We are available with years of expertise at your site:-

1) Use our professionally designed Quality Manual, Procedures and Forms.

• Save countless hours of your time by editing these proven procedures instead of
  starting from scratch.
• These procedures document processes to meet the requirements of the standard,
  and are ready for you to tailor for your organization.

Quality Manual, Procedures and Forms

• All documented in Microsoft Word and Excel, they are easy to edit and use.
• These documents have been used by many different types of industries for successful
  registration to newly published ISO 9001 standard.

2) Physical Requirements

• We suggests our best knowledge on the construction of the plant
• We offer the better layout of plant

3) Train your employees

• We offer the most convenient and cost effective training available.
• Computer based training provides each employee with an introduction to the standard and what it means to them

Computer Based Training

• Employees can take the training at any convenient time
• Appealing visual and audio content keep the employees attention

With vast experience in consultancy service, we have etched an enviable position in the
sphere. Our consultants are well trained in their respective domain and understand
clients requirements. Some of the reason that makes us more significant than our
competitors is as follows:

• We provide proper guidance to our clients on stringent polices of quality
  organization like ISO, TQM, OHSAS, and SA.
• We assist our clients on maintaining, improving and implementing policies
  effectively
• We provide information on policy up gradation to our clients
• We also review other companies codes and conduct to aware our clients 
  

PHASE-I [TIME SPAN - 10 DAYS]

[Brief Introduction to ISO 9000 Series and Quality Management System,
Exchange of Information On Company’s existing Quality System and
Organization Structure, Appointment of M.R.]

• Introduction to ISO 9000 Series of Standards.
• Detailed know how on different clauses of ISO 9001 and their importance in
  successfully managing an organization.
• Information on Documentation required in ISO 9001 i.e. Quality Manual,
  Procedure Manual, formats, Work Instructions, etc.
• Brief discussion on benefits of implementing and maintaining ISO 9001 QMS.
• Collection of information regarding company’s existing Quality Management
  System and Finalizing Organization Structure.
• Defining Functional Responsibilities and Authorities of various personnel.
• To appoint one employee as a Management Representative (M.R.) who will look after all the documents related to ISO Quality Management System.

PHASE-II [TIME SPAN - 15 DAYS]

[Finalization of Quality Policy and Objectives, Formats for all Departments Quality Plans, Work Instructions, etc.]

• Detailed discussion with each department managers / heads on their existing records in accordance with ISO Requirements.
• Defining Company’s Quality Policy and Objectives.
• Finalization of Quality Plans, Work Instructions, etc.
• Detailed individual explanation to each staff member contributing to company’s Quality Management System about importance of recording data and maintaining the same.

PHASE-III [TIME SPAN - 15 DAYS]

[Review and Finalization of Quality Manual, Procedure Manual, etc. and Implementation of Quality Records / Formats]

• Implementation and filling up of formats and recording data as per ISO requirements.
• Preparation of Quality Manual with MR.
• Preparation of Department wise Procedures with each department’s manager / head.
• Review and finalization of Complete Quality and Procedure Manuals and getting it approved from company’s top management.
• Detailed information on company’s total documentation staff members.
• Brief session on ISO Awareness to shop floor employees to ensure one understands the importance of adhering to company’s Quality Management   System.

PHASE-IV [TIME SPAN - 10 DAYS]

[Review of Records, Training for Internal Audit and Management Review Meetings, Measurement and Monitoring Of Processes]

• To train few employees in conducting Internal Audit of ISO Quality Management System.
• Plan for Internal Audits.
• Brief Introduction of activities related to Management review Meetings.
• To explain in detail Measurements and Monitoring of Processes.

PHASE-V [TIME SPAN - 10 DAYS]

Conducting Internal Audits, Management review Meetings, Corrective and Preventive Actions, Monitoring and Measurement of Processes

• Conduct Internal Audit by Independent and Trained Personnel in a Documented Manner.
• To record the findings of Internal Audit and bring them to the attention of respective personnel.
• Submission of various quality records in MRC Meetings.
• Desired Modifications to quality system in association with documented procedures and ISO 9000 Quality Management System.
• Determine corrective and preventive actions required to be initiated in the organization.

PHASE-VI [TIME SPAN - 10 DAYS]

Pre assessment and Final Certification

• Assisting in liaison with Certifying Bodies.
• Fine tuning of documents for Pre assessment Audit.
• Implementation based on procedure and Quality Manual.
• Certification Audit by Certifying Body.