Digitalization is changing everything. This evolution is seen throughout the manufacturing industry, and nowhere is it more vital than in the Medical Device Manufacturing field. As seen in this video, Camstar Medical Device Suite is the MES of choice for Medical Device Manufacturers. By eliminating an outdated paper-based system and implementing Camstar Medical Device Suite, companies soon realize the benefits of a fully electronic, self-auditing MES that streamlines the process, reduces cost and enforces product quality and compliance.
Learn Camstar details and gain greater knowledge about paperless manufacturing solutions by attending an upcoming webinar hosted by Seabrook Technology Group on Thursday, June 20, 2019 from 11:15 a.m.-12:00 p.m. EST. Register for this FREE WEBINAR by visiting this link.
manufacturing industry is often regarded as one at the forefront of technology
adoption. There are many manufacturers,
however, who continue to rely on a paper-driven process. This is especially prevalent in the small-to-medium
medical device and biotech manufacturing industries.
by nature, is a process-centric industry, so the transformation from
paper-driven processes to paperless can seem daunting, but the
benefits of incorporating a Manufacturing Execution System (MES) are numerous,
The elimination of the need for paper, saving endless time and financial resources
Full traceability of the process in an electronic format
Inherently less review time, as the MES is self-auditing
Quick analysis and characterization of the manufacturing process
Implementation of a paperless
Manufacturing Execution System allows the operators to focus on the quality of
the product and process – not on the paperwork.
An implemented MES enforces that the product is manufactured per the
Device Master Record (DMR) and captures the actual manufacturing history
regarding material consumption and production detail records (the “who, what,
Exploring further, as MES is an end-to-end software manufacturing
solution, what additional benefits are there to implementing this system into
your shop floor? How else can
decision-makers justify MES adoption and implementation? Although the following may not be at the top
of an organization’s priority list now, these additional features/benefits of
MES implementation will pay dividends in the future, and include:
NCR Execution Management and Defect Tracking. Because MES is directly on the shop floor, there is no better system to track defects and prevent mistakes in your production process. Additionally, MES will automatically stop production if defects are discovered so that the error/defect doesn’t continue to be passed through the manufacturing process.
Enforcing Procedures and Quality Specifications in Real Time. One of the worst things a manufacturer can do is pass defects down the line. This causes major issues in production, resource management, and public (and B2B) image – especially if the defect or error is passed on to the customer.
Systematic Go/No-Go. Systematic Go/No-Go can be applied to MES, which allows for the discovery of defects, procedure enforcement and immediate staff operator notification if error occurs. Because of this systematic go/no-go, ambiguity is removed from the manufacturing process.
Close Gap Between Detection Point and Point of Failure. If there are defects in the process, MES detection minimizes the cost and resource loss of the defect.
Controlled Rework Process Flows. When defects occur, they are often salvageable – with the correct re-work. Implementation of the MES system adds structure and control when a rework is required.
Adding Statistical Processing Control. For process monitoring and/or characterization, an SPC can be added to the MES system.
Utilizing MES data for metrics and root cause analysis for failures – or to drive perfect quality.
Exploring paperless manufacturing is
an opportunity for small-to-medium manufacturers to increase their competitive
advantages. Stepping into the paperless revolution creates a more secure and more
accurate process, while leading
the way to greater revenues.
In partnership with Siemens, we at
Seabrook recommend utilization and implementation of the CamstarTM
Medical Device Suite. Camstar™ Medical
Device Suite is a leading solution in the medical device and diagnostics
industry. Known for error-proofing
processes, paperless manufacturing and the creation of eDHR (Device History
Records) and eBR (Batch Records), CamstarTM Medical Device Suite has
a proven track record of helping companies excel in achieving their goals. CamstarTM Medical Device Suite
helps companies to accelerate innovation, reduce cost, and achieve the highest
quality products – all while making compliance a by-product of the excellent
It has been our experience that
companies that utilize the CamstarTM Medical Device Suite can
quickly realize significant reduction in paper cost, cycle times,
manufacturing-related complaints, scrap, and product review and release time.
Seabrook is very much looking forward to attending our partner CAMSTAR MES’s upcoming MES workshop and plant tour at Fresenius Medical Care centre in Concord, California on April 20th. Our Global Chief Operating Officer, John Dzelme – an internationally recognised expert in MES, will chair an engaging roundtable discussion on Leveraging MES for Continuous Improvement at this exclusive event.
Seabrook has been a long term partner of CAMSTAR®, a Siemens company, and we are delighted to be taking part in an event that showcases the many and considerable benefits of MES.
There will also be a tour of the Fresenius plant, where the company will demonstrate how it uses CAMSTAR® MES in its daily operations to ensure high product quality and regulatory compliance. Other discussions, which Seabrook will contribute to, include how MES can drive business decision making, lean and continuous improvement, product traceability and FDA Case for Quality.
Partnered with Siemens, Seabrook is a valued added reseller of the Camstar Medical Device Suite and has been a Camstar partner since 2006.
10 years on Camstar Medical Device Suite is still a leading solution in the medical device and diagnostics industry for error-proofing processes, paperless manufacturing and electronic device history records (eDHR). Emerging, midsize and global medical device and diagnostics organizations are faced with the challenge of balancing cost reductions and regulatory compliance while consistently producing high-quality products. Camstar Medical Device Suite has a proven track record of helping medical device and diagnostics companies excel in the face of these challenges.
Providing a powerful and flexible tool Camstar Medical Device Suite is a unique configuration of Camstar Enterprise platform. By effectively addressing the full range of business challenges that the industry faces, Camstar Medical Device Suite helps manufacturers become better, faster and cheaper. It does this by enabling you to build quality into the manufacturing process instead of testing quality coming out of the process, a mistake that often occurs in the manufacturing sector. Camstar Medical Device Suite has been deployed with powerful results in a variety of medical device product segments, such as diagnostics, orthopedics, cardiovascular, hospital and wound care, diabetes care, renal, blood care, vision and imaging. The solution is highly functional and flexible and provides an excellent user experience.
Proactively build quality into the manufacturing process
Identify, analyze, solve and prevent problems while production continues
Provide visibility into the performance of components, tests, etc.
Enable you to understand fatigue impact, manual operation failure rates and time to ramp to quality
Close the loop on continuous improvement initiatives
Define, distribute and enforce process and engineering changes to any global factory
Replace manual paper manufacturing processes with proactive manufacturing execution that streamlines the process, delivering cost reductions and improved quality and compliance. The result is a complete electronic audit trail of all manufacturing activity and an electronic device history record. There is no paper, printing, moving or storage.
Automated enforcement and control Collect information and enforce business rules to achieve error-proof processes. Ensure the right procedures, operators, equipment and materials are used within specification and in the right sequence. Move to a review by exception product release process as a result of an automated self-auditing electronic device history record.
Lean and Six-Sigma initiatives are driven by data to establish a baseline, identify improvements, analyze results and control processes. Camstar Medical Device Suite provides the foundation by enabling you to collect integrated product, process and quality data in a structured electronic format in a matter of seconds. You can make your processes mistake proof with systemic enforcement to ensure control, closing the loop on continuous improvement initiatives.
Define, distribute and enforce process and engineering changes to any global factory. Complete audit trails make it possible to understand the impact of engineering change orders (ECOs) and the effectivity of corrective and preventive actions. Intelligent root cause analysis enables you to discover the true source of the problem by leveraging a growing knowledge base of granular product design, process design, manufacturing (as-built and inspection), field use and quality event data.
Use configurable searches such as where used analysis to identify suspect at-risk material based on unique criteria, such as a component lot, machine, operator, a specific shift, etc. Configure dynamic actions based on your business rules, then take quick action, such as hold, rework, material review board (MRB), quarantine, etc. All products, components and supplied materials are completely traceable.