Regulatory Compliance Videos

  1. Package Integrity Testing Of Dry-Fill Flexible Packaging With VeriPac FLEX 11/16/2021

    The VeriPac FLEX Systems are available in several configurations to accommodate various package specifications. Each model achieves a specific range of test sensitivity and various test chamber sizes are available depending upon the package size and characteristics.

  2. Micro Leak Detection Of Syringes, Vials And Liquid Filled Packaging With The VeriPac 455 11/16/2021

    VeriPac 455 is a non-destructive inspection system for highly sensitive micro leak detection of empty & pre-filled syringes, liquid filled & lyophilized vials and other liquid filled packaging. The VeriPac 455 inspection technology that can be incorporated into protocols at any point in the handling process as it is non-destructive, non-invasive and requires no sample preparation. 

  3. Seal-Sensor Technology For In-Line Pouch Seal Inspection 11/16/2021

    PTI is integrating the latest technologies for inspecting pouch seals utilizing a method that inspects and analyzes pouch seals non-destructively. Seal-Scan and Seal-Sensor utilize Airborne Ultrasonic Technology (ABUS) that inspects and analyzes pouch seals non-destructively.

  4. Life Sciences Quality And Compliance Software Product Demonstration 8/30/2021

    MasterControl Inc. is a leading provider of cloud-based quality and compliance software for life sciences and other regulated industries. The MasterControl Platform helps organizations digitize, automate, and connect quality and compliance processes across the regulated product development life cycle.

  5. We Are Asymchem 8/30/2021

    We're a CDMO that researches the possibilities, develops new technologies, and applies new processes in a continual drive toward optimization.

  6. Aseptic Vial Filling 6/18/2021

    We offer a unique range of formulation and aseptic filling in vials, prefilled syringes or cartridges to address production needs that span from small early stage clinical products to larger scale commercial products.

  7. Using Egnyte For Life Sciences As GxP Repository 1/6/2021

    Transitioning from the research phase to the clinical trial phase is a big step for any company, but it also means challenges, not the least of which means your electronic records need to comply with FDA 21 CFR Part 11 and GxP. In this democast, we will review how to deploy and use a GxP-compliant repository using Egnyte’s industry-focused platform, Egnyte for Life Sciences, without sacrificing usability or security, and without creating administrative overhead.

  8. Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing 1/4/2021

    The Faciliflex Module is a transformational new concept in designing cleanrooms for the production of lifesaving therapeutics.

  9. Your Contract Manufacturer Partner 12/14/2020

    Discover an integrated solution for pharmaceutical companies that offers a broad range of manufacturing services and capabilities to produce high-quality devices.

  10. GxP Audit Trails For FDA Compliance 12/8/2020

    Many companies struggle with ensuring a strong compliance envelope as they transition from an R&D culture to a more-structured, regulated one. In this video we will cover Egnyte for Life Sciences platform overview focusing on audit trails, versioning, and reporting capabilities that can help you overcome your compliance challenges.