Ci-DMS: IT-Compatible MES for Pharmaceutical Manufacturing
Ci-DMS has been deployed in healthcare manufacturing environments for over 30 years, supporting both global pharmaceutical organisations and smaller specialist manufacturers. During that time, it has undergone extensive IT review and approval processes across multiple sites.
The system is designed to integrate cleanly into regulated manufacturing environments without introducing unnecessary architectural complexity.
Delivering open systems for healthcare manufacturing
- We are committed to open systems and industry standards.
- CI-DMS follows the ISA guidelines.
- Our systems run on Microsoft servers using SQL Server databases.
- They work equally well from an off-site data centre or hosted locally.
ERP Integration and SAP Connectivity with Ci-DMS
- Ci-DMS is an open system and has been designed for ease of integration to ERP and manufacturing hardware, with real-time communication.
- It includes an ERP gateway, an off-the-shelf interfacing application that allows you to configure the interface to almost any ERP package.
- It also includes an interface toolbox specifically for integration to SAP ECC and S/4.
- We can provide the right level of assistance to complement your in-house skills, configuring the integration including SAP if required.
Collaborating on IT projects
- We have defined programmes for project scoping, implementation, rollout and training. This includes a generic project lifecycle to manage all of the project activities.
- We also work with you to define the process changes and start implementing them from the outset.
- The installation process is straight-forward and is also very well documented.
- Our product delivery team are experts in MES for the healthcare manufacturing sector.
- We contribute to clients’ disaster recovery planning and support DR exercises.
Supporting your GAMP 4 Validation
- Ci-DMS is classed as GAMP Category 4 (configurable software) and because it is in use at many sites is at the extreme end of this category and requires a reduced level of work to validate on-site.
- We have developed extensive documentation to support validation in your environment and offer services to supplement your in-house skills and resources if appropriate.
- Our product delivery team are all trained in computer systems validation (CSV).
MES Implementation Resources
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