• There are no suggestions because the search field is empty.

Automation Pyramid – FAQ

Author Avatar
QbD Group
Software Solutions & Services
Pharma & Biotech
Automation Pyramid - FAQ | QbD Group
3:12

What does an automation pyramid entail?

 

An automation pyramid visualizes the integrated layers of technology used in manufacturing or industry combined with the level of control. From the bottom, where the production runs on motors, machinery, actuators, sensors and so on, to the top where the process is managed.

QbD automation pyramid on corporate levels

 

What is an ERP?

Leading and planning on an enterprise level where the software (the enterprise resource planning, or ERP) connects and provides insight in different domains, such as finance, supply, manufacture, logistics and customers. Each business process in the enterprise has a module and is part of the ERP or provides input and or output in some way. Implementation can be expensive and must in some cases be customized to fit the processes.

What is a MES?

MES stands for manufacturing execution system and it is used to monitor the manufacturing processes based on the input delivered by for example DCS, SCADA and PLC (explained below). It provides an overview of uptime, production output, real-time and historical data, etc. MES is mainly used by management to manage the production process, and is the connecting layer between ERP and SCADA/DCS/PLC.

What is a DS?

A distributed control system (DCS) monitors, controls and steers the (manufacturing) processes, such as the pumps and valves. An HMI allows the DCS to be controlled remotely. The DCS can be on the supervision or control level, depending on the design of the process. The system provides input and reports to the MES.

What is a SCADA?

The supervisory control and data acquisition (SCADA) is a system that combines the processes of level 1 and 2 and facilitates data access and control for operators from one location. This can be used to open and close pumps or valves, for example. The system provides input and reports to the MES.

What is a PLC?

A programmable logical controller (PLC) monitors, controls and (directly) steers the devices on level 0 for example the actuators, valves, motors, etc. A PLC receives data and information from the devices from level 0 and decides (according to the programmed policy) which actions to take. Nowadays, a PLC can have an HMI that allows the PLC to be controlled remotely.

What is a HMI?

The human-machine interface (HMI) allows input and output to be exchanged between the operator (human) and machine. For example a screen, keyboard or speaker via which the operator can monitor, control or steer the machine.

 

How to validate all of these systems?

 

Risk assessment determines which effort is needed to validate a system. When validating an ERP or MES, the underlying processes will mostly be part of the validation, be it direct or indirect. The scale of the validation can also be a factor in determining whether to create one or separate protocols. It’s important to involve end users and subject matter experts for each system.

 

How can QbD Group help you?

 

QbD Group has several validation specialists in its team who can help you with the validation of your product or system. Don’t hesitate to contact us for any questions concerning your validation project.

 

Stay ahead in life sciences

Keeping up with the fast-paced life sciences industry doesn’t have to be overwhelming.

Our newsletter delivers the latest insights, industry updates, and expert content directly to your inbox, helping you stay informed and make smarter decisions.

Circles-banner-short

Discover more expert content

preview_image
Whitepaper

A Complete Guide to Computer System Validation

This guide aims to bring context and define the necessary and appropriate strategies for the validation of computerized systems. Download now.
preview_image
Whitepaper

Digital Health - Exploring the landscape and future opportunities

This whitepaper informs you about digital health, key technology pillars, and new opportunities to anticipate future trends in your healthcare sector.
preview_image
Whitepaper

How to keep computerized systems in the operational phase

Ensure compliance and efficiency with best practices for maintaining computerized systems in the operational phase. Download our expert whitepaper now!
preview_image
Webinar

From Requirements to Code: a unified MDSW development cycle that covers all requirements

Watch our webinar on demand to master medical device software development. Learn about IEC standards, cybersecurity, AI integration, and FDA expectations.
preview_image
Whitepaper

Mobile health on the rise: exploring the regulatory landscape for reimbursement

This whitepaper will help you navigate the maze of the DTx regulatory environment, highlighting several important countries and regulations.
preview_image
Whitepaper

GAMP 5 Software Validation Approach for GMP, GCP and GLP regulations

Learn how to comply with GMP, GCP, and GLP regulations using the GAMP 5 Software Validation Approach. Download the whitepaper for more insights.
preview_image
Webinar

Getting Started: Overcoming Initial Obstacles in Medical Device Software Development

Watch our webinar on demand and learn about regulatory obstacles, MDR, AI Act, and best practices for medical device software development and market entry.
preview_image
Whitepaper

Standards and regulations for software used in Medical Devices

Explore the essential standards and regulations for software used in Medical Devices, including IEC 62304 and IEC 82304. Download now.
preview_image
Whitepaper

Annual Product Quality Review in Pharma

Want to learn more about the importance, benefits, and key challenges related to the Annual Product Quality Review in Pharma? Then read on quickly!
preview_image
Whitepaper

21 CFR Part 11 compliance checklist

Want to assess whether a computer system generates electronic records and uses electronic signatures, and whether the system complies with Part 11 of 21 CFR? Download this free checklist.
preview_image
Webinar

Second edition of GAMP 5: A Risk-Based Approach to compliant GxP Computerized Systems

This webinar on demand will tell you more about the second edition of GAMP 5.
preview_image
Webinar

Verification & Validation of Artificial Intelligence/ Machine Learning Medical Devices

Explore the impact of Artificial Intelligence and Machine Learning on medical device validation and verification processes.
preview_image
Whitepaper

GAMP categories for computerized systems: what are they and what are they for?

In this whitepaper, you will learn what GAMP is, what GAMP categories are for, and where to start if you are facing computerized systems validation.
preview_image
Whitepaper

EUDRALEX Volume 4 Annex 11 Compliance Checklist

Assess your computer system's compliance with EudraLex Volume 4 Annex 11 guidelines using our checklist. Download now for GMP assurance.
preview_image
Whitepaper

From V-model to Agile: how to embrace automation as part of the computerized system validation approach

This white paper explores why IT is shifting to agile, focuses on the prevalent Scrum methodology, and concludes with guidance on adapting system validation processes.