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14 December 2018 | By ACG
This webinar focuses on the benefits of integrated pharma manufacturing using examples of integrated processing and packaging solutions. The webinar will also highlight the key advantages of choosing a single pharma solutions provider for all manufacturing needs...
Fundamentals. The drab cousins of the headline grabbers like AI or Pharma 4.0. But focusing on them can be the investment that offers the most long-term rewards for companies in terms of risk mitigation, cost reduction and improved overall agility. In pharmaceutical packaging and labelling, the key fundamental is the…
Find out more about PQE Group services from our Vice President and Partner Danilo Neri at last PharmaLab 2018 in Dusseldorf.
In an all-time record year for FDA approvals (48 so far in 2018), Pharmapack Europe reports that innovation is also accelerating across the drug delivery and packaging industries...
On 23 June 2016, the decision was made on the European Union referendum for the United Kingdom to withdraw from the European Union.
The FDA requires drugs to be tested on children after they have been approved for adults, however two thirds of these are not happening...
A report has analysed the temperature controlled pharmaceutical packaging market, with forecasts on various market areas up until 2025...
Eurofins BioPharma Product Testing’s facilities deliver the world’s most comprehensive scope of harmonized GMP testing services and seamless regulatory acceptance.
With just under one month until the Drug Supply Chain Security Act is enforced in the US, manufacturers are still not all compliant with the rulings...
In this Spotlight on Continuous Manufacturing, MG2 explains why they are the single partner clients need for all productions into hard-shell capsules...
Pharmaceutical service provider relies on expanded capacities, modular production and modern analytics...
In this issue: LC-MS multi-attribute methods for the characterising and QC testing therapeutics, integrating data from Quality Control and Production to enable fast and informed decisions, and Solid-state NMR spectroscopy: using freeze drying to predict the stability of biological products.
We are pleased to announce the appointment of Ludo Gielen as new Chief Executive Officer of Schoeller Allibert effective 01 November 2018...
Dr Scott Gottlieb highlighted how brand reference drug companies voluntarily withdraw their marketing applications and stopped updating their labelling...
5 October 2018 | By PerkinElmer
The control of impurities plays a crucial role in Pharma QA/QC and can be divided in 3 main buckets: Organic, Inorganic and Residual Solvents. On this webinar we are focusing on analytical techniques used for control of Inorganic impurities and Residual Solvents...
