• ISO 9001

    ISO 9001-Quality Management System

    Among all the modern Management Systems ISO 9001- Quality Management System stands foremost in the world. This system enables the companies to maintain excellent procedures in order to meet customer needs at the global level in terms of Quality and Standards.

    Customers are increasingly becoming quality-conscious shoppers. They want to know up front that your business will meet their needs. A certified Quality Management System demonstrates your commitment to quality and customer satisfaction. Implementing a Quality Management System will help you enhance customer satisfaction, achieve consistency, and improve internal processes. It can minimize the risk that customer expectations are not met.

    The main changes in ISO 9001

    The new mode ISO 9001:2015 is similar to the previous one.

    The new standard is based on Annex SL – the new high level structure (HLS) that brings a common framework to all management system standards. This helps to keep consistency, alignment different management system standards, offer matching sub-clauses against the top-level structure and apply common language across all standards.

    The key changes in the proposed standard are:

    The emphasis on leadership

    The focus on risk management

    Emphasis on objectives measurement and change

    Communication and awareness

    Fewer prescriptive requirements

    Annex SL’s high level structure contains 10 clauses. The high-level structure proposed in Annex SL for all ISO management systems includes, in addition to the usual 3 introductory clauses, 7 basic clauses common to all management system standards. They are: context of the organization, leadership, planning, support, operation, performance evaluation and improvement. For ISO 9001, they will replace current clauses 4, 5, 6, 7 and 8. It follows the well-known PDCA cycle and the process approach from section 4 to 10, in an order that is consistent with organizational planning and process management.

    What impact to expect on your management system?

    Changes are more significant than for the previous revision the impact of the changes depends on:

    Determine what to monitor and measure

    The Management System current maturity

    The organization strategic decision to integrate more the different Management Systems

    What impact to expect on your management system?

    Train your core team (Quality Managers, Internal Auditors, CEO)

    Adapt your management processes to make them compliant

    Integrate parts of other management systems & update documentation

    Monitor the new processes, produce & analyze new KPIs. Act accordingly


    The Transition Process takes 6 to 18 months Note: Starting date to prepare transition (2nd Quarter 2015) And Dead line to move to ISO 2015 Certificate (3rd Quarter 2018). During the 3-year-transition period, the organization decides when it transitions. An organization can still be recertified to the old standard during this period. Current certificates remain valid until the end of the transition period.

    What are your benefits Of the Transition?

    Quality Management is placed at the very core of business governance

    QMS will be closely tailored to each organization specification

    The QMS will be closely aligned with the Core Business Processes to facilitate an effective implementation

    It allows all types of businesses and activity sectors to better benefit from ISO 9001

    Quality Management is placed at the very core of business governance

    It will be easier for you to meet the mandatory requirements from your customers

    Continual improvement

    Less emphasis on documents and Greater motivated employees

    You will assure to deliver high quality products and services

    You will establish sustainable relationships with all relevant stakeholders

    ; You have more freedom to develop your own way to address the requirements of the standard

    You will ensure long-lasting customer satisfaction dueto improved ‘risk-management’

    Limiting the risks involved in the operation of relevant processes

    The creation of a knowledge-database will ensure the effective internal exchange of company-owned knowledge

    Better and timely decisions based on relevant and pertinent information

    Increasing ability to meet customer and other relevant interested parties requirements

    Higher efficiency of the QMS due to higher involvement of your employees and stakeholders

    Clients’ confidence in your products and services will be strengthened

    Responsibility for quality issues will be shared between several employees

    Anticipation of future and current needs from your stakeholders will lead to an early identification of business opportunities

    Eight Quality Management Principles

    Customer focus


    Involvement of people

    Process approach

    System approach

    Continual Improvement

    Fact based decision making

    Mutually beneficial supplier relationship

  • ISO 14001:2015

    With the alarm of global warming and its consequence the human society has become serious about the ecology and its preservation. ISO 14001 EMS helps to maintain the Environment around us, by following certain management standards. Companies adopting ISO 14001 EMS are well placed against their competitors and are duly recognized at the global level.

    Environmental regulations are getting stricter, and so is the law enforcement. Customers and shareholders increasingly demand that businesses diminish the environmental impact from their business, demonstrate what they do, and how they improve. An Environmental Management System helps your organization to be in control of and successfully manage the most significant environmental aspects, e.g. emissions, waste-handling, utilize natural resources, and energy-efficiency.

    An ISO 14001 implementation and certification proves that your Environmental Management System has been measured against a best practice standard and found compliant.

    ISO 14001– It's Key Benefits

    Implementing ISO 14001 really helps your company in the following way.

    Boosts your image

    Compliance to Environmental Legislations

    Improving cost control through materials and Energy

    Reducing Environmental Incidents which results in reputation, liability etc.

    Improve Image with Authorities

    Improve Employee ethics

    Improve awareness in the society

  • OHSAS 18001

    HSAS 18001 - Occupational Health and safety Assessment Series

    Most of the leading companies in the world adopt OHSAS 18001 – Occupational Health and Safety Management Systems. It is very essential to maintain their Health and Safety Management principles and also to upkeep reputation in the global scene. Companies with the above systems have the necessary marketing edge and its helps them to stay in front when it comes to Employee Protection

    Your company's firm commitment to protect the health and safety of your employees is a distinguishing factor in a competitive market. A certified Occupational Health and Safety Management System demonstrate your determination to safeguard your employees and the environment from harmful incidents.

    An OHSAS 18001 Standard Implementation proves that your management system has been measured against a best practice standard and found compliant.

    OHSAS 18001– It's Key Benefits

    Implementing OHSAS 18001 really helps your company in the following way.

    Boosts your image

    Commitment to protection of employees and safeguard property

    Compliance to Health and Safety Legislations

    Improving cost control through reduced Incidents

    Reduce Insurance premiums

    Improve Image with Authorities

    Improve Employee ethics

    Improve awareness in the society

  • ISO 29001

    ISO 29001 – Sector specific quality management systems

    ISO/TS 29001 (published in 2003) defines the quality management system requirements for the design, development, production, installation and service of products for the petroleum, petrochemical and natural gas industries.

    Developed as a direct result of a partnership between ISO and the international oil and gas industry (led by the American Petroleum Institute - API), ISO 29001 specifically focuses on the oil and gas supply chain.

    The ISO/TS 29001 standard is based on ISO 9001 and incorporates supplementary requirements emphasizing defect prevention and the reduction of variation and waste from service providers.

    These requirements have been developed separately to ensure that they are clear and auditable. They also provide global consistency and improved assurance in the supply quality of goods and services from providers. This is particularly important when the failure of goods or services have severe ramifications for the companies and industries involved. This standard is for all organizations working within the oil and gas industry supply chain. Certification to ISO/TS 29001 ensures standardization and improvement within the sector.


    Customer loyalty

    Repeat business and referral

    Operational results such as revenue and market share

    Flexible and fast responses to market opportunities

    Costs and cycle times through effective and efficient use of resources

    Alignment of processes which will best achieve desired results

    Competitive advantage through improved organizational capabilities

    Understanding and motivation of people towards the organization's goals and objectives, as well as participation in continual improvement

    Confidence of interested parties in the objectiveness and efficiency of the organization, as demonstrated by the financial and social benefits from the organization's performance, product life cycle, and reputation

    Ability to create value for both the organization and its suppliers by optimization of costs and resources as well as flexibility and speed of joint responses to changing markets.

  • ISO 15189

    ISO 15189 - Quality and Competence in Medical Laboratories

    ISO 15189 quality standards provide an effective quality management and technical competence framework that enables medical laboratories to meet international standards for patient care and laboratory responsibility. Accredited medical laboratories enhance credibility and competency of their testing services. The ISO 15189 quality standards, when carefully planned to meet laboratory requirements, can also improve laboratory services, products and business processes.

    Medical laboratories can also benefit from the automation of business processes and controls that help obtain or continually maintain ISO 15189 quality standards. Automation also helps with the College of American Pathologists (CAP) inspections. To learn more about automating compliance with ISO 15189 quality standards, please download the following white papers.

    The benefits are listed here below:

    An ISO 15189 certification promotes development of an international reputable image for your organization through Quality Assurance and Management Systems.

    Promotes a strong degree of consistency in compliance to medical laboratory laws and legislation both from an international and national perspective.

    Fundamentally critical in promoting laboratory efficiency and responsibility for better results and service delivery.

    The certification program also has been very critical in promoting modern laboratory practices that include professionalism and expertise in conduction of medical activities in the labs.

    Ultimately promoted the growth of customer satisfaction in organizations involved in medical laboratory testing

  • ISO 22301

    ISO 22301 - Business Continuity Management

    How would you Assure Business Continuity.

    ISO 22301 specifies requirements to plan, establish, implement, operate, monitor, review, maintain and continually improve a documented management system to protect against, reduce the likelihood of occurrence, prepare for, respond to, and recover from disruptive incidents when they arise. The requirements specified in ISO 22301:2012 are generic and intended to be applicable to all organizations, or parts thereof, regardless of type, size and nature of the organization. The extent of application of these requirements depends on the organization's operating environment and complexity.

    ISO 22301 identifies the fundamentals of a business continuity management system, establishing the process, principles and terminology of business continuity management. It provides a basis for understanding, developing and implementing business continuity within your organization and gives you confidence in business-to-business and business-to customer dealings. Use it to assure key stakeholders that your business is fully prepared and you can meet internal, regulatory and customer requirements.

    The standard provides organizations with a framework to ensure that they can continue operating during the most challenging and unexpected circumstances – protecting their staff, preserving their reputation and providing the ability to continue to operate and trade.

    The benefits are listed here below:

    Establish, implement, maintain and improve your BCMS

    Meet the requirements of your business continuity policy

    Give key stakeholders confidence in your conformity and commitment to internationally recognized best practice

    Achieve BAS certification/registration of your BCMS The standard

    Safeguard key assets and maintain your reputation

    Identify impacts of operational disruption and crucial improvements

    Encourage cross-team collaboration

    Reap cost benefits from reduced insurance premiums

    Demonstrate commitment to key stakeholders

    Gain a competitive advantage against competitors in case of a major industrial crisis

    Keep your promises, even when facing a crisis, and maintain delivery of products or services


    HACCP - Hazard Analysis Critical Control Points

    Hazard Analysis Critical Control Points (HACCP) is defined to be the food detrimental elements major control points by the food and drug administrative agent. HACCP is composed as hazard analysis (HA) and critical control points (CCP). HA is to search for the hazard elements and analyze the hazard structure. HACCP is to decide the sanitation control points to control the major hazard control points after identifying the hazard elements from material supply, manufacture, processing, preservation and distribution to the end user consumption.

    In other words, HACCP is a scientific food sanitation control system to secure the safety and hygiene of food product by the effective and self-motivated hygiene control system. HACCP is the management system dealing with food safety through the following methods. Analysis and control of hazard elements from biological, chemical and physical perspectives. All food product life cycle is the object of HACCP beginning from material supply and food manufacturing to distribution and consumption.

    The benefits are listed here below:

    Sanitation control

    Food production in sanitary manner

    Concentration in the sanitation effort and effective control of food

    Economic control of food products (Reduction of defective product and customer complaints)

    Reliability in the food product

    Safe and sanitary distribution of food product

    Choice of sanitary food product through public certification

    Prevention from the food hygiene problems

    Export advantage

    Effective response to RECALL and P/L

    Advantageous inspection process

    HACCP mark indication

  • ISO 22000

    ISO 22000 - Food Safety Management Systems.

    ISO 22000 is an international standard that defines the requirements of a food safety management system covering all organizations in the food chain from "farm to fork". The standard combines generally recognized key elements to ensure food safety along the food chain, including:

    Interactive communication

    System management

    Control of food safety hazards through pre-requisite programmes and HACCP plans

    Continual improvement and updating of the food safety management system.

    ISO 22000 is a truly international standard suitable for any business in the entire food chain, including inter-related organizations such as producers of equipment, packaging material, cleaning agents, additives and ingredients.

    ISO 22000:2005 is also for companies seeking to integrate their quality management system, for example ISO 9001:2000, and their food safety management system.

    The benefits are listed here below:

    Certifying your food management system against the requirements of ISO 22000:2005 will bring the following benefits to your organization:

    Applicable to all organizations in the global food supply chain

    A truly global international standard

    Provides potential for harmonization of national standards

    Covers the majority of the requirements of the current retailer food safety standards

    Complies with the Codex HACCP principles

    Provides communication of HACCP concepts internationally

    An auditable standard with clear requirements which provides a framework for third-party certification

    Suitable for regulators

    The structure aligns with the management system clauses of ISO 9001 and ISO 14001

    Enables communication about hazards with partners in the supply chain

  • ISO 10002

    ISO 10002 - Guidelines for complaints handling in organizations

    Customer dissatisfaction can damage your business. According to recent research, an average of 25 out of 26 unhappy anonymous customers will subsequently drive away 1,560 of their friends from your business. Smart management will find ways to differentiate themselves from competitors, define customer service standards, and deliver an effective complaint handing system for their customers.

    Complaint management is challenging as there is not always a concrete solution to the problem. Success depends on how well you understand the complaint, how it is handled and if the customer is happy with the solution offered. A new release of ISO 10002 for Quality Management: Customer Satisfaction - Guideline for Complaint Handling in Organizations is an excellent customer service certificate and acts as a 'true-to-life' manual designed expressly for this purpose.

    "A complaint is an expression of dissatisfaction made to an organization, related to its products, or the complaints handling process itself, where a response or resolution is explicitly or implicitly expected." Definition from ISO 10002. ISO 10002 is relevant to any organization that wishes to exceed customer expectations, a basic requirement for businesses of all types and sizes, whether they're in the private, public or voluntary sectors.

    The benefits are listed here below:

    There are a number of benefits to implementing and certifying your customer complaints management system:

    Customer retention: By adopting the management system, your ability to retain the loyalty of your customers will be enhanced.

    Brand reputation: Implementing and certifying your complaints management system demonstrates to stakeholders that you have a real commitment to managing customer care issues and you have processes in place to handle, analysis and review complaints.

    Operational efficiency: Implementation and certification ensures a consistent approach to handling customer queries, enabling you to identify trends and eliminate the causes of complaints, as well as improve your organization's operations.

    Improved internal communications and relations: It helps you to adopt a customer-focused approach to resolving complaints and encourage personnel to improve their skills in working with customers.

    Flexibility: The standard is compatible with ISO 9001 Quality allowing you to add value and efficiency to your organization. ISO 10002 - annex A also provides guidance specifically for small businesses.

    Continual improvement: It provides a basis for continual review and analysis of your complaints-handling process, the resolution of complaints and where improvements can be made.

  • ISO 28001

    This standard provide security system that will protect people, goods, infrastructure, equipment and transportation against security incidents and other potentially devastating situations.

    It enables your organization to execute a risk assessment with supporting management tools (I.e., document controls, key performance indicators, internal audits and training) and implements the controls in accordance with the risk involved.

    The benefits are listed here below:

    Allows security to be maintained as a process so that the effectiveness of security management can be measured and improved;

    Allows management to focus resources and efforts on areas with high-risk concerns (via a security risk assessment);

    Allows management to benchmark its security management efforts with international standards and

    Demonstrates to stakeholders the commitment to implement a systematic security management.

  • BRC

    The BRC Standard provide the standardization of quality, safety and operational criteria and ensure that manufacturers fulfil their legal obligations and provide safe end product to the consumer. BRC Global Standards are now often a fundamental requirement of leading retailers.

  • ISO 27001

    ISO 27001 - Information Security Management System

    ISO 27001 Information security systems really helps all enterprises and manufactures to manage their information security management and later to the customer needs in the most apt and efficient manner. It gives the business edge orders others in the competitive business world.

    It is based on ISO 9001. In particular, the requirements for customer satisfaction and continual improvement have been modified to make them more appropriate for regulatory purposes.

    The selection of fool proof security controls to protect Information Assets and to instill confidence among customers is the need of the hour for many commercial establishments, government agencies, nonprofit organizations etc.

    The benefits are listed here below:

    Boosts your image

    Improve organizations efficiency and effectiveness

    Reducing the likelihood of information misuse.

    Compliance with legal, statutory, regulatory and contractual requirements

    Improved corporate governance and assurance to stake holders

    Risk Assessment performed

    Threats, vulnerability and likelihood of occurrence are evaluated and Impact reduced

  • ISO 13485

    ISO 13485 - Medical Devices - Quality Management System

    ISO 13485 is an international standard that defines quality management system requirements for manufacturers of medical devices. ISO 13485 contains requirements essential for organizations operating at any tier in the medical devices and pharmaceutical supply chain. The primary objective of the standard is to facilitate harmonized medical device regulatory requirements and as a result, it includes some particular requirements for manufacture, installation and servicing such as added requirements on record-control, sterilization and risk management.

    It is based on ISO 9001. In particular, the requirements for customer satisfaction and continual improvement have been modified to make them more appropriate for regulatory purposes.

    Organizations can register to ISO 13485 as a standalone or in conjunction with an ISO 9001 or other registration. An ISO 13485 certification from us demonstrates your organization's commitment to provide products and related services that consistently meet customer and regulatory requirements applicable to the medical industry.

    The benefits are listed here below:

    ISO 13485 promotes harmonization of regulatory requirements for manufacturers of medical devices on an international scale.

    A number of countries have incorporated ISO 13485 into their regulatory systems. Compliance with ISO 13485 can be used in support of regulatory compliance.

    It incorporates many of the quality management principles and delivers the benefits of an ISO 9001 based quality management system.

    Creates a competitive advantage

    Ensures a consistent and effective approach to business management

    Reduces risk factors via the use of risk management techniques

    Engages top management involvement

    Provides a robust framework for assuring product consistency

  • ISO 17020

    ISO 17020, entitled "General Criteria for the Operation of Various Types of Bodies Performing Inspection", is an internationally recognized standard for the competence of inspection bodies. ISO 17020 should not be confused with ISO 9001, which is specific to quality management systems. ISO 9001 does not require evaluation of the technical competence of an inspection body and it should not be regarded as an ‘acceptable’ alternative to ISO 17020.

    This International Standard specifies general criteria for the competence of impartial bodies performing inspection irrespective of the sector involved. It also specifies independence criteria. This standard is intended for the use of inspection bodies and their accreditation bodies as well as other bodies concerned with recognizing the competence of inspection bodies

    The benefits are listed here below:

    Uniformity in execution and reporting method for the people carrying out the activity. Reduced penalty in case of disputes

    Meeting the accreditation requirements

    Reduced customer complaints

    Proof of conforms to specified requirements

    Improved efficiency, productivity and effectiveness in the overall Inspection bodies operation,

    Improved level of motivation, co–operation, workmanship and quality awareness including competence,

    Increase of confidence in Inspection data and of personnel performing work. Greater control of processes and activities throughout Inspection bodies. Savings in terms of time and money due to reduction or elimination of the need for re–inspection / re–work etc.,

    Provide tips on analysis of data as well as perfect record keeping.

    Provide guidelines and better control for maintenance of equipment, preservation of inspection records etc

    Establish confidence of management and customers on results as well as reports and increase customer trust as well as market share.

    Better image of Inspection bodies as a Quality inspection bodies in Global market.

    Worldwide recognition and credibility.

    An ISO 17020:2012 accredited inspection body has a definite edge over competitors.

  • ISO 17024

    ISO/IEC 17024:2012 provides a global benchmark for personnel certification programmes to ensure that they operate in a consistent, comparable and reliable manner worldwide, thereby allowing individuals to have skills that translate across national lines.

    The breadth and scope of certification programmes in existence today is tremendous: programs exist for financial planners, public accountants, safety professionals, non-destructive testing experts, supply and purchasing management professionals, the construction industry, health care professionals and hundreds more.

    The updated ISO/IEC 17024:2012 standard will help organizations that certify individuals in a variety of occupations and professions protect the integrity and ensure the validity of individual certification programmes.

    The benefits are listed here below:

    ISO 17024: 2012 covers the international requirements for bodies operating certification of persons.

    It is the most acceptable standard for personnel certification schemes the world over.

    Globally accepted benchmark for organizations operating a scheme certification of persons.

    Promote consumer and public confidence in the capabilities and competence of the people who provide specialized services or who create the products that support our daily lives and livelihoods.

  • GMP

    Good Manufacturing Practice (GMP)

    A Good Manufacturing Practices (GMP) certification scheme offers independent verification and certification that the basic manufacturing practices and prerequisites necessary for the implementation of an effective Hazard Analysis Critical Control Point (HACCP) food safety program are being followed.

    GMP compliance requires minimum practical sense hygienic and processing requirements suitable to all food processing establishments. Many food industry companies have implemented the GMP certification scheme for food processing as the foundation upon which they have developed and implemented other quality and food safety management systems, such as HACCP, ISO 22000, SQF and ISO 9001.

    GMP – It's Key Benefits

    Enhancement of your food safety management system;

    Demonstration of your commitment to producing and trading safe and quality food;

    Prepare you for HACCP certification or other food safety and quality management system;

    Increase consumer confidence in your products; and

    Prepare you for assessment by regulatory authorities and other stakeholders.

  • ISO 17025

    Calibration laboratories are used to ensure that the measurements made by the manufacturer are valid and traceable to national or international standards.

    ISO/IEC 17025:2005 is the international standard used by testing & calibration laboratories, initially issued by the International Organization for Standardization in 1999 and subsequently published in 2001 & later on revised in the year 2005.

    SO 17025 incorporates all the ISO 9001 requirements that are relevant to the scope of testing and calibration services as well as specifying the technical requirements for technical competence. ISO/IEC 17025 focuses on the laboratory competence to carry out tests and/or calibrations. ISO/IEC 17025 provides guidance to owners and operators of laboratories on both quality management in a laboratory environment and technical requirements for the proper operation of a testing laboratory.

    The standard is widely used as a quality system in environmental, food, chemical and clinical testing laboratories.


    National & International recognition, Recognizes the technical competence of laboratory staff,

    Assures the client that results are technically valid,

    Provides comparability in measurements, Decision makers can rely on test result Improves staff motivation,

    Ensures better support in the event of legal challenge,

    To assist in the development of the new programmes,

    To reduce technical barriers in trade,

    Saves money by getting it right time

  • ISO 50001

    ISO 50001 - Energy Management System

    ISO 50001:2011, Energy management systems – Requirements with guidance for use, is a voluntary International Standard developed by ISO (International Organization for Standardization). ISO 50001 gives organizations the requirements for energy management systems (EnMS). ISO 50001 provides benefits for organizations large and small, in both public and private sectors, in manufacturing and services, in all regions of the world. ISO 50001 will establish a framework for industrial plants, commercial, institutional, and governmental facilities and entire organizations to manage energy. Targeting broad applicability across national economic sectors, it is estimated that the standard could influence up to 60 % of the world's energy use.

    How would you continuously improve energy efficiency?

    ISO 50001 energy management standard identifies requirements for an organization to establish, implement, sustain and improve an Energy Management System (EnMS), this enables the organization to take a deliberate approach to attaining continual improvement of energy performance.

    This new standard will establish an international structure to help manage the energy supply, uses and intake of industrial, commercial, or institutional organizations, which includes measurement, documentation and reporting, design and procurement practices for energy using equipment, systems and processes. ISO 50001 energy management standard is applicable to all aspects impacting energy use, and this can be monitored and influenced by an organization.

    Having a certification against BS EN 16001 will assist to adopt ISO 50001 faster

    ISO 50001 – It's Key Benefits

    Enables organizations to establish the systems and processes required to improve energy commandment, which includes energy efficiency, use, consumption and intensity;

    Reductions in energy cost, GHG emissions and other environmental impacts, through the systematic management of energy; and

    Demonstrate that the organization implemented sustainable energy management systems, completed a baseline of energy use, and focused on continuously improve their energy vividness.

  • SA 8000

    SA8000 is an auditable certification standard that encourages organizations to develop, maintain, and apply socially acceptable practices in the workplace.

    The most widely recognized global standard for managing human rights in the workplace is Social Accountability International’s SA8000. It is the first auditable standard, suitable for organizations of all sizes anywhere in the world, and provides a framework for assuring all of your stakeholders that social accountability is being stewarded by your management.

    The benefits

    Achieve best practice in ethical employment, trading and operations

    Engage and motivate your employees with improved morale

    Introduce greater transparency to the way you run your business

    Maintain existing business and attract new customers and investors

    Gain recognition as an socially accountable organization

  • FSC & CE Marking

    CE - marking

    The Certificate of Conformity Europe (CE Mark) is a mark to indicate that the product to which it is affixed is in conformance with EU Product Safety Directives. These EU Directives apply to all products that are to be put into service for the first time inside the European Economic Area. The CE consultants at BAS Industrial Services know exactly what is necessary and what is not required in order to attain the Certificate of Conformity for Europe for your industrial products. Many issues arise before you can use the CE Mark, such as which EU Directives and standards are applicable, who is responsible for what, is a Notified Body required, how safe are the industrial products, what manuals are needed, how can we safeguard industrial machines, etc.

    Our Services for CE-Marking, Certificate of Conformity for Europe

    BAS can assist during the whole process of obtaining your CE Marking or just a certain part of it. We offer concrete, practical suggestions, as well as advice and guidance.

    Profit from our expertise in CE-Marking for Industrial Products as follows:

    Medical Device Directive

    In-Vitro Diagnostic Device Directive

    Active Implantable Medical Device Directive

    Machinery Directive

    Pressure Equipment Directive

    Low Voltage Directive

    EMC Directive

    Transportable Pressure Equipment Directive

    Simple Pressure Vessels Directive

    Lift Directive

    Construction Products Directive

    Toys Safety Directive

    Personal Protective Equipment Directive