Felicity Thomas is the former Associate Editorial Director of Pharmaceutical Technology, Pharmaceutical Technology Europe, BioPharm International.
Waters Set for Growth in Bioanalytical Characterization with Wyatt Acquisition
Waters Corporation expected to boost growth in bioanalytical characterization for new modalities with acquisition of Wyatt Technology.
Keeping Up with Tablet Tooling Maintenance
A good understanding of tablet tooling and how to properly maintain these key parts will maximize lifespan of tools.
EC Authorizes Fabry Disease Treatment
EC has granted marketing authorization to Chiesi Global Rare Diseases and Protalix BioTherapeutics for PRX-102 (pegunigalsidase alfa).
Biosynth Acquires Cambridge Research Biochemicals
Critical raw materials supplier, Biosynth, has acquired UK-based Cambridge Research Biochemicals (CRB).
Vetter Prepares to Further Increase Production Capacity and Services at Austrian Site
Vetter is further expanding its production capacity and services at its Rankweil, Austria site.
Optimizing the Manufacture of Emerging Therapies
Guidance for GMP manufacture of emerging therapies has evolved to accommodate innovation and the broader spectrum of products in development, but greater harmonization is still needed.
On Strike!
Strike action is impacting numerous sectors across Europe, including the bio/pharma industry.
Drug Solutions Podcast: Considering Biologic Drug Development and Manufacturing Holistically
In this episode, Hanns-Christian Mahler and Andrea Allmendinger from ten23 health will discuss some key aspects of biologic drug development and manufacturing.
Balancing Change and Certainty in Manufacturing
As new manufacturing processes and technologies are introduced to meet demand and overcome challenges, understanding also needs to improve to ensure the right balance is achieved.
Formulating Drugs for Continuous Processing
Despite the advantages intensified processes can offer developers, there are still some obstacles to overcome before broader application of new technologies will be implemented.
Accepting Alternative Approaches to Freeze Drying
Alternative approaches to freeze-drying are gaining popularity and will help to overcome some of the challenges associated with conventional lyophilization.
Legislative Hold-Up
A further setback to the publication of the pharmaceutical legislative changes in Europe may mean time is running out for appropriate review before 2024 parliamentary elections.
Drug Solutions Podcast: How CROs Adapt Themselves in the Ever-Changing Landscape of Cell and Gene Therapies
In this episode, Rhonda Henry and Adam Mendizabal from Emmes discuss the role CROs play in cell and gene therapies undergoing clinical trials at all stages.
Influencing Change in Drug Delivery
Advancements in therapeutic modalities are necessitating change in drug delivery to help negate some of the expense of development and manufacturing.
Keeping Europe’s Medicines Stocked
Technological advances will help ease pressure on pharma supply chains, allowing for greater visibility and less uncertainty.
Feeling the Pinch
Soaring energy costs are compounding the challenges currently being faced by the European bio/pharma industry.
Drug Solutions Podcast: Progressing Excipients Through Review
In this episode, Ana Ladino provides an update on the acceptance of a novel excipient onto CDER’s pilot program.
CROs Gaining a Competitive Edge
Shifting toward more technological solutions and ensuring a greater understanding of the workforce’s needs will give both CROs and sponsors a market advantage.
Advantageous Positioning for Europe in Pharmaceutical Cannabis
The European bio/pharma industry’s high regulatory standards and GMP requirements are set to position the region as a frontrunner for pharmaceutical‑grade manufacturing of cannabis-based medicines.
Improving Gender Diversity
Although some headway is being made into more gender-diverse executive levels in pharma, much more work is still needed.
Validating Cleaning Methods in Bio/Pharma Processes
Analytical techniques for validating cleaning methods must evolve to match the pace of an increasingly complex manufacturing landscape for new therapeutics.
Providing a Snapshot of the Industry
CRB’s latest industry report includes an expanded audience to include many European countries, which has provided some interesting insights.
Opening Up Opportunities in 2023
Bio/pharma has evolved and adapted to a variety of challenges in 2022, but what might be on the cards for the industry in 2023?
Cleaning Up in Bio/Pharma
As the therapeutic landscape grows more complex, so too must the analytical techniques for cleaning validation to ensure the utmost cleanliness is achieved.
Setting Goals for Sustainability
In light of increasingly stringent sustainability requirements, bio/pharma companies need to make sure they formulate effective ESG strategies.
Getting Personal for Blockbusters in 2023
The latest report from Clarivate has been published, highlighting 15 potential blockbusters to watch out for in 2023, the majority of which are personalized medicines.
Agilent Sets Up Dissolution Testing Hub in UK
Pharmaceutical Technology Europe got the scoop on Agilent's new Dissolution Testing Centre of Excellence in Craven Arms, UK.
Building Up to a Bright Future
Dissolution testing is experiencing a refresh thanks to a variety of market drivers.
The Next Blockbuster
Anti-obesity drugs have the potential to be the next blockbusters, according to market analysis.
Putting a Spotlight on Particle Engineering
Opportunities and developments in particle engineering are providing developers with the tools to advance drug candidates successfully.