ISO 9001 standards main objective is to obtain quality management systems that will be of actual advantage to your organization to assist & manage your business successfully and put in place best practice tactic. ISO 9001 certification will give your organization the quality systems that will provide the base to better customer satisfaction, staff motivation, and continual improvement. The ISO 9001 certificate is suitable for all types and sizes of organization and is well recognized around the world as a very useful quality management system. It is suitable for organizations in all business sectors and will help your organization to improve management processes to participate locally and/or globally. The process encompasses the entire organization and requires senior management buy-in; it is not just a function of the Quality Department. To attain ISO 9001 certification your business needs to display that it can meet the regulatory requirements and submit an application to the system effectively to give genuine assistance to your customers. The Results of Certification of ISO 9001: Well defined and documented procedures improve the regularity of productivity. Quality is constantly calculated. Procedures make sure corrective action is taken whenever failings arise. Deficiency rates reduce. Deficiency is trapped in advance and is corrected at a lesser cost. Defining procedures identifies current practices that are outdated or incompetent. Documented procedures are easier for new workers to follow. Organizations preserve or increase market share, increasing sales or revenues. Benefits of ISO 9001 Certification: A well designed and implemented QMS, based on ISO 9001 has been exposed to give organizations with the following benefits: You'll know more quickly if things are going wrong, and where; you stop spending money or wasting time on the same old problems. Many problems will disappear because you know how to prevent them; if they do come up, you'll know how to fix them faster. Better management control and reporting - which means that you know how your business is doing. You will have fewer problems with failures in service or product quality. You will have reliable, repeatable processes and a general system. Your people know what to perform and how you want it done. You will have more business, because you can sell to new markets or having the support will distinguish you in the market.

CE MARKING IS THE SYMBOL OF TWO LETTERS CE SHOWN IN FIGURE IN A RIGHT WAY. USING CE MARK IS INCORRECT OTHER THEN GIVEN FORMAT. THE CE IS ABBREVIATION OF FRENCH PHRASE "CONFORMITÉ EUROPÉENE" WHICH LITERALLY MEANS “EUROPEAN CONFORMITY”. THE TERM INITIALLY USED WAS "EC MARK" AND IT WAS OFFICIALLY REPLACED BY "CE MARKING" IN THE DIRECTIVE 93/68/EEC IN 1993. "CE MARKING" IS NOW USED IN ALL EU OFFICIAL DOCUMENTS. "CE MARKING" IS A PROCEDURE THAT APPLIES TO A WIDE RANGE OF PRODUCTS AND ONE WHICH MANUFACTURERS LOCATED IN THE EUROPEAN UNION OR IMPORTERS OF GOODS INTO THE EUROPEAN UNION MUST COMPLETE. THE CE MARK IS AFFIXED TO THE PRODUCT AS THE LAST PHASE OF THIS PROCESS AND IS EFFECTIVELY A STATEMENT FROM THE MANUFACTURER (OR IMPORTER) THAT THE PROCESS HAS BEEN LUCRATIVELY COMPLETED AND THAT THE MANUFACTURED GOODS MEETS THE NECESSARY REQUIREMENTS OF THE APPLICABLE CE MARKING DIRECTIVES. EUROPEAN UNION COUNCIL HAS ADOPTED FOLLOWING DIRECTIVES: ARTICLE 1 THE FOLLOWING COUNCIL DIRECTIVES ARE HERE BY AMENDED: 1. 87/404/EEC OF 25 JUNE 1987 (SIMPLE PRESSURE VESSELS) 2. 88/378/EEC OF 3 MAY 1988 (SAFETY OF TOYS) 3. 89/106/EEC OF 21 DECEMBER 1988 (CONSTRUCTION PRODUCTS) 4. 89/336/EEC OF 3 MAY 1989 (ELECTROMAGNETIC COMPATIBILITY) 5. 89/392/EEC OF 14 JUNE 1989 (MACHINERY) 6. 89/686/EEC OF 21 DECEMBER 1989 (PERSONAL PROTECTIVE EQUIPMENT) 7. 90/384/EEC OF 20 JUNE 1990 (NON-AUTOMATIC WEIGHING INSTRUMENTS) 8. 90/385/EEC OF 20 JUNE 1990 (ACTIVE IMPLANTABLE MEDICAL DEVICES) 9. 90/396/EEC OF 29 JUNE 1990 (APPLIANCES BURNING GASEOUS FUELS) 10. 91/263/EEC OF 29 APRIL 1991 (TELECOMMUNICATIONS TERMINAL EQUIPMENT, INCLUDING THE MUTUAL RECOGNITION OF THEIR CONFORMITY) 11. 92/42/EEC OF 21 MAY 1992 (EFFICIENCY REQUIREMENTS FOR NEW HOT-WATER BOILERS FIRED WITH LIQUID OR GASEOUS FUELS) 12. 73/23/EEC OF 19 FEBRUARY 1973 (ELECTRICAL EQUIPMENT DESIGNED FOR USE WITHIN CERTAIN VOLTAGE LIMITS) HOW TO ACHIEVE CE MARK AUTHORIZATION, CE TESTING AND MEET ALL CE MARK NECESSITIES, FOR MY PRODUCTS? BASED ON PRODUCT AND NATURE OF RISK THERE ARE A SERIES OF STEPS SUMMARIZED BELOW FOR CE MARK APPROVAL. 1. DETERMINE DIRECTIVE APPLIES ON YOUR PRODUCT (IF IT’S MORE THEN ONE, HAVE TO COMPLY WITH ALL OF THEM). 2. DETERMINE THE SCOPE WHICH YOUR PRODUCT COMPLIES WITH IMPORTANT REQUIREMENT S FOR DESIGN AND MANUFACTURING IN THE APPLIED DIRECTIVE/STANDARD. 3. CHOOSE THE CONFORMITY ASSESSMENT PROCEDURE FROM THE OPTIONS (STEPS) CALLS DIRECTIVE FOR YOUR PRODUCT. THERE ARE FEW STEPS FOR CONFORMITY ASSESSMENT PROCEDURE AS LISTED BELOW. STEP 1 : INTERNAL PRODUCTION CONTROL STEP 2 : INTERVENTION OF NOTIFIED BODY STEP 3 : EC TYPE EXAMINATION STEP 4 : CONFORMITY TO TYPE STEP 5 : PRODUCTION QUALITY ASSURANCE STEP 6 : PRODUCT QUALITY ASSURANCE STEP 7 : PRODUCT VERIFICATION STEP 8 : UNIT VERIFICATION STEP 9 : FULL QUALITY ASSURANCE SOME TIMES DIRECTIVES USE A SERIES OF QUESTIONS ABOUT YOUR PRODUCT TO CLASSIFY THE LAVEL OF RISK AND REFER TO A DIAGRAM CALLED “CONFORMITY ASSESSMENT PROCEDURE”. THIS DIAGRAM INCLUDES ALL OF ACCEPTABLE OPTIONS AVAILABLE TO A MANUFACTURER TO CERTIFY THEIR PRODUCT AND AFFIX THE CE MARKING. 1. MINIMAL RISK 2. GREATER RISK

ISO 14001 standards main objective is to obtain environment management systems that help organization to minimize how their processes negatively affect the organization. Compliance with applicable laws, regulations and all other environmental regulations and continually improvement in its operations and processes. ISO 14001 and 9001 are similar to each other pertaining processes of quality management system of how a product is produced, rather than to the product itself. As with ISO 9001 certification is performed by third party organizations rather than being awarded by ISO directly. ISO 14001 is known as a common management system standard, meaning that it is appropriate to any organization looking for to improve and manage assets more effectively. This includes: Single -site companies to large incorporated companies High-risk organizations to low-risk service organizations. Manufacturing, processing and the service industries, including local governments. All industry sectors including public and private sectors Original equipment manufacturers and their suppliers. BASIC PRINCIPLES AND METHODOLOGY: THESE ARE BASED ON WELL IDENTIFIED PROCESS IN THER ORGANIZATION.. PLAN ====>>DO====>>CHECK====>>ACT (PDCA CYCLE) Plan--establish objectives and processes required Do--implement the processes Check--measure and monitor the processes and report results Act--take action to improve performance of EMS based on results ISO 14000 SERIES STANDARDS: ISO 14001 (EMS)—Requirements with guidance for use. ISO 14004 (EMS)—General guidelines on principles, systems and support techniques. ISO 14006 (EMS)—Guidelines for incorporating ecodesign. ISO 14015 (EMS) --Environmental assessment of sites and organizations ISO 14020 (EMS) series (14020 to 14025) Environmental labels and declarations ISO 14030 (EMS) discusses post-production environmental assessment ISO 14031 (EMS) Environmental performance evaluation—Guidelines ISO 14040 (EMS) series (14040 to 14049), Life Cycle Assessment (LCA) discusses pre-production planning and environment goal settings. ISO 14046 (EMS) sets guidelines and requirements for water footprint assessments of products, processes, and organizations. Includes only air and soil emissions that impact water quality in the assessment. ISO 14001 (EMS) BENEFITS: Reducing environmental impacts. Improvements in performance of organizations environmental hazardous. Higher conformance with legislative and regulatory requirements by adopting the ISO certification 14001. Minimizing the risk of regulatory and environmental liability fines and improving and improving organizations efficiencies. Reductions of wastes and consumptions of resources and operating costs etc.

ISO 9001 (Quality Management System) ISO 9001 standards main objective is to obtain quality management systems that will be of actual advantage to your organization to assist & manage your business successfully and put in place best practice tactic. ISO 9001 certification will give your organization the quality systems that will provide the base to better customer satisfaction, staff motivation, and continual improvement. The ISO 9001 certificate is suitable for all types and sizes of organization and is well recognized around the world as a very useful quality management system. It is suitable for organizations in all business sectors and will help your organization to improve management processes to participate locally and/or globally. The process encompasses the entire organization and requires senior management buy-in; it is not just a function of the Quality Department. To attain ISO 9001 certification your business needs to display that it can meet the regulatory requirements and submit an application to the system effectively to give genuine assistance to your customers. The Results of Certification of ISO 9001: Well defined and documented procedures improve the regularity of productivity. Quality is constantly calculated. Procedures make sure corrective action is taken whenever failings arise. Deficiency rates reduce. Deficiency is trapped in advance and is corrected at a lesser cost. Defining procedures identifies current practices that are outdated or incompetent. Documented procedures are easier for new workers to follow. Organizations preserve or increase market share, increasing sales or revenues. Benefits of ISO 9001 Certification: A well designed and implemented QMS, based on ISO 9001 has been exposed to give organizations with the following benefits: You'll know more quickly if things are going wrong, and where; you stop spending money or wasting time on the same old problems. Many problems will disappear because you know how to prevent them; if they do come up, you'll know how to fix them faster. Better management control and reporting - which means that you know how your business is doing. You will have fewer problems with failures in service or product quality. You will have reliable, repeatable processes and a general system. Your people know what to perform and how you want it done. You will have more business, because you can sell to new markets or having the support will distinguish you in the market.

ISO 9001 standards main objective is to obtain quality management systems that will be of actual advantage to your organization to assist & manage your business successfully and put in place best practice tactic. ISO 9001 certification will give your organization the quality systems that will provide the base to better customer satisfaction, staff motivation, and continual improvement. The ISO 9001 certificate is suitable for all types and sizes of organization and is well recognized around the world as a very useful quality management system. It is suitable for organizations in all business sectors and will help your organization to improve management processes to participate locally and/or globally. The process encompasses the entire organization and requires senior management buy-in; it is not just a function of the Quality Department. To attain ISO 9001 certification your business needs to display that it can meet the regulatory requirements and submit an application to the system effectively to give genuine assistance to your customers. The Results of Certification of ISO 9001: Well defined and documented procedures improve the regularity of productivity. Quality is constantly calculated. Procedures make sure corrective action is taken whenever failings arise. Deficiency rates reduce. Deficiency is trapped in advance and is corrected at a lesser cost. Defining procedures identifies current practices that are outdated or incompetent. Documented procedures are easier for new workers to follow. Organizations preserve or increase market share, increasing sales or revenues. Benefits of ISO 9001 Certification: A well designed and implemented QMS, based on ISO 9001 has been exposed to give organizations with the following benefits: You'll know more quickly if things are going wrong, and where; you stop spending money or wasting time on the same old problems. Many problems will disappear because you know how to prevent them; if they do come up, you'll know how to fix them faster. Better management control and reporting - which means that you know how your business is doing. You will have fewer problems with failures in service or product quality. You will have reliable, repeatable processes and a general system. Your people know what to perform and how you want it done. You will have more business, because you can sell to new markets or having the support will distinguish you in the market.

CE MARKING IS THE SYMBOL OF TWO LETTERS CE SHOWN IN FIGURE IN A RIGHT WAY. USING CE MARK IS INCORRECT OTHER THEN GIVEN FORMAT. THE CE IS ABBREVIATION OF FRENCH PHRASE "CONFORMITÉ EUROPÉENE" WHICH LITERALLY MEANS “EUROPEAN CONFORMITY”. THE TERM INITIALLY USED WAS "EC MARK" AND IT WAS OFFICIALLY REPLACED BY "CE MARKING" IN THE DIRECTIVE 93/68/EEC IN 1993. "CE MARKING" IS NOW USED IN ALL EU OFFICIAL DOCUMENTS. "CE MARKING" IS A PROCEDURE THAT APPLIES TO A WIDE RANGE OF PRODUCTS AND ONE WHICH MANUFACTURERS LOCATED IN THE EUROPEAN UNION OR IMPORTERS OF GOODS INTO THE EUROPEAN UNION MUST COMPLETE. THE CE MARK IS AFFIXED TO THE PRODUCT AS THE LAST PHASE OF THIS PROCESS AND IS EFFECTIVELY A STATEMENT FROM THE MANUFACTURER (OR IMPORTER) THAT THE PROCESS HAS BEEN LUCRATIVELY COMPLETED AND THAT THE MANUFACTURED GOODS MEETS THE NECESSARY REQUIREMENTS OF THE APPLICABLE CE MARKING DIRECTIVES. EUROPEAN UNION COUNCIL HAS ADOPTED FOLLOWING DIRECTIVES: ARTICLE 1 THE FOLLOWING COUNCIL DIRECTIVES ARE HERE BY AMENDED: 1. 87/404/EEC OF 25 JUNE 1987 (SIMPLE PRESSURE VESSELS) 2. 88/378/EEC OF 3 MAY 1988 (SAFETY OF TOYS) 3. 89/106/EEC OF 21 DECEMBER 1988 (CONSTRUCTION PRODUCTS) 4. 89/336/EEC OF 3 MAY 1989 (ELECTROMAGNETIC COMPATIBILITY) 5. 89/392/EEC OF 14 JUNE 1989 (MACHINERY) 6. 89/686/EEC OF 21 DECEMBER 1989 (PERSONAL PROTECTIVE EQUIPMENT) 7. 90/384/EEC OF 20 JUNE 1990 (NON-AUTOMATIC WEIGHING INSTRUMENTS) 8. 90/385/EEC OF 20 JUNE 1990 (ACTIVE IMPLANTABLE MEDICAL DEVICES) 9. 90/396/EEC OF 29 JUNE 1990 (APPLIANCES BURNING GASEOUS FUELS) 10. 91/263/EEC OF 29 APRIL 1991 (TELECOMMUNICATIONS TERMINAL EQUIPMENT, INCLUDING THE MUTUAL RECOGNITION OF THEIR CONFORMITY) 11. 92/42/EEC OF 21 MAY 1992 (EFFICIENCY REQUIREMENTS FOR NEW HOT-WATER BOILERS FIRED WITH LIQUID OR GASEOUS FUELS) 12. 73/23/EEC OF 19 FEBRUARY 1973 (ELECTRICAL EQUIPMENT DESIGNED FOR USE WITHIN CERTAIN VOLTAGE LIMITS) HOW TO ACHIEVE CE MARK AUTHORIZATION, CE TESTING AND MEET ALL CE MARK NECESSITIES, FOR MY PRODUCTS? BASED ON PRODUCT AND NATURE OF RISK THERE ARE A SERIES OF STEPS SUMMARIZED BELOW FOR CE MARK APPROVAL. 1. DETERMINE DIRECTIVE APPLIES ON YOUR PRODUCT (IF IT’S MORE THEN ONE, HAVE TO COMPLY WITH ALL OF THEM). 2. DETERMINE THE SCOPE WHICH YOUR PRODUCT COMPLIES WITH IMPORTANT REQUIREMENT S FOR DESIGN AND MANUFACTURING IN THE APPLIED DIRECTIVE/STANDARD. 3. CHOOSE THE CONFORMITY ASSESSMENT PROCEDURE FROM THE OPTIONS (STEPS) CALLS DIRECTIVE FOR YOUR PRODUCT. THERE ARE FEW STEPS FOR CONFORMITY ASSESSMENT PROCEDURE AS LISTED BELOW. STEP 1 : INTERNAL PRODUCTION CONTROL STEP 2 : INTERVENTION OF NOTIFIED BODY STEP 3 : EC TYPE EXAMINATION STEP 4 : CONFORMITY TO TYPE STEP 5 : PRODUCTION QUALITY ASSURANCE STEP 6 : PRODUCT QUALITY ASSURANCE STEP 7 : PRODUCT VERIFICATION STEP 8 : UNIT VERIFICATION STEP 9 : FULL QUALITY ASSURANCE SOME TIMES DIRECTIVES USE A SERIES OF QUESTIONS ABOUT YOUR PRODUCT TO CLASSIFY THE LAVEL OF RISK AND REFER TO A DIAGRAM CALLED “CONFORMITY ASSESSMENT PROCEDURE”. THIS DIAGRAM INCLUDES ALL OF ACCEPTABLE OPTIONS AVAILABLE TO A MANUFACTURER TO CERTIFY THEIR PRODUCT AND AFFIX THE CE MARKING. 1. MINIMAL RISK 2. GREATER RISK

ISO 14001 standards main objective is to obtain environment management systems that help organization to minimize how their processes negatively affect the organization. Compliance with applicable laws, regulations and all other environmental regulations and continually improvement in its operations and processes. ISO 14001 and 9001 are similar to each other pertaining processes of quality management system of how a product is produced, rather than to the product itself. As with ISO 9001 certification is performed by third party organizations rather than being awarded by ISO directly. ISO 14001 is known as a common management system standard, meaning that it is appropriate to any organization looking for to improve and manage assets more effectively. This includes: Single -site companies to large incorporated companies High-risk organizations to low-risk service organizations. Manufacturing, processing and the service industries, including local governments. All industry sectors including public and private sectors Original equipment manufacturers and their suppliers. BASIC PRINCIPLES AND METHODOLOGY: THESE ARE BASED ON WELL IDENTIFIED PROCESS IN THER ORGANIZATION.. PLAN ====>>DO====>>CHECK====>>ACT (PDCA CYCLE) Plan--establish objectives and processes required Do--implement the processes Check--measure and monitor the processes and report results Act--take action to improve performance of EMS based on results ISO 14000 SERIES STANDARDS: ISO 14001 (EMS)—Requirements with guidance for use. ISO 14004 (EMS)—General guidelines on principles, systems and support techniques. ISO 14006 (EMS)—Guidelines for incorporating ecodesign. ISO 14015 (EMS) --Environmental assessment of sites and organizations ISO 14020 (EMS) series (14020 to 14025) Environmental labels and declarations ISO 14030 (EMS) discusses post-production environmental assessment ISO 14031 (EMS) Environmental performance evaluation—Guidelines ISO 14040 (EMS) series (14040 to 14049), Life Cycle Assessment (LCA) discusses pre-production planning and environment goal settings. ISO 14046 (EMS) sets guidelines and requirements for water footprint assessments of products, processes, and organizations. Includes only air and soil emissions that impact water quality in the assessment. ISO 14001 (EMS) BENEFITS: Reducing environmental impacts. Improvements in performance of organizations environmental hazardous. Higher conformance with legislative and regulatory requirements by adopting the ISO certification 14001. Minimizing the risk of regulatory and environmental liability fines and improving and improving organizations efficiencies. Reductions of wastes and consumptions of resources and operating costs etc.

ISO 9001 (Quality Management System) ISO 9001 standards main objective is to obtain quality management systems that will be of actual advantage to your organization to assist & manage your business successfully and put in place best practice tactic. ISO 9001 certification will give your organization the quality systems that will provide the base to better customer satisfaction, staff motivation, and continual improvement. The ISO 9001 certificate is suitable for all types and sizes of organization and is well recognized around the world as a very useful quality management system. It is suitable for organizations in all business sectors and will help your organization to improve management processes to participate locally and/or globally. The process encompasses the entire organization and requires senior management buy-in; it is not just a function of the Quality Department. To attain ISO 9001 certification your business needs to display that it can meet the regulatory requirements and submit an application to the system effectively to give genuine assistance to your customers. The Results of Certification of ISO 9001: Well defined and documented procedures improve the regularity of productivity. Quality is constantly calculated. Procedures make sure corrective action is taken whenever failings arise. Deficiency rates reduce. Deficiency is trapped in advance and is corrected at a lesser cost. Defining procedures identifies current practices that are outdated or incompetent. Documented procedures are easier for new workers to follow. Organizations preserve or increase market share, increasing sales or revenues. Benefits of ISO 9001 Certification: A well designed and implemented QMS, based on ISO 9001 has been exposed to give organizations with the following benefits: You'll know more quickly if things are going wrong, and where; you stop spending money or wasting time on the same old problems. Many problems will disappear because you know how to prevent them; if they do come up, you'll know how to fix them faster. Better management control and reporting - which means that you know how your business is doing. You will have fewer problems with failures in service or product quality. You will have reliable, repeatable processes and a general system. Your people know what to perform and how you want it done. You will have more business, because you can sell to new markets or having the support will distinguish you in the market.