for PhantomMSK Trauma Application
OrthoGrid Systems announces its newest application, PhantomMSK Trauma, has received 510(K) clearance... read more »

Diasome Announces New Chairman of Scientific Advisory Board
Diasome Pharmaceuticals named Dr. Jeremy Pettus the chairman of the company’s scientific advisory ... read more »

	Featured Articles

A Summary of USP’s Workshop on “The Future of Endotoxins and Pyrogen Testing: Reference Standards and Procedures” All parenteral articles and medical devices that contact body tissue or fluids have to be sterile ... read more »

Drug Delivery Roundtable The drug development process involves rigorous in vitro and in vivo studies to understand ... read more »

	Featured Video

Watch Video: The Clean Facility of the Future - Advanced Microbiology Techniques for Cleaner Facilities and Purer Products
Learn about the tools, techniques, services and best practices being used to manufacture high quality products while minimizing contamination and ... read more »

On-Demand Webinar: Extractables and Leachables of Biopharmaceutical Container Closure Systems: A Case Study by Pace Life Sciences (PLS)
In this webinar, you'll learn results and analysis of an internal E&L case study of biopharmaceutical single use bag systems, an overview of the ... read more »

	Featured Products

AeroTrak+ Remote Airborne Particle Counters
read more »

i-Series Integrated HPLC Systems
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	Featured Whitepaper

Objectionable Microorganisms: Keeping Bad Bugs Out of Good Products
No pharmaceutical company wants to sell a non-sterile drug contaminated with objectionable microorganisms, but how does a company know which organisms are objectionable and how do they ensure their ... read more »

Neutralization Efficiency of ICR Swabs for Sanitized Surfaces in Aseptic Manufacturing Environments
Swabbing is a common method for environmental monitoring in aseptic filling lines for pharmaceuticals. The ICR Swab (Cat. No. 146529) is designed for a presence-absence test of microorganisms on dry, ... read more »

	Events

BIO Asia International Conference
Tokyo, Japan – 03/10/2020
BIO Asia International Conference is an exclusive partnering forum that brings together the global biotechnology and pharmaceutical industry with ... event details »

DCAT Week ‘20
New York, NY – 03/23/2020
DCAT Week is the premier business development event for companies engaged in pharmaceutical development and manufacturing and related industries. It ... event details »

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