Pharmaceutical Process Control and Medical Manufacturing
Rely on DMC's software and manufacturing expertise to help you with your Pharmaceutical Process Control and Medical Manufacturing. We provide engineering controls, software development, documentation, and validation solutions and services for pharmaceutical and medical companies.
Software Development
DMC has developed software and control systems for:
- Pharmaceutical Process Control
- Medical Manufacturing
- Inventory and Process Data Software Systems
- Quality Control
We employ structured Software Development Lifecycle (SDLC) methodologies to provide rock-solid, reliable solutions.
Documentation and Validation
DMC can manage and execute the entire software validation and documentation process. We have worked with the quality and validation departments of major pharmaceutical and medical companies. Our documentation experience includes:
- User Requirements Specification (URS)
- Software Requirements Specification (SRS)
- Software Design Document (SDD)
- Risk Assessment
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- Installation Qualification (IQ)
- Operational Qualification (OQ)
- Performance Qualification (PQ)
- Traceability Matrix
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We help our clients with a wide range of validations including:
- Equipment & Computer Systems Validation
- Process & Product Validation
- 21 CFR Part 11
Manufacturing Execution Systems (MES)
DMC has significant experience developing and implementing MES Solutions for the Pharmaceutical Industry.