Pharma Focus Europe-Newsletter

Pharma Focus Europe-Newsletter

Latest Articles

Access to Affordable Medicines: A Persistent Challenge for Europe

High accessibility to medicines is still a concern in Europe due to increasing costs and variability in price per country and a lack of legislation to mitigate the problem. The problem of high prices impacts a healthcare system and limits patients’ access to treatment. They are generic medicines promoted, starker pricing talks, and increased regional collaboration for permanent, non-discriminatory access to key medicines for each and every European.

Access to Affordable Medicines in Europe

Innovative Pricing Models in the EU: Making Medicines Affordable for All

In this article, we discuss new approaches to drug pricing in the EU: value-based pricing, risk sharing, subscription and differential pricing. These strategies are to achieve cost reduction for medicines now and in the future to be more affordable, sustained and accessible, and to advance pharmaceutical innovation. Future trends, opportunities and threats such as regulation and structuring of data are also examined.

Innovative Pricing Models in the EU

The 2025 Agenda: Navigating New European Compliance Challenges in Pharma

The compliance of the European pharmaceutical industry comes with complex works in 2025 as pharmacovigilance, sustainability requirements, clinical trial regulations, data protection regulation, and supply chain regulation. This article focuses on these challenges and provides practical future steps using available technologies and teamwork to overcome them while keeping up with current state and federal laws.

Navigating New European Compliance Challenges in Pharma

The Top 15 Pharma Blogs and Publications in the World

To the extent that it is recognized as a vital source of information, the pharmaceutical industry relies heavily on credible blogs and publications. These platforms not only provide insights into the latest research and trends, but also foster discussions that can influence policy and practice within the healthcare sector.

Top 15 Pharma Blogs and Publications in the World

Stay updated with the latest articles.


Expert Interviews

Effective Management of the Development and Clinical Drug Supply in the Pharmaceutical Industry

Author: Arul Joseph PhD MBA, Senior Director of Pharmaceutical Development at Otsuka Pharmaceutical Companies (U.S.)

We asked Arul Joseph to share his thoughts on how to effectively manage the pharmaceutical development and manufacturing of drug substances and drug products to meet clinical supply needs from the early to late stages of development in the pharmaceutical industry.

Balancing Innovation and Risk Management in R&D

Author: Kishore Hotha, PhD, MBA, President, Dr.Hotha's Life Sciences LLC

Biotech, CDMOs, and big pharma must collaborate strategically to balance innovation with risk management in R&D. By combining biotech’s agility, CDMOs' specialized expertise, and big pharma’s robust risk frameworks, they can efficiently and safely navigate drug development, ensuring groundbreaking therapies advance from discovery to commercialization.

Balancing Innovation and Risk Management in R&D

Data-driven Marketing Approaches

Author: Preetha Vasanji, President-Emerging Markets, Doceree

Can you provide an overview of your journey in the healthcare communications and marketing sector?

My journey in healthcare communications and marketing began at McCann Health in Mumbai about two decades ago, where I eventually became the general manager, leading a team of over 30 professionals. I met many extraordinary minds there, one of which was Harshit Jain, MD. I joined him in his venture, Doceree, in 2020.

Data-driven Marketing Approaches

Access additional expert interviews.


Industrial Events

World Congress on Pharmacology and Drug Safety

World Congress on Pharmacology and Drug Safety

Pharmapack Europe

Pharmapack Europe

9th Microbiome Movement Summit Europe

9th Microbiome Movement Summit Europe

Discover additional industrial events.


Industrial Projects

Merck Invests €70 Million to Expand ADC Manufacturing for Cancer Therapies in the U.S.

Merck Company has announced €70 million to expand its ADC manufacturing capabilities in the USA. This expansion will significantly increase capacity, tripling the current levels, and strengthen the company’s contract development and manufacturing organization (CDMO) services, reaffirming its dedication to supporting clients and patients.

Piramal Pharma Invests $80 Million to Expand Sterile Injectable Facility in Kentucky

Piramal Pharma Solutions (PPS) is investing $80M to expand its Lexington, Kentucky facility. This site specializes in sterile injectable drug products, including compounding, liquid filling, and lyophilization. The expansion will support PPS's ADCelerate? program for antibody-drug conjugates and enhance capacity to meet growing market demand.

AstraZeneca Invests $3.5 Billion to Expand R&D and Manufacturing in the U.S

AstraZeneca has unveiled plans for a $3.5 billion capital investment in the United States to enhance its research and manufacturing capabilities. This initiative includes $2 billion allocated to new projects, which are set to generate over a thousand high-skilled jobs, bolstering the U.S. economy.

Explore more industrial projects.


Most Engaging Articles

Strategies for Securing Pharma Manufacturing’s Fast-expanding Data Landscape

Author: Juan José L., Associate Director of Cyber Security Architecture and Governance, Life Sciences Manufacturing, Cognizant

In this article, Juan Jose Lopez, Associate Director of Cyber Security Architecture and Governance, Life Sciences Manufacturing at Cognizant, will explore the challenges of AI and how companies can overcome them to effectively harness AI to keep safe their most valuable asset—their data.

Strategies for Securing Pharma Manufacturing

The Pharmacovigilance IT Ecosystem: A Key to Patient Safety

Author: Vikalp Khare, Director, Otsuka Pharmaceutical Companies (U.S.)

This article explores the details of a typical pharmacovigilance (PV) information technology ecosystem setup & maintenance, which is essential for any pharmaceutical company to ensure the safety of the patients consuming their medicinal products. The article also touches upon a possible controlled approach of leveraging AI & ML to establish an efficient, effective & cost-benefiting PV-IT ecosystem.

Pharmacovigilance IT Ecosystem

Dissolution Profiles Comparison: New EMA Recommendations

Author: Marek Skowronek, Quality Systems Manager, StatSoft Polska

The article presents recent EMA recommendations and proposed methods for comparing dissolution profiles, particularly when the prerequisites for the standard f2 similarity factor method are not met. A method selection scheme is discussed, supported by case studies that highlight the advantages and disadvantages of various dissolution profile methods, along with practical insights.

Dissolution Profiles Comparison

Discover the most engaging articles


Press Releases

U.S. Food and Drug Administration issues Complete Response Letter for the glepaglutide New Drug Application for the treatment of short bowel syndrome

Quoin Pharmaceuticals Announces FDA Clearance to Initiate New QRX003 Netherton Syndrome Clinical Study

Immunovia CEO and board members announce intention to fully exercise their TO2 warrants

Praxis Precision Medicines Announces Rare Pediatric Disease Designation Granted for Relutrigine in Dravet Syndrome

View additional press releases.


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