Focus Piece: Risk Based Utility Monitoring

In the era of big data, regulations are evolving to encourage data analytics. Trending capabilities, preventative actions and process improvement are essential for a complete contamination strategy. Learn now Novatek’s Utility Monitoring Management Software can help you best manage your utilities during pharmaceutical manufacturing. Learn now Novatek’s Utility Monitoring Management Software can help you best…

Case Study: SANOFI GENZYME Digitizes Environmental & Utility Monitoring Data with Novatek

Novatek International provided Sanofi Genzyme’s Lyon, France pharmaceutical manufacturing site an industry-focused digital solution to improve their contamination control in data integrity, automating trend analysis, and reduced workloads. After a successful 12-week implementation, the number of samples taken, protocols created, and specification created was extraordinary. “The project is a success, the QC department of Sanofi…

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KENX Virtual Training: Pharmaceutical Water Systems

Pharmaceutical Water Systems Virtual Training Hosted by KENX Water is perhaps the biggest critical utility used in pharmaceutical manufacturing and yet, perhaps the most overlooked in terms of understanding, compliance, development, and validation. This one-day virtual training takes a deep dive into the design, validation, testing, and control of water systems. In addition to receiving…

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WEBINAR: Got 15 min? Quick & Straight to the Facts

In response to COVID-19, both Novatek’s Environmental Monitoring Software and NEW Disease Control & Hygiene System are advanced analytical, and data driven technologies that supports effective quality control and reduces risk. Join us as we launch our 15 Minute Webinar Series to deliver quick and “straight to the facts” demonstrations on how to reduce your…

Risk Based Environmental Monitoring & Efficiencies Gained With Use of an Automated System – An Industry Roundtable Discussion

The Southern California Discussion Group of the ASQ Biomedical Division Presents: Risk Based Environmental Monitoring (EM): How to use risk to ensure your EM Program is value added & efficient An Industry Roundtable Discussion Non-viable air, viable air, and surface monitoring of controlled environments is not a new concept and has been a regulatory requirement…

Novatek International Travels to Indonesia November 2012

Novatek International is very proud to announce that Mr. Parsa Famili, CEO and President of Novatek International was the keynote speaker of the Pharmaceuticals Executive Meeting and Discussions in Jakarta, Indonesia. During this meeting scientific processes of Indonesian Pharmaceutical companies and Novatek solutions were discussed. Novatek routinely participate in high level scientific and corporate discussions…

PDA/FDA Joint Regulatory Conference – Booth 21

September 10-12 – Baltimore, MD Novatek International will be exhibiting its process-based LIMS software solutions such as Quality Management Systems, Stability Program Management, Environmental Monitoring & Utility Monitoring, Calibration & Preventive Maintenance, and, Automated Packaging Component Proof Reader at the 2012 PDA FDA Joint Regulatory Conference in Baltimore, MD USA. Come visit us at Booth…