Lucid - Industrial Automation

A Focus on Biopharma Manufacturing

GMP Documentation

Design processes follow the GMP V model, design documents are traceable from User Requirements to Detailed Design documents.

Validation and commissioning forms are traceable back to the design documentation to verify both functionality and requirements.

S88 Batch

Defining an S88 model for your equipment and processes frees the flow of data between the business requirements and discrete automation control.

Quality control, batch analysis, and logging of process execution is the first step to feedback best practices for increased production.

Integrated Historian

In biopharma, data is king. We integrate robust data collection, storage, and reporting connectivity into each equipment control design.

On the backend, data analysis and visualization tools are available to get the most productivity from your systems.

Find out how alarm reports can reduce nuisance alerts and increase operator engagement.

Technology Focused on Secure Biopharma Automation

Lucid's proprietary tools reduce the time and effort to secure and validate Biotech and Pharmaceutical processes and data integrity with our technology to reduce entire design process from User Requirements to Operational Qualification.

The guided interface allows you to enter the main design requirements and import existing project information from some automation applications. Using templates customized to your plant, we auto-generate the majority of design documents, validation forms, and trace forms.

Included is mobile validation support, automatic test execution, and audit trails for testers.

You can now maintain both design and validation documents in a single database. Changes to the design are automatically updated in the requirements specification, test forms, and audit log.

A Focus on Secure Biopharma Automation

Reduce the time and effort to secure and validate Biotech and Pharmaceutical processes and data integrity with our technology to reduce entire design process from User Requirements to Operational Qualification.

Maintain both design and validation documents in a single database. Changes to the design are automatically updated in the requirements specification, test forms, and audit log.

About Lucid

Lucid Automation and Security delivers production critical, technically-difficult industrial automation and network projects on time.

By tackling engaging projects, creating measurable value, and making our client partners look good, we are cultivating an environment in which our employees and partners are proud to associated.

An employee-owned company located in the San Francisco Bay Area, Lucid primarily services the local biotech and pharmaceutical manufacturing industry.