Healthcare
PRODUCTS
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Say goodbye to paper and manual spreadsheets and hello to maximum efficiency, productivity, and visibility! Plex MES is the only single-instance, multi-tenant cloud-based SaaS production platform that operates at scale. This allows for a common production ecosystem that supports a real-time, single source of data. It can tie production and inventory to quality with end-to-end, detailed traceability. With Plex, you can connect people and systems, automate processes, track data from end to end, and capture and analyze information like never before.
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What is included in Forge's DMF?
DMFs come in all shapes and sizes, but Forge's DMF includes the following components:
- Information on our critical raw materials, including our Ignition Cells™ and pEMBR™ adenovirus helper plasmid
- An overview of our platform AAV manufacturing process
- Process controls
- Facility layout and engineering information
- And more!
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As life science companies turn to digital strategies and convert from manual paper to digital processes, they need expertise in design and implementation to ensure continuous improvement.
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At 120Water, we take the weight off the shoulders of our clients. From expert guidance and best practices to a proven activation process, we help ensure your program achieves ongoing success.
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Connect your entire operations across internal and external sites
Product Lifecycle Data
Consolidate data for each stage of a drug’s lifecycle in one place.
- Expedite compliance by centralizing product lifecycle data for each stage
- Shorten the time between one stage to the next
- Streamline tech transfer and accelerate to commercial rollout
Enterprise Recipe Management
Optimize enterprise recipe management across environments and sites.
- Create and manage a core set of enterprise-wide templates
- Get access to customizable resources for every stage
- Easily assign your templates and resources to individual sites and teams
External Manufacturing Collaboration
Ditch email and calls for automated communications.
- Grant direct view-only access and batch review options as needed
- Provide customers with a self-service approach to their sponsored batches
- Make real-time, data-driven decisions
Tech Transfer
Quickly and easily move all your master resources and data.
- Securely store batch templates, procedures, materials and equipment classes
- Easily share process knowledge and data through transferable global recipes
- Shift a product ad-hoc from one team to another
WHITE PAPERS AND CASE STUDIES
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Empowering Freenome: Large-Scale Data Quality And Compliance
Delve into the five key ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.
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DC Water's Digital Twin Solution
Explore how operational and financial resilience can be improved by implementing a water infrastructure digital twin.
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Risk Assessment As A Process Quality Assurance Tool
Discover how an effective approach to risk management can further ensure delivery of a high quality drug or medicine to the patient.
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Operational Considerations For EU Clinical Trial Readiness & Execution
Gain a comprehensive understanding of the Clinical Trial Regulation (EU) 536/2014 (CTR), which has equipped stakeholders to navigate the altered regulatory landscape and prepare for conducting clinical trials in the EU/EEA.
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Control Your Data Flow, Control Your Trial
The surge of healthcare data threatens to cripple healthcare organizations. But an effective data flow environment can get it under control.
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Leveraging AMI For The Low Voltage Landscape
In this white paper, explore ways that utilities are prioritizing grid management use cases and challenges that utilities face in capturing the full value of AMI data.
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Navigating The Privacy Tightrope For CTIS
Examine the challenges, potential risks, recommended best practices, and future trends related to anonymizing personal data for Clinical Trials Information System submissions.
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Busting The Top 7 Data Quality Myths In Clinical Trials
Separate fact from fiction and dispel the myths about evolving clinical data collection, monitoring, and reporting by diving into this analysis of technology use in clinical trials.
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The Need For Direct RF In An Evolving Defense Environment
Discover why it is important to move toward direct RF, explore its capabilities and applications, and see how innovative products can help make the DoD’s vision a reality.
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Critical Cleaning For 3D Printing In The Life Sciences
Here, we focus on the critical cleaning of hard surfaces utilized in 3D printing processes across industries, such as extruded plastics, photosensitive substrates, metals, and metal alloys.
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Increase Production Capacity With Virtualized Process Automation
Learn how Sleeman Breweries grew their production, improved process control, and avoided the high expense of building a new greenfield facility.
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How To Save 9k Hours And Cut Deviations By 27%
This pharma company transitioned off paper, slashing their deviation count and saving thousands in onsite hours. Learn how they were able to streamline business operations and free up resources.
NEWS
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MadCap Software Acquires Xyleme To Expand Suite Of Intelligent Content Management Products1/11/2024
MadCap Software, Inc., the leader in multi-channel content authoring, management and publishing, backed by global investment firm Battery Ventures, today announced the acquisition of Xyleme, Inc., a leader in intelligent content management for the development, management, delivery, and syndication of vital proprietary learning and development (L&D) content across the enterprise.
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Dynacare Acquires Valley Medical Laboratories4/19/2023
Dynacare, a Labcorp subsidiary and one of Canada’s leading health and wellness solutions providers, today announced that they have entered into an agreement to acquire Valley Medical Laboratories in British Columbia effective May 1, 2023.
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ProPharma Launches An Integrated MedTech Organization Providing End-To-End Solutions For Innovators11/16/2023
ProPharma Group, the world’s largest Research Consulting Organization (RCO) and the leading global provider of regulatory, clinical and quality compliance services for the life sciences industry, has today launched a new Integrated Global MedTech Practice to provide end-to-end solutions for medical technology companies.
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FDA, Industry Actions End Sales Of PFAS Used In US Food Packaging2/28/2024
Today, the U.S. Food and Drug Administration is announcing that grease-proofing materials containing per- and polyfluoroalkyl substances (PFAS) are no longer being sold for use in food packaging in the U.S.
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Syneos Health Partners With Equicare, Optimizing Data Capture And Integration To Accelerate Clinical Trial Research2/8/2023
Syneos Health® (Nasdaq:SYNH), the only fully integrated biopharmaceutical solutions organization, today announced a strategic partnership with Equicare to use proXimity™, an innovative cloud-based software platform that accelerates the transfer of clinical trial subject data from multiple electronic health records (EHR) to the sponsor’s electronic data capture systems (EDC).