Hackpads are smart collaborative documents. Join Hackpad Now.

Pradeep H S

724 days ago
Unfiled. Edited by Pradeep H S 724 days ago
Pradeep S WHAT DOES THE OHSAS 18001 CERTIFICATION CONTAIN?
INTRODUCTION 
        The internationally recognized standard for OHSAS 18001 in India Occupational Health and Safety Management Systems is OHSAS 18001. By implementing best-practice standards, you can assist your company in identifying and managing its health and safety risks. By obtaining OHSAS 18001 certification, your organization may show that it is dedicated to avoiding accidents, respecting the law, and improving its overall health and safety performance. Employee, client, and stakeholder confidence in your management methods may rise as a result. Additionally, it might improve the reputation of your business and provide you with a strategic advantage. An OHSMS is defined as a network of connected components. These elements include roles, power structures, connections, responsibilities, interests, endeavors, activities, processes, practices, strategies, and resources. These components set forth the OH&S policies, plans, programs, and goals.
 
What is OHSAS 18001?
        A generally recognized occupational health and safety management system (OHSMS) series standard is OHSAS 18001. Many of the top national standard-setting organizations, certification bodies, and consulting firms from around the world worked together to create the OHSAS 18001 standard. Any firm can create and maintain an OHSMS to manage the risks to its staff and others related to its activities using OHSAS 18001. Its requirements are represented in a series of terms and conditions that discuss various OHSMS components, such as risk assessment, planning controls, training and awareness, consultation and communication, operational control, emergency management and planning, incident investigation, corrective and preventive action, control of documentation, internal audits, and management reviews.
A generally recognized occupational health and safety management system (OHSMS) series standard is OHSAS 18001. Many of the top national standard-setting organizations, certification bodies, and consulting firms from around the world worked together to create the OHSAS 18001 standard. Any firm can create and maintain an OHSMS to manage the risks to its staff and others related to its activities using OHSAS 18001. Its requirements are represented in a series of terms and conditions that discuss various OHSMS components, such as risk assessment, planning controls, training and awareness, consultation and communication, operational control, emergency management and planning, incident investigation, corrective and preventive action, control of documentation, internal audits, and management reviews.
 
What is the difference between OHSAS 18001 and ISO 45001?
There are many distinctions between OHSAS 18001 consultants in Indonesia, but the most significant one is that while OHSAS 18001 was focused on controlling OH&S dangers and other internal issues, ISO 45001 focused on the relationship between a company and its business environment.
 
Objectives of OHSAS 18001:
The following are our objectives for the "Occupational Health and Safety" management system:
To promote a cooperative management structure for occupational health and safety between management and workers.
For all services, including facilities management, cleaning, security, and technological support, it is important to create and maintain safe working practices.
It is to make sure that everyone is aware of all potential risks and hazards at work and to establish precautionary measures against them.
to make sure that all employees and contractors have the necessary training to do their jobs safely and effectively.
To maintain a regular and constant interest in developing occupational health and safety performance and provide the required resources needed for the OH&S Plan's implementation and maintenance. 
 
Benefits of OHSAS 18001 
    Increase your reputation and credibility by assuring clients that you are dedicated to the effective management of occupational health and safety. You may strengthen your reputation and brand image through enhanced community relations and maintaining a positive public image. Improve cost management: Cost reduction is one thing that all organizations want. The OH&SMS can help with this by improving ratings with insurance providers and reducing occupational health and safety accidents that could result in lawsuits and damage the company's reputation. Use evidence-based decision-making, If you are using proper data to determine what to change, you can significantly enhance the likelihood that your improvements will be successful the first time, instead of requiring several failed attempts. You may rectify these improvement projects before they "run off the tracks" by using this data to track your progress, which can help you save money and time. Establish a culture of continuous improvement—By focusing on improving procedures and systematically reducing occupational health and safety risks, you can improve your company's reputation and possibly cut expenses, as mentioned above. People are regularly exploring methods to improve their processes when an improvement culture is established, which makes sustaining the OH&SMS easier. Involve your employees. OHSAS 18001 Registration in Canada Most people would want to work for the first organization when given a choice between one that shows an interest in occupational health and safety and one that does not. You can improve employee focus and satisfaction by involving them in a team effort to reduce your workplace health and safety risks.
 
What are the Certification Steps in OHSAS 18001:2007?
    Determine the documentation that requires compliance with OHSAS 18001. Integrate with the present systems, such as ISO 14001, if required. training for OHSAS 18001 if required. Internal system audits are used to implement the 18001 standards. They must also start showing up to examine the role. Review the system using the data of an internal audit. Engage with a certification organization. Stage I and Stage II audit certifications have been completed. Also, any non-conformities must be resolved. A brief assessment of the documents is done by the Certification Process. Two stages make up the registration audit:
Stage I: Conduct an on-site document evaluation of your OHSAS and determine your organization's readiness to proceed to Stage II.
Stage II: Perform an on-site audit of your complete OHSAS, which is scheduled to take place 30 to 45 days following Stage I. Any other kinds of non-conformities must be fixed before the certificate can be issued.
 
We are one of the top solutions for offering planning, consulting, and auditing for an organization that wants to maintain quality for its customers. Bringing trustworthiness certification is one of the good assets that we are trying to make for our customers with a proper producer.
 
727 days ago
Unfiled. Edited by Pradeep H S 727 days ago
Pradeep S HOW TO IMPLEMENT ISO 17025 CERTIFICATION
Introduction
        The primary ISO standard implemented by testing and calibration laboratories is ISO 17025: General Requirements for the Competence of Testing and Calibration Laboratories. The ISO 17025 Consulting Services in Nepal is the one for which most labs must be certified in order to be recognized as technically competent in most nations. In many circumstances, test or calibration results from a lab that is not certified will not be accepted by suppliers or regulatory bodies. ISO first published ISO 17025 in 1999 under the name ISO Guide 25. The most recent version of the standard is ISO 17025:2017. The Electrotechnical Commission (IEC) and the International Organization for Standardization (ISO) collaborated to publish the standard (IEC). It is a quality management system that makes sure the laboratory's results are trustworthy and credible. It is used in testing and calibration labs. Although putting ISO 17025 into practice is difficult, it is frequently necessary to guarantee that test results are accepted by clients.
        
What is ISO 17025?
ISO 17025 is described as the requirements for the capability of laboratories that conduct tests and/or calibrations. One can now conclude that the standard was developed for contract laboratories that do independent sample testing or calibrations. The standard, however, also applies to organizations that, for instance, must carry out considerations-or quality control checks as part of a production process.
Laboratories, including those operated by science and research centers, as well as others that want to implement, have already implemented, or are in the process of implementing a management system with reference to ISO 17025:2018.
 
What conditions must a laboratory satisfy to be certified by ISO 17025?
A regular external and official audit must verify the certified laboratory in order for it to remain in compliance with accreditation. The accreditation organization evaluates each ISO 17025 requirement and certifies that the laboratory conforms to it. ISO 17025 Certification in Indonesia Various requirements must be satisfied in order to receive certification. The laboratory has needs for resources, processes, and management in addition to general and structural requirements. While ISO 9001 primarily addresses management standards, ISO 17025 focuses especially on laboratories, their test procedures, and calibrations. resource requirements that apply to laboratories as well. These specify, among other things, that the individual must satisfy the appropriate requirements and that all necessary resources, including the proper space, must be made available for laboratory activities. Another important necessity for resources is the measurement traceability of laboratory data.
 
Benefits of ISO 17025
The implementation of ISO 17025:2017 has many advantages. Although achieving certification to the standard could involve some initial expenditures, it's important to realize that having ISO 17025 in place will provide you with long-term benefits, making the work well worth it.
International Recognition will be able to establish a strong reputation and demonstrate that it has excellent standards, setting it apart from competitors. Additionally, having a good reputation has Working with auditors and government regulators will assist the lab's reputation development not only locally but also nationally and worldwide. The restrictive rules of ISO 17025:2017 demand that labs closely monitor results. Obtaining consistent and efficient results aids in reducing lab operating expenses. Saving money comes from reducing the need for retesting. Overall, the standard establishes guidelines for bringing control to lab operations, which reduces operating expenses. Labs are required by ISO 17025:2017's Systematic Approach to use a systematic approach to their operations. Therefore, this helps in maintaining research and experiments. Better Lab Testing Conditions Results are more accurate when test techniques are valid and appropriate in the specified lab environment. This ensures quality for both your lab and your clients. You'll save time and money by having fewer tests performed when lab testing is improved. ISO 17025 in Canada Additionally, the standard provides strict requirements for tools and equipment, which reduces the frequency of repairs and faults. Because the ISO is a widely known standard, improved customer satisfaction levels are useful and labs will easily gain the trust of their existing and potential clients. The ISO 17025 standards make sure that your laboratory is running smoothly, consistently, and committed to giving the best results and, as a result, client satisfaction. The documentation of ISO 17025:2017 mandates proper documentation of all procedures, modifications performed, errors, or discrepancies, and assists in problem avoidance, facilitating stability and better lab outcomes. The team becomes more responsible when the proper documents are followed.
 
The time needed to obtain ISO 17025
Certification under ISO 17025 takes time. A laboratory typically needs six months to a year to get ready for the accreditation assessment. From the day that any eligible non-conformance is closed until the certificate is issued, the evaluation itself takes about 8 weeks to complete. This covers the time needed for documentation and approval as well as the Executive Committee's review.
 
We are one of the top solutions for offering planning, consulting, and auditing for an organization that wants to maintain quality for its customers. Bringing trustworthiness certification is one of the good assets that we are trying to make for our customers with a proper producer.
 
728 days ago
Unfiled. Edited by Pradeep H S 728 days ago
Pradeep S HOW TO CHOOSE AN ISO 13485 CERTIFICATION
INTRODUCTION
The standards for a Quality Management System for Medical Device Manufacturing are defined in the International Standard ISO 13485 consultant in Egypt, which ensures that all medical devices conform to legal requirements and consumer demands. The quality management standard ISO 9001, which is available to companies in a wide range of industries, is the origin of ISO 13485. However, some of the standards in ISO 9001 were difficult to apply to the medical device and pharmaceutical industries due to their unique requirements, so ISO 13485 was created to address these requirements. 
 
What is ISO 13485 Certification?
ISO 13485's certification means An organization is considered ISO 13485 Certified if it has successfully implemented an ISO 13485 Quality Management System and fulfilled it. The ISO 13485 is measured by standardized tests for the safety and efficacy of medical devices while evaluating the effectiveness and suitability of your quality management system.
The purpose of ISO 13485 is to support medical device manufacturers in developing a quality management system that establishes and maintains the efficiency of their procedures. It makes sure that medical devices are consistently designed, developed, produced, installed, delivered, and disposed of once they have served their intended purpose safely. It ensures that medical devices are consistently designed, developed, produced, installed, and distributed before being disposed of in a safe manner for their intended usage.
 
The Importance of ISO 13485: 
Medical device manufacturers, producers, and distributors must conform to ISO 13485. Additionally, since so many manufacturers need certification in order to stay in business with a customer, suppliers and service providers can improve an organization's marketability. ISO 13485 in India The implementation, management, and maintenance of your quality system are essential for consumers, stakeholders, patients and users, and regulatory authorities when it comes to the manufacturing of medical devices because patient safety strongly depends on the quality and consistency of medical products. The importance of ISO 13485 lies not only in its implementation but also in the fact that it provides a mechanism for a detailed audit to analyze the system's efficacy. The manufacturer will have more confidence in its ability to regularly achieve and maintain regulatory compliance as a result. Additionally, it can assist in reducing unpleasant surprises and failures that might affect patient safety and destroy a manufacturer's reputation.
 
Benefits of ISO 13485 Implementation
There are several benefits to implementing a quality management system for medical device manufacturing in your organization. The framework for excellent management practice provided by ISO 13485 demonstrates the organization’s commitment to producing high-quality medical equipment. To ensure that medical equipment demonstrates the same trustworthiness and quality, ISO 13485 was developed. With the use of this standard, new markets can be extended, and benefits for regulatory approval in important markets like the European Union and Canada can be achieved. Additionally, having ISO 13485 demonstrates an organization's dedication to excellent quality. Larger manufacturers of medical devices prefer working with suppliers who have an ISO 13485-certified quality management system for medical devices in operation. Due to the change made in the 2016 update to this standard, companies are now responsible for ensuring that any subcontractors agree to ISO 13485 standards as well. Subcontractors who already have ISO 13485 certification are certainly given preference. The standards documentation is made to make it easier for employees to get the information they require when they need it. The time and cost involved in product development might be reduced with the correct information available. Creating a concentrated knowledge base through the documentation of the processes related to their medical devices could also assist organizations in identifying issues, enhancing their offerings, and simplifying their production processes.
 
How to get ISO 13485 certified?
In the documentation review process, the auditors from your preferred certification body will verify that your document conforms to ISO 13485 standards. An audit report describing your compliance status as well as any issues you may have will be given to you. You will then have the chance to put the required corrective measures into place to fix the issues. This is frequently carried out throughout the allotted time for the Quality Management System's initial implementation. In the process of the main audit, By examining paperwork, records, and business processes, the certification body auditors will verify whether your current activities are in compliance with ISO 13485 as well as your own documentation. The certification authority will send auditors to look at the records you have collected through the use of quality management system processes during this audit. ISO 13485 Consultancy in Canada Records from management reviews, internal audits, and corrective actions will be one of those in this category. The auditors will give you an audit report detailing their conclusions, including whether or not your performance management appears to be successful and if it satisfies the standards of the ISO 13485 standard, once the evaluation is finished, which almost always takes a few days. In the surveillance audits, quality management should be maintained and improved in order to comply with ISO 13485, so obtaining ISO certification is not a one-time activity. For ISO 13485, there is usually a three-year audit cycle that begins with the initial certification audit, which will examine all QMS processes. Whenever the certificate is in existence, the maintenance audits actually occur a minimum of once a year. If the business decides to keep the ISO 13485 certification and the benefits it offers, the cycle will begin after the three-year certification term is completed. The certification cycle will restart with a re-certification audit that evaluates the complete system.
Implementation generally requires 4-6 months for businesses with fewer than 50 employees. It will often take 6 to 12 months for larger businesses with more than 50 employees and/or different locations because they need more documented procedures and to include more personnel.
 
 
We are one of the top solutions for offering planning, consulting, and auditing for an organization that wants to maintain quality for its customers. Bringing trustworthiness certification is one of the good assets that we are trying to make for our customers with a proper producer.
 
 
729 days ago
Unfiled. Edited by Pradeep H S 729 days ago
Pradeep S ISO 22000 IMPLEMENTATION FOR ORGANIZATION
 
INTRODUCTION
A food safety management system must meet the requirements of ISO 22000 Consultant Services in Canada to be certified. It describes the process an organization should take to prove that it can manage risks to food safety and ensure that food is safe. 
 
Who Needs ISO Certification?
ISO 22000 certification, regardless of size, applies to all organizations involved in the food chain, including feed producers, primary producers, food manufacturers, storage and transportation operators, subcontractors, and retail and food outlets. A food safety management system is becoming a requirement for suppliers of many of these food manufacturers. It is necessary if you want to sell to big retailers, supply big food firms, or enter new markets. The safety of the final product depends on each step in the food supply chain. The ISO 22000 standard clarifies requirements and standards for food safety along the whole supply chain and beyond national boundaries. All parties involved in the food supply chain, such as businesses engaged in feed production, food manufacturing, food ingredients, food transportation, food packaging, food selling (retail or wholesale), and food preparation (restaurants, grocery stores, production of food equipment, and food additives), are covered by ISO 22000. Consumers and governments are increasingly aware of the issue of food safety and are demanding accountability and assurances of food safety. Achieving ISO 22000 certification will give your customers down the chain confidence in your product. As a result, ISO 22000 becomes both a good safety tool as well as a good marketing tool and a business improvement tool.
 
Why is food safety important? 
Food is one of the essential elements for survival, and it is necessary for all living things, especially humans. They require food, and they need it pure so they can acquire all the nutrients they need. However, the modern food sector has a propensity to disregard all rules. ISO 22000 Certification services in India As a result, malnutrition is a problem for people. The establishment of strict guidelines that organizations must follow, willingly or not, is significantly assisted by ISO 22000. The certification enables them to identify risks and implement preventive or corrective measures to make products safe for consumption.
What are the benefits for my business?
Organizations can implement a food safety management system using ISO 22000 Certification, which helps them increase their overall performance in terms of food safety. The capacity to consistently supply food-related products and services that are safe and comply with regulatory standards is one of the standard's significant potential advantages. Food standards establish food safety regulations for nations and improve risk management in food safety processes.
 
What are the key elements of ISO 22000?
Management team involvement: It's not only about how the quality department manages food safety; rather, it's a top management responsibility. This ISO 22000 focuses on the management team's involvement because they are accountable for developing the overall policy. Interpersonal communication equally upstream and downstream is essential because food safety risks can be introduced at any point in the food chain. Internal communication is also an important factor in avoiding misunderstandings and reducing hazards. Common terminology can be quite useful and important in this situation. The HACCP principles are accepted by ISO 22000 Services in Egypt including the necessary programs. A strong strategy is associated with the overall hazard analysis, and an action plan is established by the necessary programs. System management: According to ISO 22000, an organized management system created in the category of ISO 9001 is always required. Companies need only create a food safety management system to conform with ISO 22000. This leads to the conclusion that you have a system that is documented and thoroughly implemented throughout your facility. It involves important programs that are effective and efficient and make sure that the environment is clean and hygienic. To identify, simultaneously avoid, and eliminate risks to food safety, the Essential Control Measure and Hazard Assessment were developed. Establish documented food safety management system processes to manage food safety within your organization, from management and business planning components to day-to-day communication and procedures that affect food safety. 
 
The Process for ISO 22000 Certification presenting a request to an ISO certification body that is approved, defining the certification's scope, performing the first analysis to confirm that the management system's fundamental structure has been implemented, The verification of ongoing improvement, resolution of non-conformance from previous audits, conformity to the standards, etc., are all included in certification audits and surveillance audits. The process of ISO 22000 Certification, takes only 3 to 15 days to complete. The procedure for ISO 22000 Certification, Re-certification after three years.
Our ISO 22000 Certification in Indonesia has accomplished, prepared, and skilled auditors who will examine your organization in accordance with ISO 22000. You can purchase ISO 22000 for a reasonable price. finishing takes 3 to 15 days. to increase customer expectations for your company as a way of showing global recognition. Our experts are available here to guide you in the best possible way.
 
 

Contact Support



Please check out our How-to Guide and FAQ first to see if your question is already answered! :)

If you have a feature request, please add it to this pad. Thanks!


Log in / Sign up