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Shiftconnector®

Digital transformation for the pharmaceutical industry.

Shiftconnector® helps pharmaceutical manufacturers enable a 24/7 collaboration culture to drive process improvements, for better ensure quality, productivity and compliance.

  • Agile Shift Collaboration: Reduce multiple communication tools and documents to just one single source of truth – made for 24/7 manufacturing use cases.
  • Compliance: Simplify reporting and documentation with a validated solution for compliance with GxP and FDA 21 CFR Part 11 requirements.
  • Process improvement: Get real-time, actionable information for fewer lost batches, better quality control and reduced time to market.
  • Productivity: Streamline workflows and improve communication within and between teams and across shifts.
  • Compliance: Developed according to GAMP5, GxP and FDA 21 CFR Part 11 requirements.
See what Shiftconnector® can do for you.

See Shiftconnector® in action.

GxP compliance and operational excellence with Shiftconnector®

Increase batch productivity.

Shiftconnector® provides complete transparency into batch processes to drive quality and productivity improvement.

  • Plant, batch and equipment status reports
  • Infoboard for up-to-date information and change instructions
  • Overall equipment effectiveness (OEE) for batch processing units
  • Shiftconnector® GO for instant reporting during operations inspection rounds

Improve communication & documentation.

Communication is simple and efficient with one central place for all the critical information that needs to be exchanged between shifts and teams.

  • Interactive shift report with customizable templates
  • 360° overview of all events and hints
  • Binding and documented handover of responsibility for the next shift

Ensure GxP and FDA compliance.

Auditable and traceable communication, which is not part of the product documentation but relevant to be captured seriously. Where email and Office documents are not appropriate and will be replaced by an application that is designed for 24/7 shift manufacturing.

  • Supports GxP and FDA 21 CFR Part 11
  • Software application developed in accordance with GAMP5.
  • Electronic signature management (“Read and Understood”) to make communication robust. E.g., for instructions which are not part of the batch itself but must be ensured to be read by the shift operators.
  • Supports an agile world, where volatility of supply chains increases, and new medicine must be made available to the patients.

Streamline workflows.

Shiftconnector® drives efficiency and productivity by streamlining event recording, documentation and task creation standard work and records its execution.

  • Daily task lists for teams, shifts and individuals
  • Simple logging and reporting mechanism for required documentation 
  • Specific standard work checklists to ensure compliance and worker safety

Reduce operational risk.

Real-time information keeps everyone in the loop for improved accountability, responsiveness, safety and quality control.

  • Communication is an important layer of protection in an agile manufacturing environment
  • Simple recording, reporting and delegation of safety and quality information for each shift
  • Seamless communication between manufacturing, quality assurance and maintenance

Drive operational excellence.

Real-time data and reporting let you visualize key operations parameters and operational metrics for informed decision making and accountability.

  • Data analysis and visualization in shift reports
  • MES and SCADA interface to add a communication layer on top of your mission critical systems
  • Integrates with your CMMS (e.g., SAP PM or IBM Maxim o) to allow a single source of truth for the manufacturing team

Shiftconnector® io.Equipment

Digitize equipment logs and simplify documentation management with a GxP-compliant solution.

Our clients in the pharmaceutical industry.

Keep learning.

Want to learn more about Shiftconnector®? Check out the resources below or contact us for a demo.

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