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PharmTech Europe

19 July 2016

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Top Stories

EAG Inc. Rebrands Businesses, Including ABC Labs, as EAG Laboratories

EAG Laboratories announces new company identity and intent to expand testing, analysis, and characterization capabilities across multiple markets.
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EMA Performs Risk Reviews on Several Medications

The agency reviews hemophilia A, skin, and diabetes treatments, among others.
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EXPERT INTERVIEW

Angelo Stracquatanio, co-founder of Apprentice Field Suite, spoke with Pharmaceutical Technology about smart glasses and their use in pharmaceutical manufacturing.

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Industry News

Researchers Present Novel Method for Scale-Up of Stem Cell Production

This new method uses inter-alpha inhibitors to promote attachment and long-term growth in stem cells.
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Are Oral Peptide Drugs on the Horizon?

A new study examines the oral delivery of protein drugs in plant cells and hypothesizes that the cold storage and transportation of biologics could someday be eliminated.
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Regulatory News

EMA Determines Benefits of Zydelig Outweigh Risks

The agency completes its risk assessment of the blood cancer treatments.
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Sandoz's Biosimilar to Enbrel Gets FDA Support Ahead of Panel

FDA reviewers have found that Sandoz's GP2015, a biosimilar version of Amgen's Enbrel, is highly similar to the original product in terms of purity, safety, and potency.
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Bio/Pharma News

Teligent Breaks Ground on Manufacturing and R&D Expansion

Teligent is expanding its manufacturing and R&D complex in New Jersey.
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Federal Court Weighs in on Biosimilar Patent Dance

A Federal Circuit court ruled biosimilar makers must wait 180 days after receiving FDA approval before bringing drugs to market.
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Bio/Pharma in China
New Initiatives, New Opportunities

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Supplier News

UPS Expands Capabilities for Drug and Vaccine Research

UPS will expand its clinical trial logistics capabilities to include drug and vaccine development.
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Alexion to Build Biologics Manufacturing Facility in Ireland

The company will invest €100 million in the expansion of its Athlone facility.
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FEATURED TOPICS

FORMULATION

Taking On Mission Insoluble with Polymers

Polymers have played a key role as solubilizing excipients. Industry experts explain why polymer structures and functionalities are important considerations in formulation development.
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DRUG DEVELOPMENT

The importance of lipid screening in the development of lipid-based formulations

Lipid-based drug delivery is increasingly being used to tackle oral bioavailability challenges resulting from poor solubility.
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PEER-REVIEWED RESEARCH

Evaluating Practical Uses of Molecular Isotopic Engineering

The authors' directed isotopic synthesis is one example of how molecular isotopic engineering can be used to predetermine the discrete isotopic ranges of biopharmaceutical products.
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MANUFACTURING

Data Integrity Challenges in Manufacturing

Designing systems using the principles of good documentation practice, including validated audit trails, is a key piece of a manufacturing data integrity program.
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Webcasts

Drug Stability Testing from Development to Shipping

On Demand

In this educational webcast, learn about regulatory expectations and practical approaches to stability testing of drug substances and drug products for clinical trials, packaging, storage, and transportation.
Sponsored by SGS Life Science Services


Engineering the Mechanical Properties of Amorphous Spray-Dried Dispersions

On Demand
Capsugel Dosage Form Solutions will present a webinar discussing the aspect of engineering spray-dried dispersion properties, with a particular emphasis on the impact of atomization and drying rate on powder mechanical properties.
Sponsored by Capsugel


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Events

14th Annual Pharmaceutical IT Congress

28-29 September, 2016 | London, England

CPhI Worldwide

4-6 October, 2016 | Barcelona, Spain

PDA Visual Inspection Forum

25-26 October, 2016 | Berlin, Germany


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Reference Book

Pharmaceutical Technology Drug Delivery Guides Pharmaceutical Technology Solid Dosage Combo

Increase your knowledge of solid dosage technology and solid dose tablet manufacturing processes. These comprehensive pharmacology reference guides cover a variety of solid-dosage form principles such as oral solid-dosage forms, powders, mixing and blending, excipients, tableting, and coating. Drug delivery system manufacturing professionals can use the solid dosage manufacturing books to stay current with compressed tablet manufacturing processes, solid dosage processing equipment, tablet-pressing processes, and pharmaceutical industry trends in oral solid dosage manufacturing and solid dosage form development.
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More Reference Book

eBOOKS

Bioprocessing & Sterile Manufacturing eBook

Read feature articles on accelerated scale-up for vaccine production, standards for air cleanliness classification, aseptic filling advances, a flexible approach to cleanroom design, a science-driven approach for microbial control, removing genotoxic impurities, regulatory enforcement, drug shortages, and validation of single-use shipping systems.

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