MMR Consulting
MMR Consulting is a life‑sciences and regulated‑industries consulting firm offering engineering, commissioning/qualification/validation (CQV), automation and control systems design, computer system validation, GMP compliance, project management and digital/paperless validation services. The firm provides end‑to‑end project support from feasibility and design through commissioning, qualification and handover, and is ISO 9001 certified (QMS).
Industries
Nr. of Employees
medium (51-250)
MMR Consulting
Orland Park, Illinois, United States, North America
Products
Commissioning, Qualification and Validation (CQV) Services
Provides end-to-end CQV services including equipment, facilities, automation, and process validation to ensure compliance with industry regulations.
Automation Services
Delivers design, development, and validation of process and utilities automation systems for life sciences manufacturing environments.
Project Management & Project Controls
Manages complex capital programs and project controls tailored to the life sciences industry to ensure project delivery.
Computer System Validation (CSV)
Provides risk-based validation of computerized systems including ERP, LIMS, MES, and process control software to ensure regulatory compliance.
Kneat Paperless Validation Services
Implements and supports KneatGx™ software for digital validation management, including managed services and training.
Engineering Services
Offers multi-disciplinary engineering including bioprocess, clean utilities, equipment, and mechanical & electrical utilities engineering for life sciences projects.
Commissioning, Qualification and Validation (CQV) Services
Provides end-to-end CQV services including equipment, facilities, automation, and process validation to ensure compliance with industry regulations.
Automation Services
Delivers design, development, and validation of process and utilities automation systems for life sciences manufacturing environments.
Project Management & Project Controls
Manages complex capital programs and project controls tailored to the life sciences industry to ensure project delivery.
Computer System Validation (CSV)
Provides risk-based validation of computerized systems including ERP, LIMS, MES, and process control software to ensure regulatory compliance.
Kneat Paperless Validation Services
Implements and supports KneatGx™ software for digital validation management, including managed services and training.
Engineering Services
Offers multi-disciplinary engineering including bioprocess, clean utilities, equipment, and mechanical & electrical utilities engineering for life sciences projects.
Services
End‑to‑end CQV services including CQV planning, procedures/templates, equipment and utility qualification, automation systems qualification, cleaning/process/thermal validation and C&Q project management.
Risk‑based CSV for cloud and on‑premises systems (ERP, LIMS, MES, eQMS, process control systems) including SOP development, validation deliverables, templates and program implementation.
Process and utilities automation design, control strategy development, application development, integration, commissioning and automation validation for PLC/DCS/SCADA, historian and BAS systems.
Full project management and project controls offerings including outsourced PMO, project documentation, stage‑gate deliverables, cost/schedule control, risk management and construction management.
Implementation, configuration, training and managed hosting of paperless validation platforms, plus provision of certified program packs and template management as a managed service.
Multi‑disciplinary engineering including process design, equipment engineering, critical utilities and specialized systems for biologics, pharmaceuticals, cosmetics and related industries. Services limited to select jurisdictions for design delivery.
End‑to‑end CQV services including CQV planning, procedures/templates, equipment and utility qualification, automation systems qualification, cleaning/process/thermal validation and C&Q project management.
Risk‑based CSV for cloud and on‑premises systems (ERP, LIMS, MES, eQMS, process control systems) including SOP development, validation deliverables, templates and program implementation.
Process and utilities automation design, control strategy development, application development, integration, commissioning and automation validation for PLC/DCS/SCADA, historian and BAS systems.
Full project management and project controls offerings including outsourced PMO, project documentation, stage‑gate deliverables, cost/schedule control, risk management and construction management.
Implementation, configuration, training and managed hosting of paperless validation platforms, plus provision of certified program packs and template management as a managed service.
Multi‑disciplinary engineering including process design, equipment engineering, critical utilities and specialized systems for biologics, pharmaceuticals, cosmetics and related industries. Services limited to select jurisdictions for design delivery.
Expertise Areas
- Commissioning, qualification and validation (CQV)
- Computer system validation (CSV) and digital validation
- Process automation and control systems
- Bioprocess and pharmaceutical process engineering
Key Technologies
- Programmable Logic Controllers (PLC) programming
- Distributed Control Systems (DCS) and SCADA
- Manufacturing Execution Systems (MES)
- Process historians and visualization
News & Updates
Company is certified to ISO 9001 Quality Management System, demonstrating conformity to international QMS requirements.
Company is certified to ISO 9001 Quality Management System, demonstrating conformity to international QMS requirements.