Quality management system

Management Responsibilities

₨ 2,459.00
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Management Responsibilities

Explain Management Responsibilities for the QMS including: identifying processes to include in the QMS and monitoring and measuring of those processes, determining quality goals and objectives, establishing the quality policy, communicating the quality policy and importance of meeting customer requirements, and holding Management Review.

Includes:

  • 1.2.7.0 SOP Management Review
  • 1.2.7.1 REC Management Report
₨ 2,459.00

Translate QM

 

 

 

MAN – Quality Manual

System: [Company] Quality Management System

 

File: "1.1 MAN Quality Manual.doc"

 

 

 

 

 

Version / Revision History

 

Internal Quality Auditing ISO 9001:2008 (2 Days Course)

₨ 6,885.20

Course Objectives:

All the management system standards including ISO 9001:2008, ISO 14001, OHSAS 18001, SA 8000 and QS 9000 etc requires an organizations to conduct their own internal audits by using a team of trained internal auditors. The train internal auditor can perform effective audits and identifies the area which needs improvements. In other words they are trying to detect the problems in an early stage. This course will help the auditors to gain necessary knowledge and skills to conduct the effective audits.

Event Date: 
Fri, 20/04/2012 (All day)
₨ 6,885.20

ISO 17025

ISO 17025 for Labs, testing, Inspection & Calibration services

ISO 16949

ISO TS 16949 for Automotive Industry
ISO TS 16949 is the only quality management system standard available in the world, which has been established and controlled by International Automotive Task Force (IATF)
the members of IATF includes; ISO TS 16949 is the prerequisite to supply parts or material to most of the OEMs and TIER 1 suppliers in North America, it has also been adopted very rapidly in other parts of the world. TS 16949 was basically derived from QS 9000.

ISO 13485

Medical Device QMS

ISO 13485 is a medical device quality systems standard that supplements ISO 9001:2008. The additional requirements relate to design controls, process controls (including environmental controls), special processes, traceability, record retention, and regulatory actions, which are more critical for the medical device industry. ISO 13485 is not a product standard, but a process standard.

ISO 9001:2008

Quality System Implementation

We are assisting companies in all aspects of management, but ISO 9001:2008 quality system implementation is perhaps the hottest topic. We employ a staged approach  as shown in the Outline of Program below. Our service is very flexible and can be tailor-made to the needs of individual customers.
We understand what is required by the ISO 9000:2008 Standards because we use them since they were introduced in Pakistan.

Our consultancy staff has substantial knowledge and experience in business, industry, auditing and certification technology. We have experience in the application and use of the ISO 9000:2008 series of Standards in various kind of companies in Pakistan.

In order to ensure our service is of the highest possible quality, we aim at doing things right the first time. Clients requirements are clarified and defined before the project starts.

Outline of Program
Typically, the following shows the ISO 9000:2008 Project Program necessary for helping a Company to go for ISO 9000:2008 Certification.

  1. Initial system review
  2. Assist in the preparation of a documented quality system
  3. System implementation
  4. Internal quality audit
  5. Final assessment for readiness (I.e. Pre-audit)
  6. Assist in going through the Certification Audit by the Certification Body
  7. manufacturer or distributor

What will ISO 9001:2008 do for my organization?

  • Reduced costs are obtained through:
  • Improved product reliability.
  • Better process control and flow.
  • Better documentation of processes.
  • Reductions in product scrap, rewords and rejections.
  • Documentation of the company's quality management system.
  • Using their registration to help develop and expand business, particularly those areas where registration is a prerequisite for doing business.
  • Reduction or elimination of customer audits.
  • Increased profitability/reduced costs.
  • Improved communications, both internal and external.
  • Greater awareness of quality by employees, accompanied by enhanced pride in their jobs and contribution to the company's quality system.
  • Provision of training to all personnel. Ability to remain/become competitive in the markets.
  • Elimination of redundancy.

Our Services

How do we serve !
Multi-disciplinary Project Organization

The complex nature of today's business process and decision-making need to be supported by a multi-disciplinary professional service approach. Coupled with our qualification, knowledge and experience in a broad spectrum of business processes, we have the unique capability to bring together the various management and technology disciplines needed for the project.

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