Pharma Quality Exchange

Created and shared by industry experts, this global information and events platform is a must for all involved in pharmaceutical manufacturing.


  • Data Integrity in the Pharmaceutical Industry

    Expert Talk
    The reliability and integrity of pharmaceutical data is fundamental for regulatory compliance and consumer safety. Preserving data integrity, from initial gathering through traceable data transfer to safe storage in pharmaceutical manufacturing, is essential. Although, manual record keeping and transcription is a common way of documenting data, it is also one of the major sources of error and other data integrity violations. In the latest of a...
  • Know How - Design Pharmaceutical Qualification Processes Efficiently

    Expert Talk
    An interview with GMP expert Ralf Gengenbach, gempex GmbH The question of whether pharmacists implement GMP compliant qualification of production facilities or the validation of associated processes...
  • A New Guide for Effective Customer-Supplier Partnerships

    A New Guide for Effective Customer-Supplier Partnerships

    The ECA Good Practice Guide distills government guidance into a slim but comprehensive guide Since the first mother of all validation guidelines in 1987, different methods for pharmaceutical equipmen...
  • What Quality Agreements Exist for Pharmaceutical Outsourcing?

    What Quality Agreements Exist for Pharmaceutical Outsourcing?

    In the pharmaceutical industry, many factory production processes are outsourced to Contract Manufacturing Organizations (CMOs). This is often to circumvent capacity problems in their own plants, to ...


  • Effective Service Through the Life of Your Equipment

    Service approaches to maximize product inspection equipment effectiveness Product inspection equipment supports compliance with product safety standards and regulations. However, the equipment is only one piece of the puzzle. Without a strong service plan, any investment in product inspection equipment could fail to provide the best results. Service needs vary according to the application and production requirements. However, limiting downtime...
  • Five Key Steps to Improve Product Inspection of Liquid Pharmaceuticals

    Thanks in part to an increased demand for biologics and cancer drugs, liquid pharmaceuticals have recently experienced strong growth in the pharma industry. As a manufacturer, an incorrect dosage or ...
  • Accelerate Your Lab Weighing Through Digitalization

    Tips and tricks for completeness and traceability of your lab data The digital world is spinning faster and faster. Don’t wait, take a leap and accelerate your electronic lab data management today! E...
  • Meeting Traceability Requirements in Vaccine Production

    Never before have pharmaceutical companies and research institutions reacted as quickly to a new pathogen as they did to the new coronavirus Sars-CoV-2. With the demand to quickly produce and distrib...


  • Why Code Checks Are Important

    Have you ever had to wait longer than usual in a supermarket line because a barcode couldn't be scanned at the checkout? This has probably happened to each of us at some point and is not only annoying for us as waiting customers, but also for the cashier who may have to deal with several such problems every day. For this reason, vision inspection systems are designed to reject products with poorly printed or unreadable codes from the production ...
  • Pharmacopeia Regulations for Pharma Waters

    Controlling the Risk of Contamination in Real-Time in Pharmaceutical Waters In this hour long webinar, Jim Cannon, an expert in global pharmaceutical water regulations, shares his knowledge on recent...
  • Vision Inspection for Quality Assurance in Cosmetics

    Protect your brand by verifying critical product information on every package This short webinar guides you through the various applications for vision inspection to help you choose the right solutio...
  • Automating the Pharma Pipeline

    This webinar is aimed at chemists and engineers engaged in pharmaceutical and high-value chemical development. It outlines how to increase productivity and obtain more information from experiments by...


  • Live Webinar: European Pharmacopoeia "Balances for Analytical Purposes"

    Compliance with Ph. EUR. General Chapter 2.1.7 This is a live webinar about the new Ph. EUR. General Chapter 2.1.7. As of January 1, 2022, the European Pharmacopoeia is a legally binding reference for the quality control of medicines. In this webinar you will learn everything about the new Ph. EUR. General Chapter 2.1.7 Balances for Analytical Purposes. As of January 1, 2022, the European Pharmacopoeia is a legally binding reference for the qua...
  • Online Seminar: PAT for Oligonucleotide and Peptide Synthesis

    Ensure Your Yield, Purity and Cost Objectives Are Met - March 30, 2022 Learn how industry experts leverage data-rich experimentation, enabled by Process Analytical Technology (PAT), to ensure yield, ...
  • How to Select the Correct Metal Detection System

    Exploring Benefits for Brand Protection, OEE, Compliance and Lowering Total Cost of Ownership This on-demand webinar explores how to choose the right metal detection system to invest in and why it is...
  • On-Demand Webinar: Advanced - Weighing in Hazardous Areas

    A Focus on Dust This advanced webinar takes a look at hazardous area weighing: 1st Module A focus on the risk of dust 2nd Module the advantages of intrinsically safe design 3rd Module new develo...