Electrical Testing

The AQSCERT facilities are furnished with a wide variety of electrical test equipment to verify the operating conditions of electronic components, assemblies, and products under various types of environmental conditions. Offering a full turnkey solution for your electronic and electrical testing needs. We have the expertise to provide you the information you require whether it involves active monitoring as part of a larger test program or instead stand-alone analysis of a component, board or device. Material properties such as resistance, capacitance and inductance can be determined in addition to the electrical parameters of current and voltage.

• Arc Resistance – The intent of the Arc Resistance test is to make a relative distinction between solid electrical insulating materials. The ability of the test specimens to resist an arc at a high voltage but with a weak current in the vicinity of the insulating surface is investigated. The test focuses on the time until tracking paths start to form.
• Dielectric Breakthrough/Strength – Dielectric breakthrough refers to the highest intensity of an electric field that a material can withstand without losing its composition, while Dielectric Strength refers to the lowest intensity of an electric field at which a material breaks down.
• Dielectric Constant – The capacity of a substance to keep electrical energy in proportion to the permittivity of the surrounding space is the dielectric constant. When the constant intensifies but other factors stay the same, the electric force field grows in density. Under these conditions, an object of a specific weight and measurement can hold an electric charge — as well as greater amounts of charge — for lengthier time spans. Capacitates of high value are among the materials that benefit from having high dielectric constants.
• Surface Resistivity – This is the ratio of DC voltage between the length and width of an object’s surface. Surface resistivity is among the characteristics of a given material that can be studied and assessed in order to determine the overall value of the material — which can also be compared and contrasted with the resistivity of other materials. Overall, the testing process aids in the selection of materials.
• Volume Resistivity – The volume resistivity is an inherent quality that measures how intensely a certain substance contradicts the direction of electric currents. Low-level resistivity suggests that the substance will easily permit the flow of an electric charge. The unit of resistance is known as the ohm, which is symbolized by the letter “R”. If a one-ampere current goes through a part where the voltage could be at least one volt different, the resistivity of that part is one ohm.
• Conductivity – The conductivity of an item is the level at which matter carries out electricity, such as in the rate that heat manages to travel from one point on a given object to another. If a one-ampere current goes through a part in which one volt is present, that part has a conductivity of one Siemens. In most cases, when the voltage application is steadily maintained, the CD circuit will have a relative current to the conductance. If the latter is twice as much, so too will be the current. Likewise, a 1/10 conductance will correlate to a 1/10 current.
• Thermal Coefficient of Resistance – A thermal coefficient refers to the difference in physical makeup of a substance once it has undergone a shift in temperature. Coefficients are identified for numerous processes, such as reactivity and the magnetic and electric attributes of substances. If the resistance level to electrical currents in a piece of material goes up in light of heightened temperature, it’s referred to as positive temperature coefficient (PTC).

Environmental Testing

Guarantee top performance in every condition

Environmental testing

Technical products are frequently exposed to natural, induced or combined environments like climatic and/or mechanical stresses. in some cases, every day of every week. Heat, cold, damp, wind and weather, extreme environmental conditions can have an extreme effect on how everything functions.

 What is environmental testing?

Environmental testing simulates the different climatic conditions and mechanical stress that products are exposed during their lifetime. Sometimes environmental testing will expose weaknesses in a product’s design or performance that could occur in service, particularly at extreme levels. Manufacturers are constantly striving to demonstrate that their products are safe, reliable and compliant in every operational scenario.

Why is environmental testing important?

In general, environmental tests can prove the reliability of your products. You can demonstrate that your products have the build quality to work perfectly, no matter what the conditions. During testing, possible weaknesses can be identified and product improvements can be initiated at an early stage.

While ensuring that your products perform correctly in various environmental conditions you can demonstrate compliance of your products with international regulations, thereby increasing the possibility to gain global market access quicker and much easier.

How we can help you?

With us as your partner, you can be confident that your testing needs are covered, no matter how complex your product is or to which industry sector it belongs to. With globally accredited environmental testing laboratories (EN ISO/IEC 17025), we verify the fitness for use of components, technical equipment and products.

Mixed Flowing Gas (MFG) Testing

Any product or system component that’s exposed to the air has the potential to incur damage due to atmospheric conditions and contaminants. For telecommunications, aerospace, automotive and other equipment, these conditions can lead to premature wear and potential liability issues down the line. As a result, air testing equipment has become an important part of the quality-control process.

Temperature and humidity

Temperature and humidity testing determines how components, subsystems and complete systems behave in severe environments that involve elevated temperatures and high or fluctuating relative humidity. The tests can be static with constant temperature and humidity, they can involve the cycling of both, they can be temperature-humidity bias tests (where the moisture is used to induce a failure in an electrical device) or some combination of all of these.

ISO 50001 Management System Certification

Reduce energy costs and achieve a competitive advantage

Organisations the world over are facing rising energy prices. This comes at a time of increasing competitive pressure that is forcing companies to find new ways to reduce their total overheads. Additionally, the greenhouse gas emissions produced by organisations are a growing concern. In light of these developments, organisations must find ways to manage energy use while at the same time communicating energy management efforts to an increasingly environmentally conscious public

What is ISO 50001?

ISO 50001 is a voluntary international standard that gives organisations of any size a way to systematically optimise energy performance in all processes and promote more efficient energy management. The framework is compatible with the ISO 14001 environmental management standard, which means that organisations certified to ISO 14001 will find it easy to meet the requirements of ISO 50001.

Why is ISO 50001 important?

ISO 50001 is one of the few management systems that offer measurable cost benefits to organisations. It allows your business to achieve greater transparency and promotes best practises in energy management by demonstrating how energy is consumed throughout your value chain. The ISO 50001 energy management system (EnMS) framework is widely known to improve bottom lines through systematic improvements in energy efficiency and consumption while enhancing a company’s reputation and environmental performance.

ISO 50001 audit process

How can we help you?

AQSCERT is an internationally accredited Certification Body for various management systems. We have the experience and knowledge to provide solutions that reduce cost and risks. Working in partnership with your people, our experts can identify inefficiencies in your energy management strategy.
Our ISO 50001 services

• Pre-audit (optional)

A preliminary evaluation determines which requirements your company already fulfils.

• Audit level 1 and subsequent documentation review
  We collect information on the basic EnMS processes, prepare the certification audit and check for compliant documentation.
• Certification audit

We assess the practical implementation of your company’s EnMS, including interviews with different members of staff, review of facts and figures, and site inspection.

• Awarding the certificate

The certificate is awarded, confirming that your EnMS conforms to the ISO 50001 standard.

• Surveillance audits

Our annual surveillance audits provide ongoing support in the continuous optimisation of your processes.
• Re-certification

ISO 50001 certifications are valid for three years, after which your company needs to be re-certified

Your benefits at a glance.
• Save money – through improvements in energy efficiency and reduction in energy consumption.
• Achieve world-class standards – through our certification, which enables you to benchmark, measure and report energy efficiency improvements.
• Gain a competitive edge – by promoting energy management best practices and reinforcing good energy management behaviours.
• Improve transparency – with detailed energy analyses on energy flows and consumption patterns in your organisation to clearly communicate energy management effort

ISO 22000 Food safety management

ISO 22000 certifies the food safety and the ability to handle related risks for organisations of all sizes and working in the food processing industry.
The key aspects of the service are:

• defining clear and concrete objectives of the management model
• objective verification of the effectiveness of your food safety management system
• greater traceability of products throughout the supply chain
• guaranteeing the expectations of consumers and business partners in terms of quality and safety
• demonstration of compliance with legal requirements
• effective risk management
• facilitating access to financing, and successful tender bidding

Regulatory Focus

The ISO 22000 standard is based on the HACCP method and is integrated with the main system and product standards: ISO 9001 and ISO 14001, FSSC 22000, BRC and IFS, SA 8000 and BS OHSAS 18001, Codex Alimentarius.

Certification Procedure

• Compilation of the information questionnaire
• submission of the technical/economic offer which, once accepted, constitutes a service contract
• audit at the company and related reporting
• in the event of a successful outcome of the previous phases, certification is assessed by a technical committee
• in case of successful completion of the previous phases, the certificate is delivered to the company
• annual audit to maintain the certificate.

ISO 14001:2015

Manufacturers and service providers are under pressure to make supply chains more environmentally friendly due to the growing global awareness of the environmental impact of consumer lifestyles. Organisations that align their commercial objectives with global ecological concerns stand to gain a substantial competitive advantage. This also reduces the cost of energy and material consumption, recycling, air and water emissions, and legal fees incurred by non-compliance

What is ISO 14001?

ISO 14001 is recognised as an environmental management system standard suitable for large and small organisations. Based on the Plan-Do-Check- Act methodology, it provides a systematic framework for integrating environmental management practices by supporting

Why is it important?

Beyond demonstrating your organisation is a responsible corporate citizen, certification may significantly reduce the risk of regulatory and environmental liability fines. Companies that implement the system reduce costs and improve company-wide morale, while increasing the marketability of their brand.

Your benefits at a glance?
• Improve your marketability and sales – by applying the ISO 14001 certification to your corporate documents. This can also significantly improve your bargaining position when taking part in public and private green procurement tenders.
• Reduce cost – by minimising wastage throughout the supply chain, from materials to energy consumption. ISO 14001 certification can also contribute to significantly reducing your regulatory and environmental liability.
• Enhance your reputation – with an internationally recognised certificate from TÜV SÜD that promotes your brand image and company morale.

ISO 13485 Quality Management System for Medical Devices

ISO 13485 is a quality management system standard specifically for the medical devices industry, which encompasses aspects of the ISO 9001 standard, plus additional industry-specific medical device requirements.
ISO 13485: 2016 has been harmonised against the three EU Medical Devices, so certification to this standard by an accredited certification body such as AQSCERT Product Service automatically

demonstrates compliance with specific clauses in these directives

Why certy your quality management system?

The certification of a quality management system, specifically for medical devices, to ISO 13485 proves advantageous, and in many cases essential, for medical companies which export their products to the global market. In the European Union, the fulfilment of EU Directives (e.g Active implantable Medical Devices Directive, Medical Devices Directive and In Vitro Diagnostic Directive) allows the free trade of medical devices. A significant portion of demonstrating compliance with the EU directive requirements is the establishment and independent assessment of the quality system.

The current European medical device quality system standard is EN ISO 13485:2016. When manufacturers are active in the world market, the focus on global or international standards (e.g., ISO) is not only advantageous – it may be stipulated by certain countries. For example, Canada requires that medical device manufacturers marketing their products in Canada must have a quality system certified to ISO 13485:2016.
Who is the standart for?

• Companies who currently manufacture private label medical devices, but want to eventually place these devices under their name on the market in the European Union.
• Consultancies or agencies, which design, manufacture, and assemble medical and in vitro diagnostic medical devices, as well as medical component manufacturers.
• Manufacturers of in vitro diagnostic medical devices that want to distinguish themselves, and prepare for future IVD regulatory obligations to enter the EU.

Your benefits at a glance?

• Enhanced efficiency and marketability – Formal certification of your quality management system will help you to market your products and services and to improve the efficiency of your organisation.
  • Expert partnership – Our experienced audit team has the goal of adding value to your business by identifying improvement opportunities in addition to risks from any non-conforming areas.