Digital Transformation Solutions and Services for the Pharmaceutical Industry
ATS provides Industrial Automation, Manufacturing Execution Systems (MES/MOM), Serialization and Laboratory Information Systems (LIMS) solutions suitable for Pharma 4.0. Our decades of experience and understanding of the regulated industry means we know the importance of quality assurance and compliance.
Our services and solutions enable pharmaceutical manufacturers to resolve compliance corrective actions and implement continuous improvement projects through the utilization of modern manufacturing methods.
ATS has been providing industrial automation and manufacturing IT solutions within the regulated pharmaceutical sector for over 30 years. Some of our on-going Pharma 4.0 projects include; automation upgrades and Pharma MES implementations within aseptic facilities, data collection solutions for medical device manufacturers, service level agreements and manufacturing IT Consultancy.
ATS offers the Pharmaceutical industry specific solutions for process Automation, PLC, DCS, SCADA, Quality Management and Track & Trace systems.
5,000+ projects executed taking customers towards Pharma 4.0
Ability to cross-pollinate best practices across 15+ industries
Local presence in 25+ countries
Solutions implemented in accordance to GAMP standards and FDA regulations
What do we do?
- PLC, SCADA, DCS, Batch application development
- IT application development
- Testing, installation, commissioning and 24/7 Support
- Digital transformation of existing paper-based processes and systems providing end-to-end traceable history through Electronic Batch Records (EBR)
- Pharma MES solutions supported by ATS include: Siemens Opcenter Execution Pharma (SIMATIC IT eBR) & PAS-X (Werum)
- Aggregating and presenting manufacturing data in an efficient, secure and compliant manner with off the shelf solutions.
- ATS utilises solutions such as SCADA System SIMATIC WinCC V7 (Siemens), Ignition (Inductive Automation) and PI System (OSI soft) to achieve this with its customers.
- Level-2 Integration / Data Acquisition Servers (DAS).
- Plant Information Management System.
- Real-time Operational Intelligence.
- Plant to Business Integration.
- LIMS solutions are critical to the correct formulisation and release of batches in the pharmaceutical environment. ATS have direct experience implementing and optimising LIMS solutions factoring in not just the technology challenge, but also managing the impact to people, processes and structures.
- Solutions supported include: Siemens Opcenter Laboratory (SIMATIC IT Unilab), SAP based and bespoke solutions.
- Formulated Product Development is supported with Siemens Opcenter RD&L , a formula and recipe management solution that allow you to reuse approved materials and ingredients when designing a new formulation.
- ATS is a member of OPEN-SCS Working Group and active in developing solutions in accordance to this working group’s functional requirements
- ATS manages information flow and access from shop floor equipment & IT systems to wherever it is needed in the plant. It enables data analysis and reporting through contextualisation while ensuring data traceability, security & Integrity (IIoT Solutions).
- Validation services following all complaint guidelines & rich domain experience in Integration of SCADA/ MES/ OPC/ LIMS etc.
- Knowledge of 21 CFR part 11, EU annex 11, GAMP 5, GDP and cGMP guidelines.
- For security and maintainability, manufacturers are under constant pressure to ensure their automation layer is compliant and secure. ATS has extensive knowledge and expertise in upgrading PLC’s / HMI panels and compiling the programs to a version that is compatible with the newest software version.
- We leverage our platform independent expertise on Siemens, Rockwell, Emerson, GE, Wonderware, Ignition and Honeywell to migrate automation systems from one platform to another.
- Solutions supported include: Siemens Simatic S7 hardware and TIA Portal, Emerson Delta V and DeltaV Batch, SAP MII.
How do we do it?
We leverage our global presence to provide end-to-end Automation in the pharmaceutical industry around the world.
We take ownership of Pharma 4.0 projects, from Automation consulting to post-commissioning, 24/7 Support and Training. We embed quality-by-design principles in our engineering deliverable to develop robust automation and IT systems. Our quality deliverable and process compliance is certified by the Control Systems Integrators Association (CSIA), USA.
We are a flexible and reliable partner for our customers and utilize various commercial models such as On-site Support, Fixed Price Projects, Software Maintenance Agreements, Service Level Agreements (24/7) as well as Master Service Agreements.
Your Benefits as a Customer
Rapid return on investment
Compliant upgrades and implementations
Automated quality and inspection
Paperless manufacturing
Improved Overall Equipment Effectiveness (OEE)
Improved manufacturing efficiency
