Digital Training
Gain the in-demand skills & knowledge of International Standards Online
100% Passing Record
Training By Expert Faculty with Real-Time Industry Scenarios
Standard Certification
Validate your skills and enhance your credibility with an International Credential
Contact Us for the corporate training and certification process.
Key features
ISO Lead Auditor Training
5 Days Interactive trainer-led Online Classroom / Group Training.
Handouts and study materials are designed by subject matter experts for step by step understanding and practical approach for new and experienced candidates both
1. The (first day) course starts with familiarizing ISO Standard, Annexure, Handouts, etc.
2. The session starts with the ‘Doubt Clearing Session’ before moving to a new topic every day.
3. Daily sample tests get conducted at the end of each day for providing a concrete grip on concepts and the nature of questions for the final exam.
4. The core work of an auditor i.e. ‘NC Writing and Audit report writing’ takes place from the very third day under the supervision of a trainer to provide practical experience.
5. Session on Stage one audit/ Final audit/ surveillance audit/ Certification audit/ Re- Certification audit.
6. Practical session on Man days calculation based on the size of the organization.
7. The trainer gives the training in the above mentioned scientific way to ensure what you read at the beginning of class is understood clearly by you; doubts are cleared every day, every day you write the sample paper – exam with absolute clarity so that during the final exam you have clear concepts about the Standard. The session is designed on the basis of real-time experience from different sectors.
Highly qualified, expert & accredited trainer with vast experience who is associated with the Bureau of Indian Standard (BIS). He is a very efficient and effective trainer for the ISO standards (like ISO 9001/37001/27001/22301/45001 etc.) with vast experience of training delivery to foreign delegates too.
We provide:
Convenient Weekday/Weekend ISO training online.
Support after the course completion/Doubt clearance during exams
Chance to speak to the trainer before registration of the course on-call:
+91 807-654-7619
Choose the perfect Certificate
Organizations need individuals with knowledge of international standards to help transform their business. Our training and certification helps you build, validate and enhance your skills with an International Credential
ISO 9001:2015 Quality Management System (QMS) is internationally recognized as the world’s leading quality management standard and has been implemented by over one million organizations in over 170 countries globally.
The purpose of the standard is to assist companies in meeting statutory and regulatory requirements relating to their product while achieving excellence in their customer service and delivery. The standard can be used throughout an organization to improve the performance or within a particular site, plant or department.
ISO 14001 Environmental Management System (EMS) is a systematic framework to manage the immediate and long term environmental impacts of an organization’s products, services and processes.
ISO 14001 environmental certification provides a framework for environmental management best practice to help organizations:
- Minimize their environmental footprint
- Diminish the risk of pollution incidents
- Provide operational improvements
- Ensure compliance with relevant environmental legislation, and
- Develop their business in a sustainable manner.
ISO 45001 is an International Standard that specifies requirements for an occupational health and safety (OH&S) management system, with guidance for its use, to enable an organisation to proactively improve its OH&S performance in preventing injury and ill-health. ISO 45001 is intended to be applicable to any organisation regardless of its size, type and nature.
Good manufacturing practice (GMP) is a concept that ensures products are consistently produced and controlled according to quality standards.It is designed to minimise the risks to the patient involved in any pharmaceutical production.
Its rules and interpretations differ from country to country and change frequently. Therefore, having fully trained experts at hand to help with the implementation of these rules is very important.
ISO 20000-1:2018
ISO 22000:2018
ISO/IEC 27001:2013
ISO 50001:2018
ISO 13485:2016
ISO 22301:2012
ISO 21001:2018
ISO 55001:2014
ISO 41001:2018
ISO 37001:2016
ISO 29990:2010
FSSC 22000
HACCP
GDP
ISO 39001:2012
ISO 21898:2004
ISO 27018:2014
ISO 10668:2010
CSN 01 0391:2013
ISO 10004:2018
ISO 10002:2018
GDPMD
ISO/TS 16949:2009
ISO 20121:2012
ISO 20000-1:2018
What we cover in our course?
1. Audit planning (Man Days calculation)
2. Audit interview Scenario
3. Managing an Audit Plan
4. Making Draft audit reports
5. Making Gap Assessment Report (Risk Register and Issue Tracker)
6. Drafting non-conformity reports
7. Drafting audit working documents
8. Documentation review (Stage 1 Audit)
9. Writing Non-conformity and doing follow-up actions
10. Session on leading a team of auditors as a Lead Auditor
11. One to one doubt clearance session
