OQ

OQ Chemicals Launches Oxlube L7-NPG Ester Base Oil for EV Fluids

Retrieved on: 
Thursday, September 1, 2022
Chemicals, Plastics, Automotive, Other Automotive, EV, Electric Vehicles, Manufacturing, Other Manufacturing, Organic acid, Oxo, Oil, Alcohol, Maintenance, Plastic, Viscosity, Lubricant, OQ, Trimethylolpropane, EV, TMP, Amine, Efficiency, Synthetic oil

The global chemical company OQ Chemicals introduces its new ester base oil Oxlube L7NPG, specifically developed to help improve the performance and efficiency of electric vehicles (EV).

Key Points: 
  • The global chemical company OQ Chemicals introduces its new ester base oil Oxlube L7NPG, specifically developed to help improve the performance and efficiency of electric vehicles (EV).
  • OQ Chemicals will launch Oxlube L7-NPG at the Lubricant Expo in Essen, Germany, from Sept. 6-8, 2022.
  • Especially its low viscosity and high flash point make Oxlube L7-NPG ideally suited for energy-efficient EV fluids, stated Svea Meuser, Global Marketing Director Acids at OQ Chemicals.
  • Oxlube L7-NPG complements Oxlube L9-TMP, which is used as a co-solvent ester in engine oils as a drop-in replacement for the conventional C8/C10 acid-based TMP (Trimethylolpropane) ester.

Pharmaceutical Analytical Method Validation, Verification and Transfer Course (October 6-7, 2022) - ResearchAndMarkets.com

Retrieved on: 
Wednesday, August 24, 2022
Health, Pharmaceutical, Transfer, Percussion section, ICH, The Compendious Book on Calculation by Completion and Balancing, DQ, IQ, Safety, OQ, Drug development, USP, Informal Methods (Validation and Verification), PQ, Medical device

The "Analytical Method Validation, Verification and Transfer" training has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Analytical Method Validation, Verification and Transfer" training has been added to ResearchAndMarkets.com's offering.
  • The factors to consider for verification of the compendial procedures will also be discussed.
  • In addition, different approaches for the transfer of analytical procedure from one lab (transferring) to other lab(s) (receiving) under different circumstances will be covered.
  • Reliable analytical results are necessary to make informed decision about the quality and safety of the products in the pharmaceutical industry.

3 Day Computer System Validation (CSV) Training Program (September 21-23, 2022) - ResearchAndMarkets.com

Retrieved on: 
Tuesday, August 9, 2022
Education, Technology, Training, Other Technology, Cloud, FDA, CSV, Matrix, PQ, Industry, Technology, Immersion, Algebraic group, Method, OQ, Title 21 CFR Part 11, Requirement, COTS, Validation, IQ, Risk management, Medical device

The "Computer System Validation (CSV) Training" training has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Computer System Validation (CSV) Training" training has been added to ResearchAndMarkets.com's offering.
  • This computer system validation course is designed to completely immerse you in the principles, methods, and best practices of Computer System Validation (CSV).
  • You will learn about the regulations that impact your systems and gain hands-on practice writing validation documents.
  • Many exercises on Validation Plan, the Requirements Traceability Matrix, and the Validation Summary Report.

reduce: OQ Chemicals Switches to Green Power and Cuts CO2 Emissions

Retrieved on: 
Tuesday, August 2, 2022
Chemicals, Plastics, Environment, Manufacturing, Sustainability, Alternative Energy, Green Technology, Energy, Goal, Steam, OQ, Oxo, Electricity, Climate, Allen County, Indiana, Alcohol, Monheim am Rhein, Plastic, Lubricant, Amine, Organic acid, Heat, Natural gas, Renewable energy

Its locations in Monheim am Rhein, in Houston, Texas, and the Dutch production site in Amsterdam already use 100 percent green power.

Key Points: 
  • Its locations in Monheim am Rhein, in Houston, Texas, and the Dutch production site in Amsterdam already use 100 percent green power.
  • At its other sites in Germany and the USA, OQ Chemicals will initially use green power certificates (Energy Attribute Certificates - EACs) during a transitional phase.
  • In the medium term, the company intends to use only green power at all its locations worldwide.
  • Achieving climate neutrality will be one of the most important goals for OQ Chemicals in the coming years, commented OQ Chemicals CEO, Dr. Oliver Borgmeier.

New Methyl Methacrylate Plant in Bay City, Texas: OQ Chemicals Signs Final Investment Decision

Retrieved on: 
Tuesday, July 26, 2022
Utilities, Construction & Property, Other Manufacturing, Energy, Engineering, Chemicals, Plastics, Other Construction & Property, Manufacturing, MMA, View, Advent International, OQ, CEO, Oxo, Alcohol, Lima, Amine, Technology, Organic acid, PMMA, Engineering, FID, Petrochemical

Global chemical manufacturer OQ Chemicals signed a final investment decision (FID) to build additional capacity of propionic aldehyde as well as infrastructure.

Key Points: 
  • Global chemical manufacturer OQ Chemicals signed a final investment decision (FID) to build additional capacity of propionic aldehyde as well as infrastructure.
  • This is to support Rhm, one of the leading methacrylate producers, in constructing a world-scale methyl methacrylate (MMA) plant at an OQ Chemicals production site.
  • OQ Chemicals will integrate the plant into its production site at Bay City, Texas, and provide raw materials, utilities, and site services to Rhm.
  • At OQ Chemicals, we are looking forward to welcoming Rhm to our site in Bay City.

Verification and Validation - Product, Equipment/Process, Software and QMS (January 18-19, 2022) - ResearchAndMarkets.com

Retrieved on: 
Wednesday, July 20, 2022
Manufacturing, Engineering, Intelligence quotient, DQS, V&V, EU, Electronic, OQ, QMS, Software, PQS, Title 21 CFR Part 11, FDA, Veni, vidi, vici, MDD, Medical device, Risk management

Quality Management System - 21 CFR 11, Electronic Records/Signatures;

Key Points: 
  • Quality Management System - 21 CFR 11, Electronic Records/Signatures;
    The roles of different V&V protocols;
    How to employ equipment/process DQs, IQs, OQs, and PQs, or their equivalents,
    V&V against a background of limited company resources;
    The FDA's 11-element software matrix simplifies "as-product", in-product", process and equipment, et al, software VT&V;
    Assure key U.S.FDA and comparable EU MDD/ISO requirements are not overlooked;
    The QMS and 21 CFR Part 11, "Electronic Records/Signatures" V&V;
    Hands-on examples and activities show real-world implementation of useful principles, tools and templates;
    Develop a "Working Definition" of V&V, Qualification, and related terms
    How to document a "risk-based" rationale, and use it in a resource-constrained environment
    Determine key "milestones" and "tasks" in a project; device sample provided

Nuvolo Releases Fully Validated Multi-Tenant Offering for Life Sciences Companies

Retrieved on: 
Thursday, July 7, 2022
Documentation, CEO, IWMS, OQ, Validity (statistics), Industry, GxP, Public sector, Technology, List of life sciences, GameChanger, Software, General manager, Integrated workplace management system, PQ, Construction, Nuvolo

PARAMUS, N.J., July 7, 2022 /PRNewswire/ -- Nuvolo, the leader in modern workplace management solutions, announced today that its multi-tenant offering of Connected Workplace for Life Sciences is now fully validated for use in GxP environments.

Key Points: 
  • PARAMUS, N.J., July 7, 2022 /PRNewswire/ -- Nuvolo, the leader in modern workplace management solutions, announced today that its multi-tenant offering of Connected Workplace for Life Sciences is now fully validated for use in GxP environments.
  • Nuvolo fully validated its software to provide smaller, early-stage biotech, medical device and diagnostic companies with a compliant system for tracking their regulated assets without excessive financial overhead.
  • "Life sciences is a strategic industry for Nuvolo and we are developing capabilities, features and products focused on the unique requirements of this industry," said Ethan Smith, General Manager, Life Sciences, at Nuvolo.
  • "Providing a fully validated, multi-tenant IWMS for life sciences is a gamechanger that takes all the possibilities of cloud technology to a new level.

Medical Device Software and Cybersecurity Courses - 5 Webinar Bundle - ResearchAndMarkets.com

Retrieved on: 
Monday, June 13, 2022
Security, Medical Devices, Health, Technology, Software, OQ, PQ, Software, CAD, Lists of TVB dramas and series, CAM, PQS (software), DQ, IQ, Medical device

Software used in process validation (such as statistical calculation software, spreadsheets, etc.).

Key Points: 
  • Software used in process validation (such as statistical calculation software, spreadsheets, etc.).
  • Software used in design and development processes (such as CAD software, CAM software, software development tools, software test tools, compilers, editors, code generators, etc.).
  • Software used to automate part of the quality process (such as complaint-handling systems, lot-tracking systems, training-database systems, etc.).
  • Software used to create, transmit, modify, or store electronic records that are required by regulation.

2 Day Virtual FDA and EU Process Validation and Equipment Qualification Training Course, October 20-21, 2022 - ResearchAndMarkets.com

Retrieved on: 
Monday, June 13, 2022
FDA, Machine Tools, Metalworking & Metallurgy, Health, Manufacturing, Validation master plan, OQ, FDA, PQ, QSR, Maintenance, VMP, Calibration, IQ, Locksmithing, Medical device, EU

The "FDA and EU Process Validation and Equipment Qualification Training Course" training has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "FDA and EU Process Validation and Equipment Qualification Training Course" training has been added to ResearchAndMarkets.com's offering.
  • And that includes any ancillary equipment that affects production, such as environmental systems and contamination controls.
  • This training program will list the documents required for equipment qualification and process validation and discuss how to manage documents appropriately.
  • The course will also discuss best practices for writing and executing sound protocols for equipment qualification (IQ, OQ, PQ) and process validation.

On Course for Growth: OQ Chemicals Strengthens Leadership Team With Dr. Albrecht Schwerin as New COO

Retrieved on: 
Thursday, June 9, 2022
Oil, Gas, Manufacturing, Energy, Environment, Chemicals, Plastics, Chemistry, GEMBA, Chemical industry, Lubricant, Knowledge, Development, COO, Henkel, Institute of technology, IESE Business School, Business administration, OQ, Organic acid, Alcohol, Amine, Plastic, Management, Global

Global chemical manufacturer OQ Chemicals is further expanding its management team: Effective immediately, Dr. Albrecht Schwerin will be responsible for operations as the new Chief Operating Officer (COO).

Key Points: 
  • Global chemical manufacturer OQ Chemicals is further expanding its management team: Effective immediately, Dr. Albrecht Schwerin will be responsible for operations as the new Chief Operating Officer (COO).
  • With his extensive knowledge and experience in the chemical industry, Dr. Schwerin will significantly contribute to strengthening OQ Chemicals and its global production sites.
  • His core responsibilities include strategic transformation programs and the sustainability initiative "reduce", with which OQ Chemicals is striving for climate neutrality.
  • "We are very pleased to welcome Dr. Albrecht Schwerin to the OQ Chemicals management team.