This ISO/IEC 17025 lead auditor training course provides comprehensive training and certification to become a lead auditor for Laboratory Management Systems. The course includes lectures, handouts, an audit checklist, and exams.
DurationThis ISO/IEC 17025 lead auditor training course provides comprehensive training and certification to become a lead auditor for Laboratory Management Systems. The course includes lectures, handouts, an audit checklist, and exams. Delivered online, it allows busy laboratory technical team members to participate from anywhere at their convenience.
Participants will gain knowledge and understanding of various audit activities, including Audit Techniques, Audit Processes, and Audit Requirements according to ISO 19011:2018. The course covers how to conduct opening and closing meetings, and perform external audits in any organization. This thorough training will help laboratory employees and certifying body auditors qualify as Lead Auditors for Laboratory Management Systems based on ISO/IEC 17025:2017 and earn their lead auditor certification.
This course is invaluable for new assessors and serves as an excellent refresher for experienced assessors of ISO/IEC 17025. Consultants assisting clients in transitioning from other ISO standards or from the 2005 version to the latest ISO/IEC 17025 requirements will also find this course highly beneficial. Upon successful completion, participants will receive a certificate as trained ISO/IEC 17025:2017 Lead Auditors.
This course will enable you to:
Get acquainted with the high-level structure and framework of the laboratory management system.
Comprehend the clauses and sub-clauses of ISO/IEC 17025:2017 requirements.
Grasp organizational issues and the context of the organization.
Learn about leadership, planning, and support clauses.
Gain knowledge of technical requirements in testing and calibration laboratories.
Understand the operation and performance evaluation clauses.
Learn how to achieve improvements in the laboratory and audit with real-time examples.
Maintain and retain documented information lists.
Acquire knowledge of external auditing and the use of audit checklists.
Understand the auditing processes, including opening and closing meetings, and the requirements of ISO 19011 for auditing management system standards.
Familiarize yourself with ISO/IEC 17025:2017 Laboratory Accreditation principles
Understand the Plan-Do-Check-Act cycle of standard requirements.
Institute of Good Manufacturing Practices India, registered under SR Act XXI of 1860, Government of India, recognised by Ministry of Commerce & Industry, accredited Vocational Institution of Ministry of Education, Government of India and approved by Food Safety and Standards Authority of India (FSSAI) presents unique, friendly and interactive platform to get rid of all your GMP compliance related issues. GMP- an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing - in itself is the most dynamic part which witnesses frequent changes in terms of newer rules being added and older ones being renewed. Keeping self updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices.
Our group of learned professionals from above mentioned sectors of the Pharma, Healthcare, Food & Nutraceutical industries have put together their knowledge; know about and practical experiences in form of this GMP guide.
IGMPI is moving hand in hand with technology advances and has gained recognition as a stronger and better education and training platform provider for professionals and students in the areas of GMP, Quality Assurance and Control, Pharma, Food & Nutrition and Healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management.
The importance of quality healthcare and foods is known to our board of governors and thus numerous efforts are being made to offer friendly but effective and easy regular and online sources of GMP training,
Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice in form of formal classroom studies, online/interactive programmes, online seminars, as well as onsite training programmes along with knowledge of worldwide affairs of the industry;
in short a round-the-clock help for any information in these areas needed by anybody from around the country and abroad. Based on high standard of quality, the training programmes in Pharma, Healthcare and Food GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management, Public Health, Hospital Management, Clinical Research, Pharmacovigilance, Medical Writing, Medical Coding, Nanotechnology, Drug Design and Discovery, Food QA&QC etc areas have been approved by Quality Council of India, which is an autonomous body and an accreditation authority for education & vocational training providers under the Ministry of Commerce & Industry,
Government of India. IGMPI is duly licensed and certified by Bureau of Indian Standards (BIS) under Bureau of Indian Standards (Conformity Assessment) Regulations 2018.
The IGMPI's team of technology experts and other Industry advisors together pursue to make cGMP knowledge, training in the area of Pharma and Food manufacturing easily accessible, through this platform.
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