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KE MRI STANDARD OPERATING PROCEDURE FOR INTERNAL QUALITY AUDITS ISSUE NUMBER 02 ISSUE DATE 7TH NOVEMBER 2012 REVISION STATUS 01 REVISION DATE 18TH OCT0BER, 2012 KENYA MEDICAL RESEARCH INSTITUTE DOCUMENT
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Point by point instructions on how to fill out the ISO manual - KEMRI:

01
Begin by familiarizing yourself with the ISO manual requirements specific to KEMRI (Kenya Medical Research Institute). This will ensure you understand the guidelines and standards set forth by ISO for KEMRI.
02
Gather all the necessary information and documentation that is required to complete the ISO manual. This may include KEMRI policies, procedures, and other relevant materials.
03
Start by creating a table of contents for the ISO manual. This will help organize the different sections and make reference easier for users.
04
Divide the ISO manual into sections pertaining to different aspects of KEMRI's operations. This could include sections on quality management, risk management, documentation control, training and competence, etc.
05
For each section, outline the necessary information and procedures that need to be included. This can include documenting processes, identifying roles and responsibilities, ensuring compliance with ISO standards, and incorporating any specific requirements of KEMRI.
06
Provide clear and concise instructions within each section, ensuring that the information is easy to understand and follow.
07
Include relevant forms, templates, and checklists within the ISO manual to assist users in implementing the procedures. These can be used to record information, track progress, and ensure compliance.
08
Regularly review and update the ISO manual as needed. This will help ensure that it remains current and aligned with any changes in ISO requirements or KEMRI's operations.

Who needs the ISO manual - KEMRI?

01
Organizations and individuals involved in KEMRI's operations who are seeking ISO certification or compliance.
02
Quality managers, supervisors, and employees responsible for implementing and following ISO standards within KEMRI.
03
Auditors and inspectors who assess KEMRI's conformity to ISO requirements.
04
External stakeholders, such as partners, clients, and funding agencies who require assurance of KEMRI's adherence to ISO standards.
05
Anyone interested in understanding KEMRI's quality management system and processes, including researchers, healthcare professionals, and policymakers.
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The ISO manual for KEMRI is a document that outlines the quality management system of the Kenya Medical Research Institute.
All departments and units within KEMRI are required to file the ISO manual.
To fill out the ISO manual for KEMRI, departments and units should follow the guidelines provided in the quality management system.
The purpose of the ISO manual for KEMRI is to ensure that the organization meets the requirements of international quality standards.
The ISO manual for KEMRI should include information on the quality objectives, processes, and procedures within the organization.
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