Be sure to check back frequently for news, events, resources and videos relevant to the pharma industry!

News

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    Remote FDA Inspection

    Article
    Increasing Demands of a Digitized World While the Covid-19 pandemic has delivered challenges across the board when it comes to the production of pharmaceutical goods (among other things), it has also thrown governmental programs into disarray. Nowhere is this more clear than in the FDA's own failure to implement a solution for conducting remote inspections, which has drawn sharp criticism from the pharmaceutical industry. At issue is the fact th...
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    How Brexit Impacts the Pharma Industry

    Article
    The pharmaceutical industry is one of the most regulated industries in the world. When it comes to international trade, Mutual Recognition Agreements ensure the international harmonization of complia...
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    Three Major Trends That Impact the Pharmaceutical Industry

    Article
    The pharmaceutical industry is in a state of flux. Even if the Covid-19 pandemic is not the trigger, it has played its part in how the industry will evolve going forward. In this article, we highligh...
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    What the Pharmaceutical Industry Can Expect From 2021

    Article
    2020 has been a year full of uncertainty, restrictions, and rapidly changing conditions. The search for a Covid-19 vaccine has kept the pharmaceutical industry busy. But even though a vaccine has now...

Downloads

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    Downstream Processing in Biopharma

    Guide
    Ensuring the Yield, Safety and Quality of Large Molecule Therapeutics Biopharmaceutical downstream processing (DSP) refers to the isolation, purification and concentration of a previously synthesized drug substance or other product from a complex bulk matrix – e.g. animal or bacterial cells – once cell growth and expansion are complete. It is typically used in mAb or protein processes, as well as in the manufacture of oligonucleotides, polysacch...
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    Tips and Tricks for Weighing on a Microbalance

    Guide
    A 10-Step Guide to Accurate Micro-weighing Getting it right first time while working safely is essential in any analytical process, but particularly when using precious samples that are only availabl...
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    OEE and Product Inspection Equipment in Pharma

    White Paper
    Focusing on Overall Equipment Effectiveness helps improve process efficiency Calculating the Overall Equipment Effectiveness is an important tool for manufacturers who wish to find ways to improve th...
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    Dissolved CO₂ Measurement In Bioreactors

    Guide
    Learn the theory of dissolved CO₂ measurement CO2 is an important metabolic indicator in bioprocessing applications. It impacts extracellular and intracellular pH and can directly and indirectly impa...

Videos

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    Pharmacopeia Regulations for Pharma Waters

    Webinar
    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 updates to pharmacopeia regulations and their application in pharmaceutical companies. The goal of this webinar is to update you on current pharmacopeia water quality requirements and regulations to help you meet your compliance needs. The 1-hour se...
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    Vision Inspection for Quality Assurance in Cosmetics

    Webinar
    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...
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    Automating the Pharma Pipeline

    Webinar
    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...
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    Good Pipetting Practice – Your Route to Excellent Data

    Webinar
    Pipettes are ubiquitous in the laboratory, playing a crucial role in all types of liquid handling processes. Accurate and precise pipetting is key to obtain high quality, reproducible results, and ca...

Events

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    21 CFR Part 11 Compliant Instruments

    Webinar
    21 CFR Part 11 is a regulation that defines the criteria for ensuring trustworthy and reliable electronic records and electronic signatures in computerized systems of FDA regulated pharmaceutical industries. It is only meaningful for instruments connected to a computer and using software. Several companies from the pharmaceutical industry have recently asked for 21 CFR Part 11 certification for instruments not connected to a PC, just using the ...
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    Live-Webinar: Lean Laboratory Principles

    Webinar
    Learn the basic principles of the original Lean idea and know the tools for systematically improving the efficiency of your workflows. A lean laboratory can be achieved by avoiding several forms of w...
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    The Flexibility of Compliance and What If …?

    Webinar
    Handling Risks and Errors in Pharma Records Handling Risks and Errors in Pharma Records - there should be procedures to stay compliant. With their focus on Data Integrity, regulation authorities are ...
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    Live Sessions: Sensor Handling and Maintenance

    Webinar
    Struggling with pH Measurements? Talk with Our Experts! Benefit from the experience of our experts and easily overcome the measurement challenges faced during your pH analysis. Learn the right set of...