American Pharmaceutical News In Review

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May 21, 2018

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Getting Your UV-Visible Spectrophotometer Ready for USP Compliance

LambdaTM 365 UV spectrophotometers are conceptualized to be in accordance with USP guidelines. Known for its high versatility and stability, low stray light and extremely high signal to noise ratio, Lambda 365 is a tailor-made solution to give you a seamless performance for USP guidelines.

	Industry News

FDA to Focus on Generics Delaying Tactics

Lilly to Acquire AurKa Pharma

Aerie Submits NDA to for Roclatan

FDA Approves Novel Preventive Treatment for Migraine

FDA Approves First Non-Opioid Treatment for Management of Opioid Withdrawal Symptoms in Adults

Crysvita Study Met Primary Endpoint

	Featured Articles

Pharmaceutical P.I.N. Points Patent Innovation News Pharmaceutical P.I.N. Points Patent Innovation News The purpose of this column is to highlight and summarize recent key patents in the pharmaceutical ... read more »

Limitations of Microbial Environmental Monitoring Methods in Cleanrooms Limitations of Microbial Environmental Monitoring Methods in Cleanrooms Regulatory agencies like the FDA and EMA requires pharmaceutical manufacturing companies to have an ... read more »

	Featured Video

Watch Video: Mobius® MyWay
Watch Video: Mobius® MyWay
The Mobius® MyWay Portfolio offers single-use that’s ready when you are. Choose from Stock, Select, or Choice to have the assembly you want when you ... read more »

On-Demand Webinar: Moving to Lean Lab: Integrating TOC, Conductivity, and Data Integrity
On-Demand Webinar: Moving to Lean Lab: Integrating TOC, Conductivity, and Data Integrity
Sievers M9 TOC Analyzers are designed to help increase efficiency in pharmaceutical manufacturing while complying with data integrity guidance. Learn ... read more »

	Featured Products

Biopharm UNIFI System
read more »

Universal Mycoplasma Detection Kit
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	Featured Whitepaper

HiCel SMCC
HiCel SMCC
The properties of microcrystalline cellulose have been tried to improve by co-processing MCC with colloidal silicon dioxide. read more »

The Race to Phase III: A Cautionary Tale of Scalability
The Race to Phase III: A Cautionary Tale of Scalability
As drug products move from preclinical through Phase IV development stages, clinical material demand grows tremendously. Production scale-up is rarely straightforward. Scaling up drug product ... read more »

	Events

Using Raman Spectroscopy for Quality Control of Packaged Raw Materials
Online – 05/23/2018
Raman is the most practical technique for raw material identity (ID) verification but it often requires a sampling step, which limits its ease and ... event details »

T3: Trials, Tech and Transformation
Raleigh, NC – 05/30/2018
T3 is back for 2018, bringing you the latest updates and top tips from across the clinical trials landscape. Connecting leading experts, influencers ... event details »

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