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Process Automation Articles & Analysis
30 articles found
Quality issues in medical devices often point to underlying weaknesses in the system, and ISO 13485-compliant CAPA is essential for correctly identifying cause and preventing the problem from recurring. Here’s an overview of CAPA requirements in ISO 13485 for medical device ...
For biologics such as monoclonal antibodies, recombinant proteins, and viral vectors, downstream processing can account for the majority of production costs, making process optimization both a scientific challenge and a commercial necessity. ...
Whether it is medical research or drug manufacturing, tablet press is a vital link. Let's see how to choose the one that suits you best.Grand pack.The field of drug delivery is constantly evolving, driven by the core goal of improving therapeutic outcomes—enhancing efficacy, reducing toxicity, boosting patient compliance, and even enabling entirely new medical treatments. The global drug delivery ...
A nurse works late, spending hours manually logging incident reports instead of caring for patients. A hospital administrator wrestling with scattered spreadsheets, trying to prepare for an audit that’s days away. Sound familiar? These time traps can be difficult to avoid in private healthcare. However, every minute lost to administrative inefficiencies is valuable time lost for ...
Here are the key reasons why: Efficiency and Automation: RFID eliminates manual processes, reducing human error and speeding up operations. Enhanced Security: RFID tags help prevent theft, loss, and unauthorized access, ensuring asset safety. Cost Savings: By automating inventory and asset tracking, businesses save time and resources. ...
Overview Cleanrooms are essential in the pharmaceutical industry, providing controlled environments for the aseptic production of sterile products. Recently, big data analytics has emerged as a transformative tool, offering new ways to enhance cleanroom performance beyond traditional ...
Benefits of Automated Pharmaceutical Packaging Solutions Automation in pharmaceutical packaging involves the use of machines and software to streamline the packaging process. When implemented correctly, automation can bring many benefits to your pharmacy. Higher Accuracy on Inspections Automated pharmaceutical ...
The cryogenic process is a method of freezing and storing samples that involves cooling the temperature of biological materials to stop normal cellular processes and prevent sample degradation for long-term storage. The cryogenic process and cryo storage are ideal solutions for the storage of biological samples and ensuring cell viability over ...
A more efficient way to prepare samples for IC analysis is by using Metrohm Inline Sample Preparation (MISP) techniques to automate the process. Either Metrohm Inline Ultrafiltration (UF) or Inline Dialysis can be used to safeguard the IC system from harmful matrix components while simultaneously reducing manual labor and increasing sample ...
ByB&W Tek
Scientists continuously face pressure to purify biologics like protein therapeutics with maximum yield while minimizing cost and developing processes as quickly as possible. Downstream processing often accounts for more than half the cost of goods overall and significantly impacts manufacturing timelines. Affinity chromatography manages to achieve high ...
Come and see an automated biologics processing unit in operation at a one-day Symposium “Integrated Process Strategies For Regional Biopharmaceutical Supply” on March 28, 2023, Sedgefield, UK. ...
Pharmaceutical distributors take advantage of the distribution of new medicines to pharmacies to collect this waste and deposit it in authorized managers who take it to the packaging and drug waste sorting plant, located in Tudela de Duero (Valladolid), a pioneering facility worldwide where pharmaceutical and health waste goes through different phases to separate the containers and the remains of ...
This traditional process is not only time consuming; it can result in human error and a reduction in quality of your annotations. If you find this is the case for your current process, why not consider automating annotated CRFs to make the job a little easier? The benefits of automating annotated CRFs: They’re ...
ByFormedix
. * Whole transcriptome analysis: genes related to proliferation were up-regulated and genes related to the regulation of immune system processes (e.g., MUC1, MUC5B), inflammatory response-related genes (e.g., IL1LR1, GPX4, ADCY5) and extracellular matrix tissue-related genes (LAMB3, MMP1) were down-regulated, suggesting that CD133+ hBECs may have greater regenerative capacity. * ...
Summary OTraces in collaboration with the Gertsen Institute in Moscow performed a blinded validation study on OTraces breast cancer detection products, the CDx Chemistry System for processing automated tests for detection of cancer; BC Sera Dx Immunochemistry test kit for the measurements of proteins that are predictive as a group of the presence on breast cancer ...
Situation When the Covid-19 pandemic began, businesses large and small had to move quickly to protect their workforce. By April 2020, widespread government mandates and regulations were put in place for companies to remain operational. The first hurdle for businesses was the sudden need for logging employee temperatures, symptoms, travel to hotspots, Covid-19 exposure, and communicating mask ...
ByRedlist
Automation now eases manual processes in so many aspects of society, from smart home switches to manufacturing lines. ...
The pressure on clinical laboratories has increased significantly in recent years and the need for fast, accurate and thorough data is reaching unprecedented levels. COVID-19 has put an intense spotlight on automated liquid handling systems in particular, and with worldwide reliance and investment in PCR testing capabilities, this insatiable demand for rapid testing is unlikely to dissipate soon. ...
Since baby elephants are still in the growing process, it's impossible to estimate the impact of eating a particular fruit on their trunk's length. ...
It is an end result of a lengthy, multi-step process that includes material, time and financial investment—not only in research and development, design, and manufacturing, but the entire process of verification and validation, regulatory approval, and market placement that comprises each stage of the product life-cycle. ...