news
Antalis drives forward with new vehicle fleet
Antalis’ customers are set to benefit from a fleet of more technologically advanced vehicles as part of its £5m partnership with fleet provider, Fraikin...
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Packaging & Labelling
news
Patheon to invest $45 million in spray drying & manufacturing solutions
Patheon expects to invest approximately $45 million at key sites across its network in spray drying capabilities and flexible manufacturing solutions...
whitepaper
Whitepaper: Extractable and leachables studies – designed and performed to meet all intended needs
Following FDA legislation in 1999, scrutinising packaging standards for extractables and leachables has become the norm. In this whitepaper, Eurofins examines the ways in which the evaluation of final packaging components is now carried out including the role of liquid and gas chromatography-mass spectrometry in the process.
article
Personalised medicine, batch size of ONE, the new challenge to fill-finish?
Wenzel Novak PhD gives some considerations on container, environment, process and automation for small batch sizes in the downstream process of fill-finish…
article
Issue #3 2017 – Digital version
In Issue #3 2017: In-Depth Focuses covering Raman Spectroscopy, Separations & Purifications, Formulation Development & Delivery; Guide To Testing Services; GMP and mutual recognition; Regulatory Insight; RMMs; Microbiology Series; and much more...
news
Antalis Packaging warns of quality control amid corrugated price hikes
15 May 2017 | By Niamh Marriott, Junior Editor
Antalis Packaging says that it is now more important than ever for companies to be watchful on their corrugated box specification and quality...
article
Does the Falsified Medicines Directive lead to a European pack coding guideline?
The Directive on Falsified Medicines (FMD, or Directive 2011/62/EU amending Directive 2001/83/EC) and its supplementing Delegated Regulation (DR 2016/161) aim to improve patient safety by preventing falsified medicines from entering the legal supply chain...
article
Strategic aspects of change control for pharmaceutical packaging systems
Plastic materials used in pharmaceutical packaging can interact with the packaged dosage form, causing leachables to accumulate...
article
FMD and supply chain security
Over 12 months ago, the European Union delegated regulation that supplements the Falsified Medicines Directive (FMD) was published in the Official Journal of the European Union, starting the countdown to the deadline of 9 February 2019, when most EU member-states, and three non-members currently, are expected to have implemented all…
article
Issue #2 2017 – Digital version
Read the free-to-view digital version of the latest issue of European Pharmaceutical Review...
article
Packaging In-Depth Focus 2017
FMD and supply chain security; Strategic aspects of change control for pharmaceutical packaging systems; and does the Falsified Medicines Directive lead to a European pack coding guideline?
news
Lonza to host new webinar: “Justifying a paperless solution – building a compelling business case”
Lonza is hosting a free 60-minute webinar on 25 April 2017 on how to create a compelling business case for the implementation of a paperless QC testing solution.
news
Discover the Rainin SmartStand™, the world’s first intelligent pipette stand
29 March 2017 | By Mettler Toledo Rainin, LLC
METTLER TOLEDO’s recently launched Rainin SmartStand™ is set to transform pipette management...
article
Issue #1 2017 – Digital version
Read the free-to-view digital version of the latest issue of European Pharmaceutical Review...
webinar
SIFT-MS: A New Tool for Impurity Profiling in Pharmaceutical Products
21 February 2017 | By Syft Technologies
SIFT-MS is a new tool for real-time, selective and economical trace gas and headspace analysis. SIFT-MS uses soft chemical ionisation to quantify volatile compounds, including chromatographically challenging ones such as formaldehyde, formic acid, and ammonia...
