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eLife Sciences

eCValidation at DIA Europe 2024

In just one week, we’ll be attending DIA Europe 2024 in Brussels! We would love for you to join us at our presentation in Innovation Hub 2. Topic: Advancing Regulatory Practices and Pharmacovigilance through Industry 4.0: A Detailed AnalysisSpeaker: Michał Timler, Director of Validation Business Unit Overview: The adoption of

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eConsulting at the XIV World Congress of the Pharmaceutical Industry

Today marks one of the key events in the pharmaceutical sector – the XIV World Congress of the Pharmaceutical Industry. This exceptional gathering provides an invaluable chance to explore cutting-edge advancements in technology, raw materials, packaging innovations, and the latest trends shaping the industry. We’re excited to be a part

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Validation of Computerized Systems in a Pharmaceutical Wholesaler

Pharmaceutical wholesalers rely more and more on advanced IT systems for the storage, management and distribution of medicinal products. The introduction of information technology in the pharmaceutical industry has brought many benefits, but at the same time imposes responsibility for ensuring the security, effectiveness and compliance with regulations of these systems.

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Process Validation in a Pharmaceutical Wholesaler

Pharmaceutical supply chains are inextricably linked to Good Distribution Practices, Good Manufacturing Practices, and the Code of Federal Regulation; these regulations and guidelines ensure that pharmaceutical products are distributed according to appropriate standards and with safety. One of the key elements of ensuring safety and quality in pharmaceutical wholesalers is process validation.

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