ISO 22301 – What Global manager group’s Readymade ISO 22301 documents provide?

The ISO 22301 standard is written by leading business continuity experts and provides the best framework for managing business continuity in an organization. The ISO 22301:2012 is an international standard published by the International Organization for Standardization (ISO), and it describes how to manage business continuity in an organization.

The ISO 22301:2012, which was developed based on the British standard BS 25999-2. The ISO 22301:2012 standard definitely brings more flexibility and less prescriptiveness, adding more value to organizations and their customers. One of the features that differentiate this ISO 22301 standard from other business continuity standards is that an organization can become certified by an accredited certification body, and will therefore be able to prove its compliance to its customers and other stakeholders.

The main focus of ISO 22301 is to ensure continuity of business delivery of products and services after occurrence of disruptive events. The implementation of ISO 22301 will involve not only setting organizational rules that are needed in order to prevent disruptive incidents, but also developing plans and allocating technical and other resources to make the continuity and recovery of possible business activities. ISO 22301 has described how to fit all these elements together in the Business Continuity Management System (BCMS).

An ISO 22301 certification helps organizations implement a BCMS that meet the requirements of the organization, taking into account the legal, regulatory, and industry requirements, as well as the products, services, and processes established in the organization. In addition, the ISO 22301:2012 standard is used to mitigate and control the risks of exposure to internal and external threats, ensuring organizations can effectively respond to security incidents, data breaches, and more.

The initial implementation of an ISO 22301 will require a significant amount of resources such as time and effort in preparation of their ISO 22301 documentation. With that in mind, Global Manager Group has developed ISO 22301 Documentation Kit based on requirements of ISO 22301:2012 standard which includes following readymade templates that can be used as a ready reference tool to accelerate documentation process for BCMS certification.

Which readymade documents are covered in this ISO 22301 documentation Kit?

• ISO 22301 Manual 
• BCMS Procedures
• Exhibits
• Standard Operating Procedures
• Readymade Formats
• Job Description
• ISO 22301 Audit Checklists

Global Manager Group is involved in documentation selling since 1995; here, The ISO 22301 documentation kit is one of the most selling document products of the company. The aim and purpose of providing readymade ISO 22301 documents is to help organization in integration of Business continuity management system for easier management and operations.

The ISO 22301 Documentation kit for Business continuity management system developed by Global Manager Group is consistent in its appearance, and is written and reviewed by recognized authorities in the area. User can also receive support and guidance on using this documentation toolkit. The ISO 22301 documentation kit can also help to understand the management system requirements and make proactive changes to any workflows. By saving time, GMG’s toolkits allows to focus more on ensuring that the necessary processes and procedures are performed and disseminated throughout the organization.

What are the requirements of ISO 17025:2017 for laboratory measurement equipment and related procedures?

Implementation of the ISO/IEC 17025 standard, Laboratory accreditation is obtained through the process that determines the competence of laboratories to provide accurate results. At the global level, with the economic crisis, manufacturers and suppliers must reduce their operating costs. To be able to meet that ISO 17025:2017 requirement, modern laboratories must use the ISO 17025 for high-quality measuring equipment.

To obtain the correct measurement result for equipment, the laboratory must employ an organized approach in the measurement process. As per the ISO 17025:2017 standard’s requirements state that laboratories must demonstrate their competence, practical work requires the proper use of laboratory equipment and commits to following controlled procedures.

Here, the topic highlights the large number of activities that could influence a measurement result. For any testing laboratories you wish to be ISO 17025 accredited for, the starting point is to map the processes and activities related to the measurement test. So, Following are the risks and determine controls that should be placed: 

• Management of personnel competency
• Document control of procedures
• Effective technical records
• Suitable facilities and conditions
• Suitable calibrated equipment
• Certified reference materials
• Suitable reagents
• Suitable test method
• Validated methods
• Correct handling of samples

According to the standard, ISO/IEC 17025, The main tools for work in a laboratory are known as laboratory equipment. Laboratory equipment may include the main measurement instruments, measurement software, auxiliary measurement modules and equipment, reagents, consumables, and certified reference materials needed for the correct performance of the measurement procedure.

There is not all measurement equipment ensures success in the laboratory. With the competence of associated clauses, the laboratory must provide proof that it uses uniquely identified and calibrated equipment, that this equipment is in the correct state and that it is regularly tested and maintained and, of course, that it provides skilled personnel to operate that equipment.

Laboratory equipment is influenced by the place where the measurement is performed and its valid use. For the laboratory premises, Measurement can be done, where environmental conditions are controlled and it is easier to maintain repeatability for any consecutive measurement. But, in some of conditions, measurements must be performed onsite, where environmental conditions are different and may influence the validity of the measurement.

In any case, for the laboratory’s reputation to be preserved, it is necessary to use auxiliary measurement equipment to monitor, control, and record environmental conditions. The quality of the measurement equipment must be maintained through following procedures for use of the laboratory equipment.

Those ISO 17025 procedures must define and continuously provide information about the “health” / suitability of the measurement equipment which including:

• Proper methods of handling
• Proper methods of transport in the case of on-site measurement, service repairs, proficiency testing (inter-comparisons), or recalibration
• Proper methods for handling of equipment during measurement, maintenance, or storage by the laboratory personnel
• Regular and repeatable testing of equipment for basic verification checks that equipment can achieve the measurement accuracy and/or measurement uncertainty required to provide a valid result
• Tracking of laboratory equipment age and possible physical damage, firmware version updates, or software failure
• For detailing equipment usage provision of records, repair, proficiency testing, recalibration, etc.

The audits done by certification firms ensure that the businesses square measure in compliance with the ISO standards or not. The professionals from the businesses assess and valuate the corporate policies, practices and ISO 17025:2017 documents procedures. The ISO 17025 certification involves many alternative processes all levels of labor in among the corporate.

A Guide to BRC Global Standard for Consumer Product

The BRC Standard for Consumer products was first published in 2003 and developed by the British Retail Consortium (BRC), the BRC Global Standards outline requirements imposed by British retailers for a range of products – with the aim of ensuring safety, legality, and quality of products.

And since then it has undergone extensive changes to support the needs of the wide-reaching consumer products industries. Along the way it has developed into a robust Standard based on the principles of risk assessment and good manufacturing practice to deliver safe, legal products of specified quality to the end-consumer.

This BRC standard focuses upon the identification and management of risks and the implementation of preventive measures, with hygiene as a central element of the quality management system (QMS).Basically, the scope of the Global standard of BRC Consumer Products, Issue 3 mainly covers a wide range of non-food products in the global marketplace; including formulated products such as shampoos, paints and cosmetics, etc. and the non-food products may be retailer brands or national brands.

Meeting those BRC Global standards is mission critical for your business, since the majority of UK – as well as many European and global – retailers and brand owners only consider with doing business with suppliers who have gained BRC Consumer products certification of the appropriate BRC Global Standard.

BRC Consumer product certified against this standard to demonstrate their competence in maintaining product safety, legality and integrity for manufacturing and assembly packing companies. The written to address the requirements for BRC Global Standard for consumer product has been in relation to   potential of the product to cause harm to the Consumer.

Requirements for BRC Global Standard Consumer Products 

Following are four different sets of requirements for BRC Global Standard Consumer Products defines for the different product groups. The requirement differentiates between the product groups, but always covers the following topics:

• Product risk management
• Consumer product management system
• Site environmental standards
• Product control
• Process control
• Personnel

Advantages of the BRC Consumer Products Certification

• Stabilize the customer confidence
• Stabilize product safety, -quality and -legality in trading companies
• Security of Higher product 
• Lower product liability risks
• In the sense of product security and steering of processes, Systematic analysis, implementation of safe and more efficient process cycles 
• Timely notice of consumer risks concerning hygiene and security of consumer goods. And Define of appropriate preventive measures.

For ready reference which Contains document template and you could possibly need (both mandatory and optional), as well as additional work instructions, project tools and documentation structure guidance, Global manager group’s BRC consumer product documentation kit really is the most comprehensive option on the market for completing your documentation. The BRC Consumer Products Documents conforming to the requirements of the standard.

Source: foodsafetystandard.wordpress.com