Clinical trials have grown increasingly complex and now require robust solutions to manage data, documentation, and workflows. Traditionally, organizations have relied on separate systems for Clinical Trial Management Systems (CTMS) and Electronic Trial Master Files (eTMF), often leading to inefficiencies, compliance risks, and administrative burdens. An all-in-one eClinical tool that integrates CTMS and eTMF offers a seamless solution, and improves trial efficiency, ensures regulatory compliance, and optimizes resource use. This article explores the benefits of adopting an integrated platform ..read more

In the fast-paced and highly regulated medical device industry, engineering services play a critical role in helping companies develop safe, effective, and compliant products. Whether a medical device company is designing a new device, improving an existing product, or navigating the complex regulatory landscape, engineering expertise is essential at every stage of the product lifecycle. In this article, we’ll explore the key questions medical device companies may ask when considering engineering services, how these services can help, and when they might need them. What Questions Would Medical ..read more

Have you ever wondered how life-saving treatments for cancer, Alzheimer’s, or chronic diseases come to life? Clinical trials are the foundation of medical innovation, paving the way for groundbreaking therapies. Yet for many, the idea of joining a trial can feel intimidating or unclear.  Experts are here to demystify the clinical trial process, with Dr. Frances Broyles and Dr. Sheryl Marks of Rainier Clinical Research Center offering valuable insights to help you make an informed decision about participating in this critical step toward advancing healthcare. 1. Understand the Cl ..read more

CPHI Milan – the world’s largest pharma event – hosted last month in Milan saw a new record attendance of 59,000 pharma executives buoyed by returning confidence and increased deal-making on site. The post Pharma prepares for CDMO growth in 2025 as CPHI Milan reports record attendance appeared first on Pharma Mirror Magazine ..read more

In healthcare, safety is always the top priority—whether it's protecting patients or the staff who care for them. Personal protective equipment (PPE) plays a vital role in ensuring this safety, and one item that stands out is nitrile exam gloves. The post Why Nitrile Exam Gloves Are the Preferred Choice for Medical Professionals appeared first on Pharma Mirror Magazine ..read more

The pharmaceutical industry is constantly shifting, as consumers seek the best treatments. As the market demands new solutions, drugmakers are tasked with investing heavily in research, development, manufacturing and commercialization. Meeting the needs of the sector can be challenging, especially for companies that don’t have the necessary resources. Contract Development and Manufacturing Organizations (CDMOs) offer practical solutions. CDMOs, which originally only acted as service providers, have become integral in driving innovation in the pharmaceutical industry. These specialized entities ..read more

Ensuring the safety and efficacy of pharmaceutical products is paramount in the healthcare industry. Pharmaceutical impurity reference standards play a critical role in this process by helping to identify and quantify impurities. Understanding their importance can significantly enhance quality control measures in drug development and production. In today’s pharmaceutical industry, maintaining high-quality standards is not just a regulatory requirement but also an ethical obligation. As you delve into the complexities of drug development, the significance of impurity reference standards becomes ..read more

By Michael von Papen, Chief Expert at Pharmatec GmbH – a Syntegon Company When a leading global collagenase manufacturer wants to renew and optimize a system at the heart of its production, technical expertise, and engineering competence is paramount. Moreover, cooperation within the project team needs to be well organized. Nordmark and Pharmatec, a subsidiary of Syntegon, have shown how this helps to master even unexpected challenges during the construction of a new filtration and concentration system for collagenase. With 650 employees, Nordmark Pharma, based in Uetersen, Germany, is not one ..read more

By Justin Kozak, Executive VP & Life Sciences Lead, Founder Shield The tide is turning in the once-booming biotech industry. Funding slowdowns and heightened competition are forcing companies to re-evaluate their strategies. Restructuring, including mergers and acquisitions (M&As) as well as workforce adjustments, has become a common theme. In this shifting environment, proactive risk management and strategic planning are crucial for biotech leaders. This post reviews solutions to help companies navigate these challenges, build resilience, and secure their long-term succ ..read more

Addiction is affecting a large portion of people’s lives at the minute, but one of the things people often struggle with is knowing how to afford rehab. There’s a common misconception that it costs thousands upon thousands of pounds and is entirely unattainable for people in some circles of society. However, that’s precisely what it is, a misconception, and many options can help people, no matter how wealthy or poor they are. The question of ‘how much does rehab cost in the UK?’ comes up a lot, but ultimately that depends on various circumstances, including how long you’re there for The post F ..read more