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OVERVIEW | APPROACH | COMPETENCIES | EXPERIENCE | LITERATURE
DME Alliance has provided over ten years of dedicated service to the life sciences industry. Team experience includes R&D facilities, pilot plants, preclinical manufacturing, and GMP production facilities (primary and secondary manufacturing). The combination of advanced project delivery methodologies with in-house process expertise establishes DME Alliance as the supplier of choice for the turnkey delivery of expansion, renovation and remediation projects in biotechnology and pharmaceutical facilities.
DME Alliance has knowledgable and competent subject matter experts in process science and equipment design. Projects typically include mission-critical process operations requiring an in-depth understanding of GMP compliance, contamination control, cleaning & sterilization requirements, process containment, clean utilities and process automation. DME offers turnkey solutions encompassing concept through detailed design, procurement, construction, commissioning, validation, operation and maintenance.
OVERVIEW | APPROACH | COMPETENCIES | EXPERIENCE | LITERATURE
The design and delivery of biotech and pharmaceutical process facilities requires a project approach in which the process mission is central and pervasive. This is why DME Alliance has made it a priority to develop expertise in the applied process technologies that are essential for the success of these facilities. DME leverages in-house process knowledge and experience to efficiently identify key user requirements and prioritize tasks. This allows fast-track execution of tech-heavy projects without sacrificing quality. DME's approach to project execution is process driven and risk-based. This enables turnkey solutions that deliver best value by focusing premium resources on essential process requirements, and by preserving GMP design intent throughout the entire project life cycle.
OVERVIEW | APPROACH | COMPETENCIES | EXPERIENCE | LITERATURE
DME Alliance core competencies are uniquely suited to process facilities in the regulated life sciences sector.
Pharma & Biotech Process Science
cGMP Equipment Design
Mechanical Design; CADD
SIP & CIP Engineering
Aseptic Design & Containment
Disposables and Single-Use Technology
Regulatory Compliance
Failure Analysis & Process Remediation
Facility Maintenance Programs & Procedures
Project & Program Management
Construction and Verification practice for GMP Facilities
OVERVIEW | APPROACH | COMPETENCIES | EXPERIENCE | LITERATURE
DME Alliance has experience and expertise in biopharm unit operations.
Process Reactors, Cell Culture & Fermentation
Perfusion, Recovery & Cell Disruption Systems
MF/UF & Depth Filtration
Centrifugation & Chromatography
Extraction, Crystallization, Distillation
Formulation, Dryers & Lyophilization
Compounding & Fill/Finish
Solution Preparation, Buffer & Media Systems
Sterile Processing, CIP & SIP Systems
GMP Autoclaves & Glasswashers
Clean Utilities & Biowaste Inactivation
OVERVIEW | APPROACH | COMPETENCIES | EXPERIENCE | LITERATURE
Download DME Alliance literature in PDF format by clicking on the links below.
SERVICE GUIDES
SECTOR SOLUTIONS
DME Alliance Inc.
...where Process Science meets Engineering Excellence.
Tel 877.842.7123
©2004 by DME Alliance Inc. All rights reserved. Read our privacy statement. Some photos in this web site used with permission courtesy of B. Braun Biotech, JV NorthWest, and Lee Industries. Web site design by Down to Earth Web Design
