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Leveraging synergies in pre-clinical biomedical R&D – pharmaceutical companies benefit from new innovation models

Introduction: As the complexity of pharmaceutical research and development increases constantly, its innovation productivity defined as the successful approval and launch of truly novel drugs and therapies, has declined since years. To boost its innovation productivity,the pharma industry has...

Ensuring Regulatory Compliance in Pharmaceutical Manufacturing

Introduction: Quality control laboratories play a vital role in pharmaceutical manufacturing, from the evaluation of raw materials through to the release of the final packaged product. They are pivotal in ensuring the safety and efficacy of products administered to...

An Overview of Russia’s Pharma Serialization Regulations and its National Track and Trace Digital System, Chestny ZNAK

Introduction: Russia began transforming its pharma supply chain on December 29, 2017, when President Vladimir Putin signed Federal LawNo.425-FZ. This legislation aims to streamline the quality control of pharmaceuticals, protect against counterfeit medicines, and monitor supply, demand, and expenditure. Phased implementation...

Putting the Patient First: Not Just When It’s Convenient

Introduction Successful clinical trials rely on effective patient recruitment and retention. However, a 2019 report indicates that the industry continues to struggle meeting these objectives. The study found that about 80 percent of clinical trials don’t meet patient enrollment deadlines,...

Scientific data Management – the crucial importance of laboratories

Few weeks have passed between the day I have been in contact with World Pharma Today to prepare this article and the date of the submission. In just few weeks the world has dramatically changed. Working from home as about...

The unexpected benefits of clinical trial disclosure

Introduction: Patients, clinical trial sponsors and institutions are starting to benefit from increased transparency commitments and significant investments in trial data disclosure. To make an ever-broader scope of trial data public, leading pharmaceutical organizations have been refining their processes and...

Biopharma Freight in Asia: Growing Cost Pressures Drive Smarter Risk Management

How can logistics professionals manage costs without creating unnecessary risks on the biopharma cold chain? Here are a few tips for planning freight shipments in and out of Asia. As bio-pharmaceutical production accelerates in Asia, global manufacturers are becoming increasingly...

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