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PharmTech Europe
16 May 2017

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Top Stories

Compounding Pharmacy Cited for Unlicensed Biologics

FDA sent a warning letter to Pharmaceutic Labs, LLC for deficiencies in producing sterile drugs.
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Improving Productivity to Drive Drug Discoveries to Patients

Biomedical researcher shares insights from a career dedicated to advancing therapeutic innovations for unmet medical needs.
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Thermo Fisher Scientific to Acquire Patheon

Thermo Fisher will acquire Patheon for approximately $7.2 billion, including the assumption of approximately $2 billion of net debt.
/ read more /

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Industry News

WHO Launches Biosimilar Pilot Program

The program aims to make biosimilars for the treatment of cancer more widely available in middle- and low-income countries.
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US Prescription Drug Spending to Hit $610 billion in 2021, according to Quintiles/IMS

Forecasts were lowered, Reuters reported, due to reduced drug approvals and increased competitive pressures.
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Regulatory News

EMA Promotes Understanding and Use of Biosimilars

EMA and the European Commission released a biosimilars information guide for health professionals during the EC's biosimilars conference.
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The Complexity of IDMP

Many pharmaceutical companies are sceptical about IDMP despite the business benefits and its contribution to patient safety.
/ read more /


More Regulatory News

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Bio/Pharma News

Novartis Licenses CAR-T Patents in Separate Deals

Novartis entered separate license agreements with bluebird bio and Celyad for patents related to the manufacture of CAR-T cells.
/ read more /


Oxford Genetics Licenses CRISPR Gene Editing Technology from ERS Genomics

Licensing agreement will expand Oxford Genetics bio-therapeutic discovery, design, and development service business.
/ read more /


More Bio/Pharma News

Supplier News

Croda Completes Global EXCiPACT Accreditation

The company is the first multi-site excipient supplier to achieve accreditation across production facilities.
/ read more /


API from Unregistered Companies Entered US, According to FDA

The agency sent a warning letter to Sal Pharma for not disclosing information about API manufacturers to customers.
/ read more /


More Supplier News

FEATURED TOPICS

FILL/FINISH

Impact of PFS and Filling Process Selection on Biologic Product Stability

The author discusses the impact of prefilled syringe product contact materials and the filling and stoppering process on protein aggregates.
/ read more /

 

ANALYTICS

Solid-Phase Extraction for the Preparation of Aqueous Sample Matrices for Gas Chromatographic Analysis in Extractable/Leachable Studies

Solid-phase extraction has several advantages over liquid/liquid extraction for extractables and leachables studies.
/ read more /

PACKAGING

Robots Package Parenteral Products

Robotic fill/finish systems reduce human intervention, improve flexibility, and allow more gentle handling of containers.
/ read more /

MANUFACTURING

Optimizing Yields on Modern Tablet Presses

Learn how to prevent common causes of product loss.
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Product Profile

Aptar Pharma

Aptar Pharma Partners with Kali Care to Develop Real-Time Medication Management Technology
Aptar Pharma and Kali Care have announced that they entered into a partnership in order to address the challenge of monitoring adherence in ophthalmic clinical trials.
/ Read more/


UPCOMING WEBCAST

Best Practices for Extractables and Leachables Testing for Primary Drug Product Packaging
Live Webcast: Wednesday, May 24 at 11:00am EDT and Wednesday, May 31 at 11:00am CEST
Register now



ON DEMAND WEBCASTS

A Complete Guide to USP <232> & <233> Pharmaceutical Elemental Impurities – Understanding Pharmaceutical Elemental Impurity Regulations and Laboratory Considerations
On Demand
Learn more


A Complete Guide to USP <232> & <233> Pharmaceutical Elemental Impurities – Implementing Pharmaceutical Elemental Impurity Sample Preparation and Analysis
On Demand
Learn more


Events

CPhI North Amercia

Philadelphia, United States

16–18 May 2017

Pharmaceutical Sciences World Congress

Stockholm, Sweden

21–24 May 2017

1st Seminar on Formulation Designs for Challenging Needs

London, United Kingdom

22 June 2017


more events

Reference Library

Pharmaceutical Technology Outsourcing Guide

Pharmaceutical Technology Outsourcing Guide provides details behind recent partnerships, strategies for selecting an appropriate CDMO/CMO, and quality by design factors for outsourced operations.
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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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