ISO 29990: specifies basic requirements for providers of learning services within non-formal education and training.

ISO 13485: ISO 13485 specifies requirements for a quality management system for the medical devices where an organization needs to demonstrate its ability to provide medical devices.

Such organizations can be involved in one or more stages of their Life-cycle, including design and development, manufacturing, storage and supply, installation, or servicing of a medical apparatus, and design and development or provision of associated activities. 

ISO 13485:2016 can also be used by suppliers or external parties that offer a product, including quality management system-related services to such organizations.

ISO 13485 is designed to be used by organizations included in The design, manufacturing, installation, and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes.

CE Mark The Conformitè Europëenne (CE) Mark and ISO 9001 Certification in Oman has described as the European Union’s (EU) mandatory conformity marking for controlling the goods marketed in the European Economic Area (EEA) as of 1985. 

The CE marking signifies a manufacturer’s declaration that products comply with the EU’s New Approach Directives. 

These directives not only apply to products within the EU but also to products that are manufactured in or designed to be sold at the EEA. This produces the CE marking familiar worldwide even to those unfamiliar with the EEA.

There is an EU requirement that goods not in conformity with all the terms of the directives aren’t permitted to circulate into the territories of the member countries

CE marking doesn’t provide any particular information to the consumer. It’s not a quality assurance statement, but it doesn’t reveal evidence of third-party testing, and it should not be mistaken with any certification mark of the type issued by international or European notified exam bodies.

Certain directives include a choice for the Responsible organization to present a statement of conformity saying a product fulfills the requirements of the related directives.

Halal is a word Designating any object or an action that’s permissible to use or engage in, based on Islamic law. It’s the reverse of haram. And the ISO 9001 Certification in Oman term is employed to designate food seen as permissible by Islamic law. 

Halal is the Arabic word meaning lawful or permitted. About food, it is the dietary standard, as prescribed in the Qur’an (the Muslim scripture).

These conditions are commonly used in terms of Food goods, meat products, cosmetics, healthcare products, pharmaceuticals, food ingredients, and food contact materials. 

When many things are halal or haram, some things are not apparent. Further information is needed to categorize them as halal or haram.

HACCP Hazard analysis and critical control factors, or HACCP and ISO 9001 Certification in Oman is a systematic preventive Strategy To food safety by biological, compound, bodily hazards, and more recently radiological dangers in manufacturing processes which could cause the final product to be dangerous and layouts measures to reduce these risks to a safe level. 

In this manner, HACCP tries to prevent hazards instead of trying to inspect finished products for the consequences of these hazards.

The HACCP system can be used in Any Way stages of A food series, from food production and preparation procedures including packaging, distribution, etc…

HACCP and ISO 9001 Certification in Oman was recognized internationally as a logical tool for adapting conventional review methods into a contemporary, science-based, food safety system. 

According to risk assessment, HACCP plans permit both industry and authorities to devote their funds effectively by building and auditing safe food manufacturing practices.

GMP: Good Manufacturing Practice (GMP) and ISO 9001 Certification in Oman is a system for ensuring that products are consistently produced and controlled following quality standards. 

It’s designed to minimize the risks involved in any pharmaceutical manufacturing that must not be eliminated throughout testing the final product.

GLP: The OECD Principles of Good Laboratory Practice (GLP) and ISO 9001 Certification in Oman ensure the creation of high-quality and reliable test information linked to the safety of industrial chemical compounds and preparations.

SA 8000: The SA8000 and ISO 9001 Certification in Oman Standard is the world’s foremost social certification program. The SA8000 Standard and Certification System provides a platform for organizations of all kinds, in virtually any market, and in almost any country to conduct business in a means that is reasonable and decent for employees and to show their adherence to the highest social standards. 

Made by SAI in 1997 as the first credible social certification, it has led the industry for over 20 decades.

VAPT: Vulnerability Assessment and Penetration Testing (VAPT) and ISO 9001 Certification in Oman are equally security services that focus on identifying vulnerabilities in the network server, and system infrastructure. 

The two services serve another purpose and are carried out to attain different but complementary goals.