The importance of doing audits!
Performing ISO audits is an important practice for organizations that seek to achieve and maintain standards of quality, efficiency and compliance with international standards established by the International Organization for Standardization (ISO). There are several reasons why ISO audits are essential: In short, ISO audits are a fundamental process to ensure that an organization is […]
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The importance of ISO certification
The ISO certification (International Organization for Standardization) is an international recognition that attests that an organization has adopted and implemented standards of quality, environmental management, occupational health and safety, information security, among others. Obtaining ISO certification is an important indicator of compliance and competence for companies and organizations across a range of industries. Here are […]
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What are the main challenges faced by companies in implementing ISO 9001 and how to overcome them effectively?
The implementation of ISO 9001 can present several challenges for companies. Some of the common challenges include: To overcome these challenges, it is essential that top management is committed, that there is a systematic approach to implementation, that adequate resources are allocated, and that communication and training are effective. It is also important to seek […]
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ISO 22716 – Good Manufacturing Practices for Cosmetics
ISO 22716:2007 is the international standard for good manufacturing practices for cosmetics. This certification aims to ensure product quality, reduce recalls and ensure consumer well-being. ISO 22716 certification ensures that you implement GMP guidelines to control hazards and risks associated with cosmetic products. This ensures continual improvement throughout the supply chain. ISO 22716 is useful […]
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RDC 44
This Resolution establishes the minimum criteria and conditions for compliance with Good Pharmaceutical Practices for the sanitary control of the functioning, dispensing and commercialization of products and the provision of pharmaceutical services in pharmacies and drugstores. For the purposes of this Resolution, Good Pharmaceutical Practices are understood to be the set of techniques and measures […]
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SASSMAQ: Ensuring safety and quality in the transport of chemical products!
Have you heard about SASSMAQ? It is an acronym that represents the Health, Safety, Environment and Quality Assessment System, an important initiative for the chemical transport sector. SASSMAQ is a program that aims to ensure safety and quality during the transport of these products. It establishes strict standards and specific requirements that companies must follow […]
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ESG
ESG stands for Environmental, Social and Governance and means using environmental, social and governance factors to evaluate companies and countries on how advanced they are in terms of sustainability.Investing in ESG is investing in companies that score high on the environmental, social and corporate governance responsibility scales as determined by third parties, independent companies and […]
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ISO 22000 implementation
The implementation of ISO 22000 is essential for companies in the food sector for several reasons. First, this standard establishes a comprehensive food safety management system, addressing all stages of the production chain, from production to consumption. This includes controlling biological, chemical and physical hazards, as well as implementing contamination prevention measures. In addition, ISO […]
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GHG inventory
The Greenhouse Gas (GHG) Emissions Inventory is a tool used to measure and report the greenhouse gas emissions of an organization, company or country. The purpose of the inventory is to help understand the amount and source of greenhouse gas emissions, allowing the organization or country to set emission reduction targets and develop strategies to […]
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RDC 654
Provides for Good Manufacturing Practices for Active Pharmaceutical Ingredients. This Resolution establishes the procedures and practices that the manufacturer must apply to ensure that the facilities, methods, processes, systems and controls used for the manufacture of active pharmaceutical ingredients are adequate, in order to guarantee quality and allow their use in the preparation of products […]
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