Quality Assurance Solutions

  1. IP Protection: A Culture Of Confidentiality 3/18/2025

    Bring your pharmaceutical product to market with peace of mind, knowing your Intellectual Property (IP) is protected by our robust CARE system.

  2. Quality Management And Compliance Consulting 4/29/2024

    Explore an extensive range of GxP services spanning CQV, Technical Consulting & Training, Quality Systems & Compliance, and Auditing for seamless project delivery and strategic support.

  3. Automated Purification For DNA, RNA, Proteins, Or Cells 6/11/2024

    Transform your laboratory processes with an automated purification instrument that delivers unmatched flexibility and performance for DNA, RNA, protein, and cell purification.

  4. Manufacturing Excellence For Life Sciences 10/19/2023

    Learn about Honeywell Manufacturing Excellence, a powerful platform built to accelerate innovation in life sciences manufacturing.

  5. Contract Manufacturing Of Devices 8/27/2021

    We offer a broad range of manufacturing services and capabilities to produce high-quality devices including pen-injectors, auto-injectors, and wearables.

  6. Corrective Action Preventive Action (CAPA) Software For Life Sciences 8/23/2021

    Quality events are inevitable, no matter how much care is taken to avoid them. As a critical part of a quality management system, CAPA identifies and addresses the root causes of high-risk quality issues and helps to limit the resulting business impact, both immediately and in the future.

  7. Should You Digitalize Your CQV Process? 8/6/2024

    Legacy paper trails are a compliance nightmare.

    Missing documents, illegible handwriting, and inconsistent data leave you scrambling and vulnerable during audits. Digital CQV captures data and objective evidence in real time, ensuring a crystal-clear audit trail with time-stamped entries and electronic signatures that meet 21 CFR Part 11 requirements.

  8. Risk Management Software For Life Sciences 8/23/2021

    Unify all risk-related activities and documents for efficient and consistent risk management.

  9. Cleaning Validation (21 CFR Part 211.67) 12/5/2008
    Alconox, Inc. can assist you in selecting an appropriate cleaner for cleaning pharmaceutical manufacturing equipment and utensils to prevent malfunctions or contamination that would alter the safety, identity, strength, quality or purity of the drug product beyond the official or other established requirements.
  10. Quality And Risk Management Software For Life Sciences 1/17/2024

    Proactively manage risks of pharmaceuticals, medical devices and other products with TrackWise Digital. The built-in templates comply with ISO 14971 and ICH Q9 allowing manufacturers to manage risks throughout the entire product lifecycle directly within TrackWise Digital.