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
Carlsbad, California, United States
Products
Kneat Paperless Validation Services
Full range of services including Managed Service, Kneat Go, and Kneat Gx implementation, scaling, and workspace operation.
KneatGx
A feature rich paperless validation platform purpose built for the Life Sciences, digitizing the entire validation life-cycle in a 21 CFR Part 11 compliant web-based software.
Commissioning, Qualification and Validation (CQV) Services
Commissioning & Qualification expertise for a variety of cGMP and cGLP process, equipment and facility systems.
Computer System Validation
Custom risk-based approach to Computer System Validation (CSV) including deliverables for ERP, LIMS, eQMS, MES, BAS, PSC, and DCS systems.
Automation Services
Integrated automation and information solutions to achieve greater efficiencies, lower life-cycle costs, and maintain product quality.
Project Management & Project Controls
Management of complex capital programs and project controls tailored for the Life Sciences industry.
Kneat Paperless Validation Services
Full range of services including Managed Service, Kneat Go, and Kneat Gx implementation, scaling, and workspace operation.
KneatGx
A feature rich paperless validation platform purpose built for the Life Sciences, digitizing the entire validation life-cycle in a 21 CFR Part 11 compliant web-based software.
Commissioning, Qualification and Validation (CQV) Services
Commissioning & Qualification expertise for a variety of cGMP and cGLP process, equipment and facility systems.
Computer System Validation
Custom risk-based approach to Computer System Validation (CSV) including deliverables for ERP, LIMS, eQMS, MES, BAS, PSC, and DCS systems.
Automation Services
Integrated automation and information solutions to achieve greater efficiencies, lower life-cycle costs, and maintain product quality.
Project Management & Project Controls
Management of complex capital programs and project controls tailored for the Life Sciences industry.
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.