Training

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Moments From Our Previous Sessions

Upcoming Training Sessions

ISO 13485:2016 (19th to 23rd May)

ISO 22000:2018 (19th to 22nd June)

ISO/IEC 17025:2017 (19th to 22nd July)

ISO 13485:2016 Medical Devices - Quality Management System

Fees: ₹29,999/-

₹ 14999 + GST

Who Should Attend?

1. Professionals involved in medical device design, production, installation, and servicing.
2. Organizations aiming to implement or maintain a Quality Management System (QMS) compliant with ISO 13485:2016.
3. Professionals seeking to enhance their understanding of medical device regulatory requirements and quality standards.

Key Takeaways

1. Comprehensive understanding of ISO 13485:2016 requirements and their application in the medical device industry.
2. Practical applications in real world scenarios.
3. A good learning experience from industry professional with over 35 years of experience.

Fees

₹14999 + GST only

ISO 22000:2018 Food safety management systems

Fees: ₹19999/-

₹ 4999 + GST

Who Should Attend?

1. Food safety managers, quality assurance professionals, and other enthusiastic individuals in food production, processing, and related fields.
2. Those who intend to apply for or are about to renew their ISO 22000 certification.
3. Any other person seeking more knowledge about the requirements of the ISO 22000 standard.

Key Takeaways

1. Gain a deep understanding of ISO 22000.
2. Practical applications in real world scenarios.
3. A good learning experience from industry professional with over 35 years of experience.

Fees

₹4999 + GST only

𝐈𝐒𝐎/𝐈𝐄𝐂 𝟏𝟕𝟎𝟐𝟓:𝟐𝟎𝟏𝟕

Fees: ₹19999/-

₹ 4999 + GST

Ensure your clean room operations meet the highest standards of performance and compliance with our focused online training on March 7, 2025, from 3 PM to 5 PM. This session is tailored to provide an in-depth understanding of clean room performance testing as per NABH Guidelines and ISO 14644.

What You'll Learn

Clean Room Performance Testing

Overview of clean room classifications under ISO 14644 standards.
Detailed guidance on clean room validation and performance testing requirements.
Compliance with NABH Guidelines

Understand NABH (National Accreditation Board for Hospitals & Healthcare Providers) clean room requirements for healthcare settings.
Learn how to align testing protocols with NABH standards for accreditation readiness.
Practical Insights

Key testing parameters: airflow, particle count, pressure differentials, and more.
Best practices for maintaining clean room performance.

Who Should Attend?

  • Laboratory supervisors, quality managers, and other enthusiastic professionals in calibration, testing and related fields.
  • Those who intend to apply or are about to renew their ISO/IEC 17025 certificates.
  • Any other person looking for more knowledge concerning the requirements of ISO/IEC 17025 standard.

Key Takeaways

  • Get deep understanding of ISO 17025.
  • Practical applications in real world scenarios.
  • A good learning experience from industry professional with over 35 years of experience.

Fees

₹4999 + GST only

Know Your Trainer

Mr. M.R. Sinha is a seasoned professional with over 35 years of experience in the calibration and testing industry. He has served as an NABL auditor, providing expert insights into quality assurance and compliance processes. Currently, he is the Director of Multitech Technofab Enterprises, where he leads initiatives in calibration, testing, and training.

With extensive experience in delivering training sessions for renowned organizations such as TATA Steel and Intertek, Mr. Sinha is well-versed in addressing critical topics in the industry. His expertise in uncertainty and decision rules ensures a practical and in-depth understanding of these essential concepts.

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