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PharmTech Europe

16 February 2016

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Top Stories

Pfizer Announces Organizational Changes for Pending Allergan Merger

Pfizer names executive leadership team for combined organization upon close of proposed Allergan transaction.
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Europe Implements Measures to Prevent Falsified Medicines

The agency prepares a plan to implement new packaging safety features.
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Industry News

Danish Companies and University Collaborate on MRSA Vaccine

Barvarian Nordic, Evaxion Biotech, and the Technical University of Denmark announced plans to collaborate on the development of a vaccine for MRSA.
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Metrohm USA Announces 2016 Young Chemist Award Winner

Metrohm USA awards the 2016 Young Chemist Award to PhD candidate developing wearable sensors that can non-invasively monitor physiologically relevant chemicals.
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Regulatory News

FDA Publishes Blog On Modernizing Generic Drug Review Processes

Stephen Ostroff published a blog on FDA regarding goals to modernize the generic drug review process in an effort to increase patient access to generics.
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Celltrion’s Biosimilar to Remicade Likely to be Approved for All Indications

There are no clinically meaningful differences between Celltrion’s CT-P13 and Remicade, according to an FDA briefing released ahead of the formal panel meeting.
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Bio/Pharma News

Immunomedics Receives Breakthrough Therapy Designation for Breast Cancer Antibody-Drug Conjugate

FDA granted Immunomedics breakthrough therapy designation for the company’s investigational antibody drug conjugate for treatment of triple negative breast cancer.
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Vaccines Prove Effective and Cost-Effective

Vaccine R&D has grown exponentially in recent years, spurred by ethical and medical needs to combat lethal infectious outbreaks and increased funding from public and private agencies and organizations.
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Supplier News

MPI Reasearch Invests in Upgrades and Department Expansions

MPI Research plans to renovate more than 55,000 square feet of facility space as part of the company’s plan to invest in upgrades and department expansion.
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Pharmapack Europe Announces Award Winners

Innovations awarded at Pharmapack Europe include improvements for patient compliance and protection from errors, tampering, or misuse.
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FEATURED TOPICS

OUTSOURCING

Macro Matters

Heightened global uncertainty could slow bio/pharma development activity.
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FORMULATION

Assessing Antibody-Dependent Cell-Mediated Cytotoxicity

The reporter bioassay, used to evaluate ADCC activity of therapeutic antibodies, complements the classical ADCC assay.
/ read more /

API SYNTHESIS AND MANUFACTURING

Faster, Cheaper, and Greener

Hazardous reagents can simplify processes and provide higher yields and purities.
/ read more /

SUPPLY CHAIN

Cold Chain: Going the Extra Mile

Real-time GPS technology, better IT connections, and more conservative, controlled shipping temperatures are improving the shipment of sensitive pharmaceuticals.
/ read more /


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Next Generation HPMC Capsules
Bioequivalence and Functional Performance

On Demand
New in-vivo data demonstrating the performance characteristics of the next generation of HPMC capsules.
Read more



Product/Service Profile

L.B. Bohle Maschinen + Verfahren GmbH

Bohle dry granulator BRC
L.B. Bohle rounds off the comprehensive offer of granulation solutions with the dry granulator series BRC 25 and BRC 100. In the dry granulator powders are processed into fluid granules.
/ Read more /


Event Profile

7th Annual Global Drug Delivery & Formulation Summit
Date: 23 – 25 May 2016
Venue: Maritim proArte Hotel, Friedrichstrasse 151, Berlin, 10117, Germany
Discover delivery innovation with powerful partnership potential. You’ll hear the latest success stories, case studies and breakthrough within biologics and molecules.
Website: www.ddfevent.com
/ Registration /


Webcasts

Best Practices for Effective Product Transfer

On Demand

Considerations for preparing for the process transfer, ensuring equipment and materials consistency, and post-transfer activities will be discussed.
Sponsored by Rottendorf Pharma


Calibration and Qualification of Laboratory Instruments in Accordance with GMP Requirements

On Demand
Calibration, qualification, and the right appropriate level of routine testing for laboratory instruments are critical to ensuring high-quality results and maintaining GMP and USP compliance. Understand the relationship between these factors to optimize testing and be prepared for audit.
Sponsored by Mettler Toledo


more webcasts

on pharmtech tv

PharmTech TV

Addressing Pharma Industry Issues

Tablet Coating

Biologics Development and Manufacturing Trends

Events

BIO Europe Spring 2016

4-6 April, 2016 | Stockholm, Sweden

INTERPHEX 2016

April 26-28, 2016 | New York, NY

Global Drug Delivery and Formulation Summit

23-25 May, 2016 | Berlin, Germany


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 Library

eBOOKS

Bioprocessing and Sterile Manufacturing 2015 eBook

This eBook features articles on sterility testing, disposable technologies, parenterals, facility planning, mAb formulation, and more.

more ebooks
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