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Innovations and highlights in the Pharma industry 

Dive deep into the world of Pharma with Zamann’s Expert Blog. Our industry-leading professionals share insights on global project management, quality consultancy, digitalization, and more. Stay updated with trends and innovations transforming the Pharma industry. 

News and more

Copy-Paste Chaos in the Lab? Batch Templates in LabWare 8 Save You

Many pharmaceutical labs repeatedly re-enter identical equipment, reagents, and standards for each lot in the LIMS, creating inefficiency and data integrity risks. Copy-paste errors lead to reagent mix-ups, incorrect instrument assignments, deviations, and delays. LabWare 8 batch templates let labs
  • Blog

Lot Release Without Full Review? LabWare 8 Stops the Risk

Lot release is the most critical step in pharmaceutical quality management, yet lots are sometimes released before all samples and tests are reviewed and approved. This practice jeopardizes data integrity, invites inspection findings, and risks patient safety. LabWare 8 enables
  • Blog

Kill the Redundancy: Why Environmental Monitoring Belongs Inside LabWare LIMS 8

Running a LIMS and a separate environmental monitoring (EM) tool often feels fine—until the bill for the second stack shows up in licenses, servers, validation cycles, and the time your teams spend reconciling data.
  • Blog

ISO 9001 2026: What You Need to Know

The ISO 9001 2026 revision is underway, introducing modern elements such as digital systems, ESG principles, and enhanced risk and resilience guidance. This article provides an overview of the upcoming changes and what organizations should expect.
  • ISO 9001, Quality Management System
Achieve operational excellence by building a strong foundation of equipment qualification documentation and protocols.

Why CAPA Effectiveness Checks Are More Important Than Ever in Pharma

The pharmaceutical industry is under growing scrutiny from regulators when it comes to CAPA effectiveness checks. This blog explores how to improve root cause analysis, ensure closed-loop CAPA systems, and avoid repeat findings in GMP audits.
  • Audit and Inspection, Quality Management System
scientist conducting an audit of the company

IVDR Transition: A Real Test for QA Teams

The IVDR transition is reshaping the EU diagnostics industry. This post explores how QA teams can handle real challenges during implementation—especially for Class B and C IVDs—while staying compliant with UDI, PMS, and performance evaluation requirements.
  • MD/IVD Regulations, Medical Devices, Technical Documentation
Doctor with digital medical device

Medical Device Clinical Trials – What You Need to Know in 2025

Understanding how clinical trials for medical devices are designed, conducted, and evaluated is critical in a highly regulated market. Here’s a clear, current, and professional look into the world of medical device clinical trials in 2025.
  • MD/IVD Regulations, Medical Devices
Female doctor looking at transparent tablet with medical digital diagnostic screen

Working Standards in Pharma: Ensuring Quality and Compliance

Discover how working standards uphold quality, safety, and regulatory compliance in the pharmaceutical industry. Explore key components and best practices.
  • GxP, Quality Management System
The lifecycle of a working standard involves several stages