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  Its first steps in your Quality Management System  transition or implementation project is to compare your current QMS to the requirements of the ISO 9001 standard.Is mentioned as Gap Analysis. The steps to be covered before conducting the Gap Analysis: Identify  peoples to conduct the Gap Analysis;they need to have some quality system experience or audit experience. You may also want to provide assistance from a us. Create or consultant with us to get a Gap Analysis Checklist.                   For more information on above content. All you need just call on  9655711335  or email us                    on  mkt.ennconsultancy@gmail.com .  We are happy to help you # chooseusaddvalue .

              The new transition includes a requirement key context in order to better                                                                            M anagement of risk on the Organisation.                                                    Special Importance  made on leaders within organizations to promote                                               environmental management.                        Shift towards improving environm...

                   As ISO Standards regularly reviewed for every 5 - 7 years approximately. This is to          help your organisation to improve in the current situations.As the transition should be implemented in              3 years with in the release date which is before 20th september 2018 to continue comply with the                  ISO 9001. Transition can be done at any time in that period but the efficient way to do is while                      recertification.                                                    For more information on above on ISO 9001: 2015 TRANSITION. All you need just call           ...

        Our Valuable customer                This what keeps us going , we will keep on improving our performance in upcoming projects,                   get more and more reviews and grow standards .                    Our Enn Consultancy team thank IMAGEICON valuable feedback . If youintersted on our service just call on  9655711335  or email us on  mkt.ennconsultancy@gmail.com .  We are happy to help you. follow us on # chooseusaddvalue .

         GMP is nothing but Good Manufacturing Practice regulations spread by the US Food and Drug Administration under the authority of  Federal Food , Pharmaceutical and Cosmetic Act. Under these regulations the force of law , require that producers, processors , and packers of  pharmaceuticals, medical devices, some food and blood which are undergone these stages in safe, pure and effective.            Good Manufacturing Practice is planned to minimize risks involved in any pharmaceutical production that cannot be detected on the final product testing. So GMP covers all guidelines address   risk including record keeping, personnel qualifications, sanitation, equipment verification, process and complaint handling.  For more information on above content. All you need just call on  9655711335  or email us on  mkt.ennconsultancy@gmail.com .  We are happy to help you # chooseusaddvalue ...

             Hazard Analysis and Critical Control Point (HACCP) is a globally recognized system for reducing the risk of safety hazard  in food industries. This certification is a proof for an organisations in the food chain continuously  controls and guarantees the surety and suitability of the food products produced in you organisation. It applies to the food product industries which  undergoes production , processing or distributing not only food and beverages, but also raw materials and auxiliary materials such as food colouring and flavouring used on the preparation of a products .            For more information on HACCP. All you need just call on  9655711335  or email us                                       on  mkt.ennconsultancy@gmail.com .  We are happy to help you # choo...

          As we have gone through Management System Certification in our past few blogs. Lets go briefly into Product Certifications. CE ( European Conformity)                   The letter “CE” it a shortened form of French phrase " C onformité   E uropéene" which means European conformity . This lettering shows the product sold in EEA (European Economic Area) been tested to meet High safety , health and environment protection requirements. Its also considered as a trade passport your products for 30 Countries of EEA.               CE- certified products can be sold and circulated throughout the entire European countries without any other national approvals. This removes significant trade difficulties. The distributors is responsible for the conformity and pattern of products manufactured outside the EU.     ...