ISO Certification

ISO 14001: 2015 specifies requirements for Environmental Management System (EMS) for any organization that seeks to demonstrate compliance with laws and regulations, and conformity to environmental policy and stated objectives, ISO 14001: 2004 supports environmental protection and the prevention of pollution in the socio-economic balance.

ISO 14001:2015 is an Environmental Management System (EMS) standard. The motivation behind this standard is to support various types of associations to successfully distinguish and deal with its natural effect, improve its operational efficiencies, easier sets back the old' finances and reduction ecological obligation dangers.

ISO 14001:2015 can be used in whole or in part to systematically progress environmental management. Claims of conformity to ISO 14001:2015, however, are not suitable unless all its requirements are incorporated into an organization's environmental management system and fulfilled without exclusion.

BENEFITS OF ISO 14001:2015 CERTIFICATION

• Improving cost control through conserving input materials and energy.
• High Level Structure (HLS) to simply integrate with more than one standard.
• Client, investor, public, community assurance by demonstrating commitment.
• Assisting the attainment of permits and authorizations for local trade.

OHSAS ISO 18001:2007 Occupational Health & Safety Assurance System (OHSAS) is a prevention based safety system designed to safe guard the safety and health of employees of the Company. OHSAS 18001 is a management system that enables an organisation to control it's OH&S risks and improve it's performance.In organizations ,one of the big problems is an unhealthy and unsafe envirament for people.

OHSAS require complete review of organization’s infrastructure, the working condition, and periodic medical checkup to assess the expected health problem employees or society will face due to working in the company.

An increasing number of organizations are completing OHSAS 18001 certification as employers are under growing burden to confirm that a rigorous health and safety policy is in place which protects employees against possible occupational risks and decreases the likelihood of accidents in the workplace. By planning ahead an organization can also recognize health and safety risks and conform to health and safety legislation.

BENEFITS OF ISO 18001:2007 CERTIFICATION

• Adoption of international best practice in relation to risk management.
• Confirms legislative awareness and compliance.
• Confirms health and well-being of employees, sub-contractors and the public.
• Increases corporate image and credibility among stakeholders, regulators, customers, prospective clients and the public.

ISO 27001:2013 is an international standard certification which is known as a best practice in Information Security Management System. The certification will aid your company to manage and protect your information assets and valuable data.

ISO/IEC 27001:2013 is the international standard that describes best practice for an ISMS (information security management system). Achieving accredited certification to ISO 27001 demonstrates that your company is following information security best practice, and make available an independent, expert verification that information security is managed in line with international best practice and business objectives. ISO 27001 is supported by its code of practice for information security management, ISO/IEC 27002:2013

This standard will support your company coordinate all your security efforts both electronically and physically, coherently, cost efficiently and with consistency and prove to potential clients that you take the security of their personal / business information seriously.

BENEFITS OF ISO 27001:2013 CERTIFICATION

• Reputation improvement among stake holders, interested party and customer.
• Progress the business potential among the competitor.
• Overall Enhancement of organization reputation in the market.
• Business opportunity enhanced.

EN ISO 13485:2012 is a certification intended for organizations that deliver medical devices. The standard puts an emphasis on regulatory needs, custom requirements, risk management and maintaining actual procedures like safe design, manufacture and distribution of medical devices.

ISO 13485: 2012 is an international standard that represents the requirements for a comprehensive quality management system for the design and manufacture of medical devices. Though it is tailored to the industry's quality system expectations and regulatory necessities, an organization does not need being actively manufacturing medical devices or their components to look for certification to this standard. ISO 13485: 2012 applies to the design, development, production, installation and servicing of medical devices. Compliance is a measure of your ability to meet client and legal needs.

ISO 13485:2012, Quality Management Standard for Medical Devices is the international standard necessities for a comprehensive quality management system for the design and manufacture of medical devices. This certificate of registration from an independent organization confirms that Portal's Quality Management System has been assessed and deemed to comply with the needs of the ISO 13485:2012 standard within the scope of the following operations - namely the design, manufacture and distribution of hand-held needle-free injection devices for drug administration. A key attribute of ISO 13485 certification is that it is a regulatory precursor for global market entry.

BENEFITS OF ISO 13485:2012 CERTIFICATION

• This standard focused to progress the performance in areas like sales, product delivery, and procedure efficiency.
• It offers a systematic framework for to define, implement, measure and analyze the procedure of business operation and client opinion.
• Overall Enhancement of organization reputation in the market.
• Business opportunity enhanced.

ISO/TS 16949:2016, in conjunction with ISO 9001:2008, defines the quality management system requirements for the design and development, production and, when relevant, installation and service of automotive-related products.

It is a certification that identifies the quality needs for the development or design, production or installation and servicing of automotive related products. Having such a system would mean that your supply chain protected from technical flaws within the system.

It’s true that TS 16949:2016 has brought some substantial changes with regard to conceptions and methods, but it’s nothing too difficult. As long as companies take the time to accurately plan for the transition, and approach the procedure systematically, there’s no reason why it can’t be completed before the deadline.

BENEFITS OF TS 16949:2016 CERTIFICATION

• Integrate with other management system standards.
• Increase involvement of your leadership team.
• Get acknowledged as a world-class automotive supplier.
• Bring quality and constant development to the heart of the organization.

ISO 22000 is developed by ISO to deal with the food safety. With the increasing demand of the processed food, and other eatable products, there was a need for an internationally recognized standard that takes care of the Food Safety. Food safety is directly linked to the food borne hazards present in the food at the point of consumption.

ISO 22000 is a systematic preventive approach to food safety and pharmaceutical safety that addresses physical, chemical, and biological hazards as a means of prevention rather than finished product inspection.

The ISO 22000:2005 standard outlines Food safety management system needs for any organization in the good chain and is one of a family of standards focused at the development, implementation and development of a food safety management system.

ISO 22000 deals with the fundamentals of food safety management systems. ISO 22000:2005 deals with the needs that organizations wishing to meet the standard have to meet. It has been designed to be compatible with other management system standards like ISO 9001 and can be implemented within an integrated management system.

ISO 22000 deals with the fundamentals of food safety management systems. ISO 22000:2005 deals with the needs that organizations wishing to meet the standard have to meet. It has been designed to be compatible with other management system standards such as ISO 9001 and can be implemented within an integrated management system.

BENEFITS OF TS 16949:2016 CERTIFICATION

• Increase the business potential among the competitor.
• Progress the confidence of customer and interested party.
• Progress the credibility of product among the customer.
• Overall Development of organization reputation in the market.

HACCP certification immediately demonstrates to clients your commitment to producing or trading in safe food. This evidence-based approach can be particularly beneficial when you are subject to inspection by regulatory authorities or stakeholders.

HACCP is applicable to all kinds of organizations irrespective of size, nature or geography of all Food Chain from farm to feed, primary producers, food manufacturers, transport & storage operators and industry like producers of equipment, packaging, cleaning agents, additives, ingredients and related to food.

BENEFITS HACCP CERTIFICATION

• Conveys a degree of confidence mandatory by consumers, retailers and buyers within the food industry.
• Implement internationally acknowledged food safety system.
• Progress the credibility of product among the customer.
• Overall Development of organization reputation in the market.

The letters ‘CE’ appear on many products that are traded on the single market in the European Economic Area (EEA), consisting of the 27 member states of the EU and European Free Trade Association countries Iceland, Liechtenstein and Norway. The CE marking is mandatory for many products and attests the verification by a manufacturer that these products meet EU safety, health or environmental needs.

Unfortunately, there is no comprehensive list of the products that need a CE marking. Therefore, it is the manufacturer's responsibility to determine if a product needs a CE marking. The "New Approach Directives" are documents that contain the legislation issued by the European Commission on the necessities that need to be met and procedures that must be followed in order for a particular product to be CE marked for sales in the EU.

CE marking is a key indicator of a product’s compliance with EU legislation and allows the free movement of products within the European market. By affixing the CE marking on a product, a manufacturer is declaring, on his sole responsibility, conformity with all of the legal necessities to achieve CE marking and therefore confirming validity for that product to be sold throughout the EEA, the 27 member states of the EU and European Free Trade Association countries - Iceland, Norway, Liechtenstein and Turkey. This also applies to products made in third countries which are sold in the EEA and Turkey. However, not all products must bear the CE marking. Only those product categories subject to exact directives that provide for the CE marking are required to be CE marked.

BENEFITS HACCP CERTIFICATION

• It is a guarantee for the manufacturer that the product is safe for consumers.
• It guarantees that the product conforms to the regulations in the specific directive
• Progress the credibility of product among the customer.
• Overall Development of organization reputation in the market.