What We Do
MMR Consulting and its dedicated team of experienced staff, are committed to delivering high quality, robust solutions for the Pharmaceutical, Biotechnology, and Life Sciences Industries. We at MMR have a passion for our people and our clients, with the majority of our staff being end-users within their industries at one time in their careers; we understand the needs of our clients.
By partnering with our clients, we surpass their needs by delivering innovative solutions within the fields of engineering, CQV activities, CSV, project management, automation services, and GMP compliance. We will see the project from feasibility to handover & technical support, while always engineering solutions with a focus on client goals and quality standards. At MMR Consulting, we are passionate about people, and experienced in engineering.
MMR’s team has shown great expertise in Clean Utilities when delivering a Global Engineering Guidance project for AbbVie on high purity water systems. Their persistence to meet timelines and deliver projects within tight schedules is also unique. MMR’s technical aptitude and project delivery was instrumental to the successful delivery of our projects, I would highly recommend MMR for Clean Utilities engineering projects.
MMR Consulting has demonstrated a profound technical knowledge in clean utilities and other process support systems / utilities, as well as a very unique project delivery model. Their creativity to figure out the real problem and determine a practical solution within a client’s constraints, as well as deliver a project within tight timelines and variable expectations, coped with their technical knowledge, engineering and commissioning skills makes them an exceptional consulting partner. I am fortunate to have worked with MMR on several projects, and would highly recommend them for either technical staff augmentation, or design and commissioning projects, with a specializing in Clean Utilities and Process.
MMR was contracted to support two high priority projects within our Toronto manufacturing facility: one focusing on chromatography skid upgrades and another on CIP process improvements.
MMR’s management of the two system upgrades was achieved in 9 months, from inception to completion. Further, the actual execution of engineering and IOQ was done during a shutdown period within 6 weeks. The CIP systems were turned over on time without impacting production.
Computer System Validation
MMR offers custom risk based approach to computer system Validation (CSV). Our CSV experts has experience in creating and executing CSV deliverables for various systems including ERP, LIMS, eQMS, MES, BAS, PCS and DCS systems, process equipment, paperless validation software, and many others.
Commissioning, Qualification and Validation Services
Full Range services from Equipment/Facilities Commissioning &Qualification, Automation Validation, to Computer System Validation, Cleaning Validation, Process Validation, Thermal/Sterilization Validation
Project Management & Project Controls
Our staff have extensive experience in managing complex capital programs and performing Project Controls tailored for the Life Sciences industry.