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faina71
Apr 19, 2022
In General Discussions
It allows the manufacturer to freely sale their product throughout the European Economic Area. Promotes customers health and safety Enhances product credibility Leads to improved sales and better customer satisfaction Ensures that your product complies with the essential requirements of the relevant European health, safety and environmental protection legislation Permits the withdrawal of the non conforming products by enforcement authorities Reduce liability claims, timescale and costs. ce certification malaysia
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faina71
Apr 18, 2022
In General Discussions
ISO 13485 certification is a globally-recognized quality management system standard that provides guidance for medical device manufacturers. To achieve ISO 13485 certification, a manufacturer must demonstrate that they have implemented an effective quality management system that meets the requirements of the standard. Many medical device manufacturers choose to pursue ISO 13485 certification in order to demonstrate their commitments to high-quality medical device production, patient safety, and product reliability. iso 13485 certification
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faina71
Apr 16, 2022
In General Discussions
The HACCP certification is applicable to all organizations in the food supply chain from producers to retailers. Also, it applies to the hotels, restaurants and enterprises that provide: Fruits and vegetables Dairy products Fish and fishery products Bakery and confectionery products Meat and meat products, etc. haccp certification
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faina71
Apr 14, 2022
In General Discussions
Choose the right standard: This is the first step in getting ISO certification and it is important to choose the right standard for your business. The standard should be relevant to your business and reflect your current practices. Appoint an auditor: Once you have chosen the standard, you need to appoint an auditor who will help you to get certified. The auditor will conduct an assessment of your business to check that you meet the requirements of the standard. Implement the standard: The auditor will give you a list of recommendations on how to improve your business practices and meet the requirements of the standard. You need to implement these changes and track your progress. Get certified: Once you have met all the requirements of the standard, the auditor will certify your business. This certification is valid for a certain period of time and needs to be renewed regularly. Maintaining compliance: To maintain compliance with the standard, you need to track your progress and make sure that you are meeting the requirements. You should also carry out regular audits to make sure that your business is still compliant. Read more:iso certification malaysia
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faina71
Apr 12, 2022
In General Discussions
The following are some of the products which required CE marking, Gas appliances Toy safety Pressure Equipment, Personal protective equipment etc Electrical equipment, Radio and Telecom terminal equipment Electronic Equipment Medical devices Machinery ce certification malaysia
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faina71
Apr 11, 2022
In General Discussions
Conduct audit as per the standing requirement of the Standard ISO 14001:2015 Achieve the knowledge & skills to assess an organization’s capability to manage its EMS To plan, prepare, conduct, and follow up of ISO 14001:2015 (EMS) auditing activities Help your Organization to integrate EMS into other Management Systems such as QMS, OHSMS, etc… Helps you to write the audit reports based on factual evidence and to suggest corrective action. iso 14001 lead auditor training
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faina71
Apr 09, 2022
In General Discussions
ISO 15189 Medical laboratories – Requirements for quality and competence is an international standard that establishes specific quality management system requirements for laboratories. A revised version was published in 2012 which cancels and replaces the older version released in 2007. This standard was developed by the technical committee ISO – ISO / TC 212. They commissioned the ISO 15189 working group to prepare the standard based on the details of ISO / IEC 17025:1999 (General requirements for competence of testing and calibration laboratories). This standard establishes a stringent set of quality management requirements specific to laboratories at every level of the health care system. Some of the standard objectives for laboratory operations include ensuring the quality and traceability of patient information, maintaining the safety and integrity of laboratory materials, monitoring facility environmental conditions, and supporting public health decision making. iso 15189 adalah
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faina71
Apr 08, 2022
In General Discussions
ROHS is an acronym for Restriction of Hazardous Substances. RoHS, also known as Directive 2002/95/EC, originated in the European Union and limits the use of specific hazardous materials found in electrical and electronic products. All products applicable on the EU market after 1 July 2006 must pass RoHS compliance. Substances prohibited under ROHS are lead (Pb), mercury (Hg), cadmium (Cd), hexavalent chromium (CrVI), polybrominated biphenyl (PBB) and polybrominated diphenyl ether (PBDE). Prohibited materials are harmful to the environment and contaminate landfills, and are hazardous in terms of occupational exposure during manufacturing and recycling. rohs adalah
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faina71
Apr 07, 2022
In General Discussions
ISO training is carried out at several levels and stages. With extensive audit experience in the ISO field, IAS handles all types of ISO training comprehensively such as ISO Lead Auditor Training , ISO Internal Auditor Training , ISO Awareness, and Foundation Training. pelatihan iso
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