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PharmTech Europe
3 October 2017

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Top Stories

Global Effort to Stop Sale of Illegal Drugs Advances

FDA participated in a global operation to combat the sale and distribution of unapproved and illegal drugs.
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Will Interchangeability Boost Biosimilar Prescribing?

Biopharmaceutical companies have pressed hard for clarity on the testing and data required by FDA to gain market approval of biosimilars that can be filled by a pharmacist without prescriber preapproval.
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Industry News

ISPE 2017 Annual Meeting & Expo Keynote Speakers Announced

Keynote speakers for ISPE's 2017 Annual Meeting & Expo include representatives from AstraZeneca and GSK.
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Wuxi Medical Instrument Factory Receives FDA Warning Letter

Validation and batch testing failures were among the violations found by the FDA at the company's Jiangsu facility.
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Regulatory News

EMA Provides Update on Relocation Preparedness and Impact on Staff Retention

Staff survey on the relocation of EMA indicates that the future of public health in Europe is at stake.
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Preparing for the Inevitable: Key Steps for Weathering a Pharmaceutical Recall

Pharmaceutical companies should prepare for the impact of recalls to minimize risk to consumers and the company.
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More Regulatory News


Bio/Pharma News

AbbVie Partners with BMS for Combined Lung-Cancer Therapy

The collaboration will evaluate the combination of BMS' Opdivo immunotherapy with an investigational antibody drug conjugate in development by AbbVie.
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Merck & Co.'s Keytruda Gets FDA Approval for Gastric Cancer

This latest FDA approval expands the blockbuster anti-cancer biologic's indications in oncology.
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More Bio/Pharma News

Supplier News

Cambrex Adds Reactors to Facility in Sweden

Additional reactor capacity and a wastewater processing plant increase API manufacturing capacity at the Cambrex site in Kalskoga, Sweden.
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GE Launches New MAb Purification Resin

The new purification resin is expected to improve monoclonal antibody purification capacity by up to 40% due to its high binding capacity.
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FEATURED TOPICS

Analytics

Stepping Up the Pace of Drug Stability Studies

Forced degradation studies can identify stability problems for drug substance and drug products.
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Drug Delivery

Targeting the Lungs

Considerations in selecting a dosage form for drug delivery to the lungs.
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Formulation

Speeding Up Formulation Development

QbD principles and strategic thinking can reduce the time required to optimize formulation.
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MANUFACTURING

New Technologies Optimize API and Drug Product Manufacturing

Innovative new technologies released over the past several months seek to enhance bio/pharmaceutical development and manufacturing.
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Product Profile

Eurofins BioPharma Product Testing

GMP Laboratory Testing Services
Eurofins BioPharma Product Testing is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide providing comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies.
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Event Profile

CPhI Worldwide 2017

Date: 24-26 October 2017
Venue: Messe Frankfurt, Germany
CPhI Worldwide, together with co-located events ICSE, InnoPack, P-MEC and FDF, hosts more than 42,000 visiting pharma professionals over three days. 2,500+ exhibitors from 153 countries gather at the event to network and take advantage of more than 150 free industry seminars. The exhibition covers every sector of the pharmaceutical market under one roof.
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UPCOMING WEBCASTS

From Candidate to Clinic: Strategies to Select, Assess, Formulate, and Deliver the Right Drug Candidate in the Early Phase
Live Webcast: Tuesday, October 10 at 2:00pm EDT
Register now


Enteric Capsule Technologies to Help Fast-Track Pharmaceutical Drug Development
Live Webcast: Thursday, October 17 at 9am EDT
Register now


Excipient Selection to Enable the Performance of Skin Delivery Dosage Forms
Live Webcast: Wednesday, Oct. 18, 2017 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
Register now


ON DEMAND WEBCAST

No-Fuss Continued Process Verification: Automating Process and Product Monitoring
On Demand
Learn more


Events

CPhI Worldwide

Messe Frankfurt, Germany

24–26 October 2017


more events

eBOOKS

Biologics and Sterile Manufacturing

New technologies, including single-use systems, are leading the push for faster production and higher titers. At the same time, ensuring quality in raw materials and water systems, and controlling contamination are paramount. In this Biologics and Sterile Manufacturing eBook, the editors explore key technology, process, and operational topics.

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