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PharmTech Europe
18 April 2017

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Top Stories

Nemera Joins European Project to Develop Inhaled Nanoparticles for Heart Disease

The project will foster the translation of nanomedicine applications for the treatment of cardiovascular diseases.
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Debate Over New Cancer Therapies

FDA is in the center of the debate over developing and pricing new cancer therapies.
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PAT for Continuous API Manufacturing Progresses

Advances in process analytical technology have been achieved, but significant challenges remain.
/ read more /

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Industry News

Researchers Study Vaccine Responses in Newborns

In a new study, researchers from Boston Children's Hospital study responses to pneumococcal vaccine in infant monkeys.
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ISPE Publishes Data Integrity Guide

The new guide offers guidance on how to ensure data and records are complete, consistent, secure, accurate, and available throughout their lifecycle.
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Regulatory News

EU–US Mutual Recognition Agreement on GMP Inspections

Both the European Union and United States are still ironing out issues such as confidentiality of information and recognition of competence of each party's regulatory authorities in their agreement on GMP inspections.
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EMA Updates Flu Vaccination Recommendations

The agency issued its recommendation for the influenza virus strains European vaccine manufacturers should include for 2017.
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More Regulatory News

Bio/Pharma News

Janssen Signs Deal with PeptiDream

Janssen will use PeptiDream's proprietary Peptide Discovery Platform System technology to identify peptides against multiple metabolic and cardiovascular targets.
/ read more /


Dipharma Strengthens Pipeline with Stable, Fast-Dissolving Carglumic Acid Tablets

Carglumic acid is used in the management of rare, life-threatening inborn metabolic disorders affecting the urea cycle.
/ read more /


More Bio/Pharma News

Supplier News

Colorcon Launches Colorcon Academy

This platform is designed to give pharmaceutical professionals a deeper knowledge of excipient functionality, core formulation, film coating, and controlled release of oral solid dosage forms, along with regulatory insights.
/ read more /

GE Healthcare: The Next Cell and Gene Therapy Manufacturing Giant?

GE Healthcare continues to ramp up its offerings in the bioprocessing space with the purchase of Asymptote and a continued partnership with Zenith Technologies.
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FEATURED TOPICS

FORMULATION

Developing Cannabis-Based Therapeutics

David Fulper, PhD, director of technology support at Catalent, shares insights on the challenges and opportunities for cannabis-based therapeutics.
/ read more /

 

OUTSOURCING

Staffing for China's Rapidly Growing Biomanufacturing Industry

New study shows China biopharma companies face staffing shortages.
/ read more /

QUALITY

Critical Quality Attributes Challenge Biologics Development

The complex nature of biologics adds additional CQAs that must be determined to ensure the safe development of biologics.
/ read more /

ANALYTICS

Morphologically-Directed Raman Spectroscopy: Uncovering the Good, the Bad, and the Ugly in Drug Formulations

MDRS differentiates the API from the product matrix and enables measurement of particle size and shape.
/ read more /


Product Profiles

ITW REAGENTS

pH Adjustment in Pharmaceutical Production
ITW Reagents is fully integrated by AppliChem GmbH and PanReac Química SLU companies, under unique commercial brand PanReac AppliChem since 2014. With 75 years' of experience, ITW Reagents is a Chemical producer of high quality chemicals for pharmaceutical manufacturing processes.
/ Read more/

PROCAPS / Softigel

Innovation with Softigel will be everywhere this May, come meet with us!
Softigel by Procaps offers Contract Manufacturing & Product Development services in advanced softgel technologies, focusing on difficult-to-produce compounds, unique formulations, innovative dosage forms, and non-traditional manufacturing processes.
/ Read more/

Shimadzu

Universal solution for automated HPLC method development
Shimadzu's Nexera Method Scouting system provides an outstanding platform for efficient HPLC method development and implementation. It is based on the Nexera X2 next-generation ultra-high performance liquid chromatograph, an all-round LC system for ultra-high-speed analysis.
/ Read more/


UP COMING WEBCAST

A Complete Guide to USP <232> & <233> Pharmaceutical Elemental Impurities – Understanding Pharmaceutical Elemental Impurity Regulations and Laboratory Considerations
Live Webcast: Thursday, April 20 at 11:00am EDT
Register now



A Complete Guide to USP <232> & <233> Pharmaceutical Elemental Impurities – Implementing Pharmaceutical Elemental Impurity Sample Preparation and Analysis
Live Webcast: Wednesday, May 10 at 11:00am EDT
Register now


Events

Making Pharmaceuticals

Coventry, United Kingdom

25–26 April 2017

Respiratory Drug Delivery (RDD) Europe 2017

Nice, France

25–28 April 2017

Interpack 2017

Dusseldorf, Germany

4–10 May 2017

OSD Continuous Manufacturing in the Current Regulatory Landscape

Floriana, Malta

8–9 May 2017

CPhI North Amercia

Philadelphia, United States

16–18 May 2017


more events

Reference Library

Pharmaceutical Technology presents its Process Analytical Technology resource guide combo

A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, be more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects.
/ Click here /


More Reference BookS

eBOOKS

Quality Throughout the Supply Chain

Quality issues can appear at any stage of the bio/pharmaceutical development and manufacturing supply chain. Drug companies must monitor raw materials, suppliers, contract service providers, facilities, manufacturing processes, and production workers. In this e-book, the editors examine current quality issues, and how the industry is addressing quality challenges throughout the supply chain.

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