International Organization for standardization (ISO) certification is the symbol of premium quality, credibility and competence. ISO standard in your business activity is the best means of retaining customer loyalty and increasing brand visibility and recognition. We provide both ISO consultation and certification services to meet the benchmarks required to achieve ISO certification. With our support in each stage of ISO certification process, achieving the highest status of globally acclaimed quality standard wouldn’t be an unattainable goal for you anymore.
PveezLegal Provides following standards
ISO 9001 Quality Management
This is thecornerstone standard that organisations should have, with the most recent version being ISO 9001:2015. While there are a few standards within the ISO 9000 family (which covers quality management), the ISO 9001 is the only standard which you can be certified in.
ISO 14001 Environmental Management
This standard is designed to help organizations fulfil their obligations under the Environmental obligations Law.
ISO 45001 Health and Safety
Released in 2018, ISO 45001 is based on OHSAS 18001. Containing the basic elements of ISO 9001. Its primary function is to:
- Reduce occupational injuries and diseases
- Promote and protect physical and mental health
ISO 27001 Information Security
In both the modern workplace and individuals’ personal lives, we place a lot of our information in paper and electronic systems. ISO 27001 is designed for information security management.
ISO 22000
ISO 22000:2018 Food Safety Management Systems – Requirements for any organization in the food chain, sets out the requirements for a food safety management system.
Good Manufacturing Practices (GMP) Certification
GMP stands for Good Manufacturing Practice. Good Manufacturing Practice is a system for ensuring that products are consistently produced and controlled according to quality standards. It is promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act.
To regulate the quality and maintain the standards, it is Compulsory to register such products by law before launching (selling) them in the U.A.E market.
Product Registration is the process of registering the products with Dubai Municipality. The government of UAE regulates the manufacture, sale and import of cosmetic, Food, Electronics & Medical products. By requiring that all the products which are being used in the domestic market to be registered prior to placing in Dubai/UAE market.
Product Registration in Dubai/UAE restricts the trading of fake and harmful products in the domestic markets, to ensure the customer safety and quality of the product.
Dubai is the one of most important and leading hub of the world for trading of Cosmetics and Perfumery product; that is import and export of the cosmetic and special care products .The UAE government follows International standard for Cosmetic product registration The main purpose of cosmetic product registration in Dubai is to make sure the end user safety. The registration of a cosmetic product is valid for 5 years
Foodstuff products which are new to the FIRS program should be registered through this program. This requires a description of the packaging type (carton containers or plastic or metal etc.) and a clear image of the label and the food item itself (the size of the image should not exceed 10 MB). The labeling information should be present on the wrapper as a minimum requirement.
Health Supplements are those products that are taken by mouth to provide additional nutrition in the body. There are high standards set by the UAE Government for registration of health as well as food supplements in Dubai. This makes it easier for registered companies to launch their products in other countries also without nuisance. This system restricts and controls the entry of any harmful health supplement.
Any organization or company that wants to import, supply or manufacture detergents and disinfectants has to go through a comprehensive registration through Dubai Municipality or ESMA.
The UAE medical device registration regulations dictate that the only entities allowed to carry out medical device registration are the manufacturer of the medical device or their local representative. The UAE medical devices Registration Guidelines require a drug warehouse to register with MOHAP and possess a valid licence before commencing the process to register their devices for import and trade in the country. As for Marketing Authorisation Holder companies, they must also have the approval of the manufacturer and with MOHAP. The local representatives may only act on the manufacturer’s behalf with prior authorisation to market the product in the Emirates.
