QMS Implementation

 

 

A quality management system (QMS) consists of the organizational structure, procedures, processes and resources needed to implement quality management.

QMS establishes an organization's quality policy, objectives and procedures.

By implementing QMS, an organization aims to reduce and eventually eliminate nonconformance to specifications, standards, and customer expectations in the most cost- effective and efficient manner.

 

 

We will help you to generate necessary documentation, including:

  •          Quality Policy
  •          Quality Manual
  •          Standard Operating Procedures (SOPs)
  •          Material Specifications for products
  •          Material Safety Data Sheet (MSDS) for products
  •          Validation Protocols: IQ,OQ, and PQ for equipment
  •          Change Controls, Deviations, Corrective Actions-Preventive Actions (CAPA)
  •          Risk Assessment
  •          Supplier (Vendor) Qualification

 

 

 

 

We will support the company’s capability to produce product per customer requirements by setting up Quality Management Systems for Chemical, Pharmaceutical, or Medical Devices companies.

We will assist you with documentation preparation, monitoring quality, training, audits, and preparation for ISO certification.

 

        

 

 

 

We will assist you with establishing your monitoring processes.

Monitoring Quality is performed by using all or some of the following:

1. Statistical   methods

    • Control Charts

    • Ishikawa Diagrams

    • Pareto Diagrams

    • Scatter Diagrams

    • Process capability

2.  Audits  

 

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We are committed to supporting companies to produce product per customer requirements by implementing the Quality Management System (QMS).

We will assist with documentation preparation, monitoring quality, training, audits, and preparation for ISO certification.

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