Felicity Thomas is Associate Editorial Director of Pharmaceutical Technology, Pharmaceutical Technology Europe, BioPharm International.
Better Connected: The Value of Connected Drug Delivery
Connected delivery solutions can provide value to industry and patients, through improved medication adherence and outcome optimization.
Securing the Supply Chain
The global COVID-19 pandemic has highlighted the need for the pharmaceutical industry to strengthen its supply chain.
A Little More Respect
Pharma’s reputation is being boosted in light of the current COVID-19 pandemic efforts.
On Point: Biologics Drive Growth in Pre-Filled Syringes
As a result of the rising use and development of biological drugs, the biopharma industry is witnessing an increase in the adoption of prefilled syringes.
Complying Confidently? Learning Lessons from Nitrosamine Impurities
Industry must never become complacent about the safety of drug products and should seek to continually perform surveillance even if the drug is well-established.
Can We Teach an Old Drug New Tricks?
In light of the hype around chloroquine and hydroxychloroquine as potential COVID-19 treatments, it is important to remember that drug repurposing should never be rushed, irrespective of the urgency of the situation.
A Welcome Change: The Benefits of Reformulation
Reformulation strategies can provide drug developers with a head start to achieve promising options that benefit the patient.
Keeping Aggregation Under Control
Characterizing and controlling protein aggregation is vital to ensure safety and efficacy of a biopharmaceutical product. In this interview, important aspects of protein aggregation and the tools available to address this issue are discussed.
Making Every Effort
As COVID-19 rapidly spreads, the bio/pharma industry is committing significant efforts to fast track development of therapies.
Avoiding Negative Drug–Device Interactions
Considering the potential interaction of a drug with the delivery device early on in in development is integral to achieving the best combination.
Delivering the Goods
The new molecules entering the development pipeline are bringing forth exciting challenges in drug delivery.
A Little Thought Goes a Long Way in Tableting
Understanding formulation properties early in development can prevent some costly issues later on.
In Top Tablet Form
OSD forms are popular within the industry due to the various advantages they offer, but there are specific considerations required to get the best OSD form possible.
Stability Testing: The Crucial Development Step
As compounds become more complex in nature and biological ingredients are more widely used, stability testing approaches must follow suit and provide flexibility for developers.
Keeping Toxicity to a Minimum
Assays can provide a useful tool in determining the potential toxicity of drugs throughout the development cycle.
Noteworthy Historical Cases of Adverse Drug Reactions
A brief overview of three notable cases of adverse drug reactions.
The High Price of R&D
Despite increasing R&D budgets by bio/pharma companies, returns on this investment are reducing and the cost of bringing an asset to market is increasing.
Going with the Flow
Metrology has the potential to not only prevent harm to patients but also to support innovative therapeutic options.
The Benefits of Outsourcing Stability Testing
Outsourcing stability testing to full-service providers can offer comprehensive benefits to bio/pharma companies.
By Popular Demand: The Growth of Biopharma Outsourcing
The huge potential of biopharma is presenting an important epoch for outsourcing partners that can support the development and manufacture of biologics in an efficient way.
Stability Testing: The Critical Development Phase
As compounds become more multifaceted and biological ingredients are more commonly utilized, stability testing tactics must follow suit and ensure flexibility for developers.
Metrology has the potential to not only avoid damage to patients but also to encourage novel therapeutic opportunities.
Of Serious Concern?
Amid the rapidly rising cases of a novel coronavirus, concerns are being raised over preparedness and potential disruptions to the pharma supply chain.
Improving Solubility of Cannabinoids
Lipid-based solutions offer a natural approach to improving the solubility of cannabinoid-derived products.
Sourcing Success in Cell and Gene Therapy Development
As cell and gene therapies become more prominent, industry is seeking the expertise and capabilities of outsourcing partners to ensure success.
Understanding Evolving E&L Regulations
Drug companies will have to sharpen their understanding of evolving E&L regulatory expectations in order to remain compliant.
Fresh Thinking in Biologic Drug Formulation
Biologics raise unique formulation and development challenges, and industry is still on a learning curve to get the best out of these diverse and complex therapies.
Pharma’s Decade in Brief
As a new decade has begun, this editorial reviews some of the biggest, brightest, and boldest happenings from the industry over the past 10 years.
On Trend in Pharma Packaging
Regulatory mandates, niche diseases, and patient-centric solutions have all impacted pharma packaging over the years and are expected to help shape the future of the sector.
Packing a Punch in Paris
PTE looks ahead to 2020’s edition of Pharmapack-the pharma industry’s dedicated packaging and drug delivery event.