ISO Certification

  KOSHER Certification Argentina For more than 15 years, as part of its mission to help the food industry comply with kosher dietary laws, IAS has been certifying a wide variety of products in South America by granting kosher certification. Kosher food is produced only under strict supervision and it should be remembered that in addition to following traditional rules and laws, additional requirements must be adhered to in order to comply with the rules and laws of each specific Jewish community or sect.  However, all kosher foods are produced under the strictest environmental and quality controls. IAS's task is simply to monitor by: 1) Closely monitor the production lines, follow them from the collection of the raw material until they are packed and ready to be distributed. 2) Periodically verify that all equipment is in perfect condition and hygienic conditions are respected 3) Ensuring that the most stringent quality controls have been implemented, along with process contro...

  About ISO 13485 in Canada ISO 13485:2016 outlines the parameters for a Quality Management System that demonstrates an organization’s capacity to supply medical devices that meet the device’s regulatory requirements and, if applicable, patient safety goals. ISO 13485:2016 is applicable to all organizations involved in the design and manufacturing of medical devices, including device manufacturers and service providers.  What does it mean to be ISO 13485 Certified? The ISO 13485 standard is a stand-alone specification. It is based on the ISO 9001:2015 structure, but it contains medical device-specific standards such as risk analysis, sterile production, rework, and traceability. An organization that has established an ISO 13485 Quality Management System (QMS) and has successfully completed all applicable requirements, as assessed by the certification body, is referred to as an “ISO 13485-certified company.”  How to Prepare Your Organization for ISO 13485 Certification ISO...

  Products that Require CE Certification in Canada Customers can have trust in your products due to CE certification in Canada. Certification CE also facilitates the entry of items into the European market. The following are some of the products that require CE certification in Canada:  Electronic and electrical devices Radio and telecommunications terminals Equipment for working under pressure Medical equipment Gas appliances and machinery Toys, games, etc. How long will it take to get CE Certification in Canada? The length of time it takes to obtain certification CE is determined by the products and their nature. Each product has its own set of testing, inspection, and documentation requirements. The paperwork that the manufacturer must submit for certification CE differ depending on the product and category. Throughout the CE certification process, IAS provides comprehensive information and support. We handle all of your certification CE needs thanks to our industry knowled...

  Who can Apply for FDA Certification? FDA registration is available to food facilities, pharmaceutical companies, dietary supplement producers, and medical device manufacturers. Manufacturers who want to sell medical equipment and medications in the United States must first register with the FDA. Cosmetics firms can also register with the FDA; however, it is not compulsory. In the United States, registration is critical for selling your goods. Although FDA certification is not necessary for food items, it is required for food production businesses. In addition, new drug and nutritional supplement products require FDA approval. The Food and Drug Administration (FDA) examines the following factors in order to approve a product: Site inspections, process inspections, and implementation of the necessary processes. Clinical trials, test results, and research papers and protocols for further study. What is the Difference Between FDA Registration and FDA Certification? The FDA has differ...

  ABOUT ISO AUDITOR TRAINING COURSES ISO auditor training courses take place at several levels and phases. IAS handles all types of ISO auditor training in a comprehensive manner, including ISO Lead Auditor Training and ISO Internal Auditor Training, thanks to its extensive auditing expertise in the field of ISO. Types of ISO Auditor Training Courses Provided by IAS ISO Lead Auditor Training This ISO auditor training course is a voluntary certification course developed for professionals or individuals with sufficient expertise who wish to become Lead Auditor certified. Delegates who attend the ISO Lead Auditor Training course will gain a better understanding of the International Standards’ requirements. Participants will learn how to conduct a First Party Audit (Internal Audit), a Second Party Audit (Supplier Audit), and a Third Party Audit (External Audit). After completing this ISO auditor training course, business professionals will be able to execute external third-party audits...

About ISO 13485 certification and its importance ISO 13485 certification is a representation of the organization that has well-designed medical devices and equipment.  This Quality Management System certification ensures employee safety and improves customer satisfaction.  It promises consistency in product quality and develops organizational competencies.  In addition, ISO 13485 certification promotes business and brings global recognition to the organization. Integrated Assessment Services (IAS) is an ISO 13485 certification body accredited by UQAS.  We are a versatile platform for auditing and issuing ISO management system certifications across numerous ISO standards and product certifications. ISO 13485 in Mexico “ISO 13485 Mexico” is sought after by organizations that want to be certified in Mexico against this standard and people seeking training and certification in the field are also looking for ISO 13485 in Mexico. Training on ISO 13485 in Mexico It is essen...