ISO 13485 certification in Cape town
About Cape town
Cape town in South Africa, The city spans across an expanse of 116 square miles. It is home to an estimated 9,103,000 people in 2020. But Cape Town isn’t just about its past, it is a contemporary city with towering buildings and pedestrian promenades. Despite being a major seat of politics and a robust economy, its charm lies in its unique location between the mountains and the sea, its vibrant populace, and the broad-minded outlook of its local inhabitants.
Cape Town is both a bustling seaport and a governing capital. Found at the tip of the Cape Peninsula, 30 miles north of the Cape of Good Hope, it holds an important history. It is known as the “mother city” of South Africa because it’s the birthplace of European settlement.
Types Of ISO Certification In Cape town
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What is ISO 13485?
13485 as a global standard, made by the International Standards Organization. It’s like ISO 9001. But, it’s specifically for medical equipment’s quality control.
It lists everything needed by those who make, supply, distribute or are connected to the medical device business.
This assures everyone that they have strong procedures and controls for selling these devices worldwide. Many places make sure medical device creators have a quality management system running.
The FDA [Food and Drug Administration] declared recently they plan to implement ISO 13485 for medical device compliance quality standards. This is aimed at simplifying regulatory demands globally and easing manufacturers’ workload.
ISO 13485’s Quality Management System allows for adherence to varied jurisdictional necessities at once. Having an ISO 13485 Quality Management System certified by an external certification body demonstrates this compliance.
Clauses ISO 13485
Let’s break down ISO 13485. It has eight parts. The first three parts provide essential information such as references and word meanings used in the standard here.
Then, from part 4 to 8, it explains how to start and keep up an ISO 13485 quality management system. Part 4 lists out the basic and documentation needs for the quality management system, like a need for a quality manual, medical devices file, document control, and record control.
Part 5 is about what the top management of a company using ISO 13485 Quality Management System needs to do, it stresses the management’s dedication to the system and a focus on the customer. It emphasizes a quality policy and planning for a quality management system.
Also, it mentions who holds responsibility and power for the system, represents the top management, and communicates quality management system details internally.
The final segment of Part 5 is about its management review. It explains what input and output are required for the management review.
Part 6 centers around resource management. It presents the needs for resource provision, human resources, infrastructure, workspace, and contamination control.
Part 7 is all about turning the plan into a product. It involves planning, customer-based processes, design and development, purchasing, production, service provision, and finally, how to keep track of monitoring and measuring equipment.
Lastly, Part 8 is totally about measurement, analysis and enhancement. It outlines the need for feedback, managing complaints, reporting to authorities, internal audits, watching and measuring processes, overseeing and measuring product, controlling non-compliant product, data analysis and improvement from corrective and preventative action.
Why ISO 13485 is essential for medical device manufacturing project?
It plays a key role in tech and trades. Both ISO and IEC 17025 help set standard methods and smooths cooperation between labs and other groups.
It also supports results being accepted globally. Benefits span from business strategy to internal growth. A few standout points include boosting client trust.
Labs accredited to ISO or IAC 17025-2017 show they can give consistent, valid results.
This proves the team’s knowledge and all results can be linked back to the global system of units. Being certified is handy it proves lab competency and reliability it helps with promotions and staffing while improving customer satisfaction. Plus, it helps labs work more efficiently and effectively.
ISO 17025 2017 version changes Impartiality, Decision rule and Process approach
The updates of the ISO 17025 version, major shifts with the revision of the main requirements for testing and calibration labs.
Starting with Impartiality, In the ISO/IEC 17025, it’s defined as objectivity. Also, there’s a note explaining objectivity means no conflicts of interest exist or they are sorted, so they can’t affect lab activities. Lab results shouldn’t look biased because of relationships of either the lab or its employees with a client. Nor should undue pressure influence lab activities.
Therefore, labs must establish a framework to handle pressures, identify and manage ongoing risk. Potential risk can come from activities, relationships of staff. Labs also need to show minimization or eradication of risk.
Consider writing down a document outlining steps to analyze potential impartiality risks, measures to minimize risk, pertinent actions, and a signed statement of laboratory integrity from top management.
This analysis needs management review and may be revised. Labs must also manage information confidentiality during activities. Customers should be notified in writing if labs plan to make any information public. Lab staff and external personnel should sign a confidentiality agreement.
The structural requirements underwent a reorganization.
Getting ISO 13485 certified means meeting higher standards than just ISO 9001, specifically for the medical field. It comes with six notable upgrades.
Better risk management ensures all risks in the process are identified. Management roles are clearly set so all involved know their duties. Staff get regular skill upgrades and help others learn too, under the enhanced training.
Keeping the facility clean and organized is important, and so is labeling and separating products. The way designs are created is improved, with clear and efficient methods for specific product types.
Suppliers are held accountable at each step in the journey, ensuring traceability. An ISO 13485 manufacturer guarantees clear leadership, hygiene, efficient methods, and responsibility.
For instance, a CT scanner for inspecting 3D printed metal parts. You need specialized machines used only for a particular material, not for other clients. Hence, the quality system highly values the isolation of all production risks. A better explanation of management duties is necessary. This means every stakeholder has well-outlined roles and responsibilities.
There’s improved training too. It implies that all quality-related staff continuously improve their skills and guide others.
ISO 13485:2016 Certification comes with some benefits
- It promises a steady and efficient way of running a business.
- It brings down the dangers by using good old management tricks.
- You'll gain a competitive advantage and attract top executives
- Plus, you can rely on it to keep your product quality stable.
ISO 13485's Objectives
- Regulatory Compliance : It fulfills legal and rules in the medical device sector.
- Emphasizes Risk Management : It deals with risks from medical devices during product lifespan.
- Validation and Verification : Products are thoroughly tested and checked to fulfill necessary requirements.
- Traceability Focus : Keeping detailed records of product materials and methods.
- Design and Development Control : Proper plan, validation, and verification for product designs are key.
- Process Validation : Verification of manufacturing methods to maintain consistent product quality.
- Scope and Application : This is what sets ISO 9001 and ISO 13485 apart. ISO 9001 fits all organization sizes and industries, while ISO 13485 focuses on the medical device industry.
Internal Auditing in ISO 13485
Internal audits and ISO in the medical device industry, Internal audits are key for checking if a company’s processes meet ISO standards. These audits help improve and maintain rules.
How internal audits work and why they matter for medical devices under ISO. They’re more than just ticking a compliance box. They’re a strategic tool for companies to test how good their quality control system is, spotting places to get better and making sure they stick to ISO rules.
Why conducting internal audits in ISO terms is beneficial?
They’re more than just a compliance tool. It’s an opportunity to asses quality management system, find places for improvement, and make sure we’re following ISO 13485 rules. They also help improve understanding of quality processes in the company.
ISO Clause 9.2 deals with internal audits. ISO 9.2 asks companies to conduct internal audits that are systematic, independent and documented. This means gathering and assessing audit evidence objectively to check the quality management system against the plans keeping ready for your internal audits under ISO. You’ll need to work out how often to audit, the scope, and the methods, pick the right people, and set clear criteria for the audit.
When you conduct the audit, start with a meeting laying out goals and expectations, gather information and evidence during the audit, engage with staff to understand processes and gather insights, check documents, records and procedures to ensure everything is in compliance. Scrutinizing ISO-specific documentation is a crucial part of internal audits.
This includes checking the documented information against the real practices, ensuring documented procedures stick to ISO standards and making sure records are correct, complete and maintained. You might find some issues, where processes do not meet ISO standards while auditing.
When that happens, note down and document these issues, find out the root causes and develop and implement ways to correct these issues effectively. After all the activities of the audit are concluded, hold a closing meeting summarizing finding, discuss corrective actions and provide recommendations for improvement, and after the meeting, report your findings, conclusions, and recommendations in a thorough audit report.
Internal audits aren’t just about compliance. They’re also a way to continually improve. Companies should use audit outcomes to make positive changes, improve processes and increase QMS effectiveness in accordance with ISO.
Some best practices for internal audits under ISO 13485
- Make sure auditors are impartial and objective
- Train auditors to make them better at their jobs
- Customize your audit program based on risk and priorities specific to the medical device industry.
- Engage employees at all levels in the audit process to improve understanding and collaboration.
Internal auditing for ISO is over and above a requirement. It’s a strategic tool for organizational improvement. By conducting thorough and objective audits, you set the path for continued excellence in your quality management practices within the medical devices field.
Difference between ISO 9001 and ISO 13485
ISO 9001 and ISO 13485 are important quality standards. However, each is designed for a specific industry. ISO 9001 improves quality in most industries, while ISO 13485 satisfies the strict needs of the medical device industry. Knowing these differences is key for companies trying to meet these standards and create a solid quality culture.
ISO 13485 adapts to fulfil the medical device sector’s rigid requirements. Grasping these variances is key for companies for focusing on compliance and instilling quality in their industries.
The ISO 13485 certificate is vital for medical device producers. It’s usually a legal or regulatory necessity to sell medical apparatus in multiple countries.
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