Friday, June 19, 2020

Overview and Training Requirements for ISO 15189

ISO 15189 Accreditation is a guarantee that the laboratory has been tested by internationally recognized standards aimed at proving the availability of the program, the technical capacity, and that the staff actually has the ability to produce appropriate technical results and specific details for the purposes for which each test is used.

In order to comply with the requirements of ISO 15189, strong involvement of laboratory staff is required to understand the best process for satisfying the requirements according to the latest technology and methodology, scientific documents, but also time and cost. A growing number of voluntary medical are taking the path to approval, so ensure practice and technical competence in accordance with the Laboratories Best Practice policy, as well as boost confidence in laboratory tests by all participants, thus including patients and physicians.

The ISO 15189 Standard requires, in part, a document, to agree on the purpose for which each test is intended. For example, it instructs laboratory staff to evaluate the validity of the performance indicators of the test procedures and whether the limitations can be controlled by the lab, so that the adverse impact on patients' outcomes can be avoided.

Another important factor related to choosing the size of ISO 15189 is accreditation. Each test, independently of the environment or technology, can vary widely the patient's health and safety outcome. Therefore, accreditation of clinical laboratories should include the largest number of laboratory tests performed.

Proper training of laboratory staff is the first step in introducing accreditation. This clearly includes acknowledging the importance of laboratory medicine in health care and ensuring that the right results are given to doctors. However, continuous monitoring and monitoring of the entire process is needed to ensure consistency of the methods and procedures that should ensure the effective contribution of the test results to patient care.

The ISO 15189 Auditor Training, in which can understand the requirements for Quality and Competence in Medical Laboratories and to learn everything that an ISO 15189 certified auditor needs to aware about auditing a laboratory. First, all the ISO 15189 requirements are discussed in order to understand and accept the basis under approval. Treated as a workplace training exercise, is where all employees are involved in a professional forum by saying the following:
  1. Read and interpret all requirements and concurrent negotiations of procedures, ensure compliance of requirements and in accordance with revised and approved guidelines;
  2. Collection of proposals for improving the level of compliance and assessment accordingly and feasible;
  3. Exploring new approaches and / or processes, and introducing alternatives.

The Accreditation Body plays an important role in teaching and training the auditors correctly. Training needs to focus on the processes and procedures of the audit but, first of all, how to emphasize the quality of the lab, not only in terms of requirements, but also in relation to improvement programs and projects, which should be clearly recognized as an additional value. For getting ISO 15189 Accreditation Consultancy services please visit: http://www.accreditationconsultancy.com/iso-15189-accreditation-consultancy.htm

Thursday, June 11, 2020

Introduced ISO 17020:2012 Document Template Online at Accreditationconsultancy.com

Accreditationconsultancy.com, website that aims to share information and knowledge regarding all ISO/IEC accreditation standards has introduced Ready to use ISO 17020:2012 Documentation Template online. The ISO 17020 document kit will be useful as key guide and readymade solution for conformity assessment inspection body certification documentation process.

After help of experienced team of consultants and auditor in preparation of ISO 17020:2012 documentation, this product has been ready and introduced to global market on website to comply with ISO 17020:2012 Standard. ISO/IEC 17020 documents templates will guide user to easily create fast and effective conformity assessment for inspection body. The ISO 17020 documents product offered online has covered all the requirements as per ISO 17020:2012 standard, which includes ISO 17020:2012 manual, procedures, exhibits, SOP, ISO 17020:2012 audit checklists etc.

Organization has short of time and do not want to spend their entire time in documenting task. Accreditationconsultancy.com has introduced ISO 17020 Documents to help such people by delivering accurate information and reference documents required for ISO 17020:2012 that minimize Clients' time and results quick certification.

The ready to use ISO 17020:2012 Documents priced at 450 USD, which covers sample templates that are written in simple English and easily editable format. The user can update total documentation templates as per organization working system and create own documents for their company in quick time.


About www.Accreditationconsultancy.com

Accreditationconsultancy.com is provider of ISO/IEC accreditation solutions online, which is owned by Global Manager Group. The company delivers benefits to laboratories or organization by providing information about all ISO Accreditation Standards. Company has team of expert consultants having rich experience of implementing various international system certification and / or documentation that works with their customers to reduce cost and save time in implementing the system. The website offers a wide range of certification solutions for ISO 17020, ISO 17021, ISO 17024, ISO 17025, ISO 17034, ISO 17043, ISO 17065, ISO 15189 and more. To know more about the documentation and company's online consultancy services visit website at www.accreditationconsultancy.com