'Document control' diaporamas de présentation

From Good Laboratory Practice to Total Quality Management in Medical Laboratories : The Perspective

From Good Laboratory Practice to Total Quality Management in Medical Laboratories : The Perspective. October, 2002 S Cheng. What is Quality. Quality is the entity of a product ( service ) which fulfils the defined and expected requirement

2.55k views • 70 slides

The ISO 9000 Standards for Quality Management Systems

827 views • 56 slides

HACC National Service Standards

HACC National Service Standards. Educational Manual. Purpose of the Educational Manual. The purpose of the educational manual is to assist HACC Service Providers to develop the systems and processes required to meet three of the HACC National Service Standards, namely:

617 views • 44 slides

5.2 Personnel

5.2 Personnel. Use competent staff Supervise as necessary Document qualifications and training Maintain documented training program Define responsibilities and authorities Applies also to contracted workers. 5.3 Accommodation, Environment. Accommodation & environment to suit testing

492 views • 34 slides

Non-conformances / Document Control

Non-conformances / Document Control. Dr A A Khine Chemical Pathology NHLS TYGERBERG Lab Management Workshop June 4-6 2019. Non-conformance in medical laboratory. A failure to conform to accepted standards or SOP

856 views • 33 slides

Topic 4 Environmental Management Systems

Topic 4 Environmental Management Systems. Chapter 32. The Concept. So, what exactly are they?. Developing an EMS. Create an environmental policy Set objectives and targets Implement a program to achieve objectives Monitor and measure its effectiveness Correct problems

313 views • 31 slides

Environmental Management System 14001:2004

Environmental Management System 14001:2004 . Presented By: Paras Sharma Rahul Gossain Suneet Sharma Varun Sharma Nilesh Baid. Registration Process. Becoming ISO 14001 registered. The registration body examines EMS for conformity to the ISO 14001 standard.

619 views • 29 slides

NCS International

440 views • 28 slides

Quality Manual Structure and Contents

Quality Manual Structure and Contents. Quality Manual Structure and Contents - optional. Organization. Personnel. Equipment. Process Control. Purchasing & Inventory. Information Management. Assessment. Documents & Records. Occurrence Management. Process Improvement.

385 views • 22 slides

Documentation system

Documentation system. Q-Policy statement. Q-manual. Procedures (SOPS). Instructions and forms . Document control -1 (ISO 17025: 2005,4.3). Laboratory shall establish and maintain procedures to control all documents of the management system

700 views • 20 slides

Documentation system

Documentation system. Q-Policy statement. Q-manual. Procedures (SOPS). Instructions and forms . Document control -1 (ISO 17025: 2005,4.3). Laboratory shall establish and maintain procedures to control all documents of the management system

629 views • 20 slides

Haldex Brake Products

607 views • 19 slides

Extending Our Reach Through Partnerships June 2-6, 2013 Phoenix, Arizona

Extending Our Reach Through Partnerships June 2-6, 2013 Phoenix, Arizona. Extending Our Reach Through Partnerships June 2-6, 2013 Phoenix, Arizona. Extending Our Reach Through Partnerships. June 2-6, 2013 Phoenix, Arizona. Overview.

241 views • 17 slides

Engineering Practices Working Group Accomplishments & Plans

425 views • 13 slides

Commercial Awareness for Project Managers

785 views • 11 slides

EMS Development Course for Government Agencies

255 views • 10 slides

What is ISO/IEC 17025 Accreditation?

Learn about ISO/IEC 17025 standard for testing and calibration laboratory management system and standard requirement of ISO/IEC 17025 certification. This presentation cove what is accreditation, benefits, documentation and more.

619 views • 10 slides

REQUIREMENTS FOR COMMISSIONING DOCUMENTATION

REQUIREMENTS FOR COMMISSIONING DOCUMENTATION. DOCUMENTATION RULES. Consistency Clarity Formatting File Management Document Control Distribution Protocols. DOCUMENT TYPES Administration Process Informational.

138 views • 5 slides

Global Process Flow Diagram

Global Process Flow Diagram. New Part or New Customer & Part. Existing Customer & Part, Order Received & Reviewed. Refer to customer. Contract, Review, Identify Feasibility. Reject. Order Raw Materials FMEA 10. Production Planning. Accept. Process Design . PC03b

1.04k views • 2 slides

What are we discussing?

136 views • 0 slides