Awareness Program on Clean Room & Biocontamination Control

Awareness Program on Clean Room & Biocontamination Control

Feature:

This course is designed to meet the requirement of competent auditors referred in ISO 19011. The course includes class room sessions coupled with syndicate group exercises to enhance delegate participation to achieve learning objectives. Medical Devices - Quality Management System that can be used by an organization involved in one or more stages of the life-cycle of a medical device, including design and development, production, storage and distribution, installation, servicing and final decommissioning and disposal of medical devices, and design and development, or provision of associated activities (e.g. technical support).

Course Objectives

To enable delegates understand Key concepts in Clean Room & Biocontamination Control


Date and Time

Date : 17th to 19th and 25th to 26th October 2024

Time : 9:00 AM to 6:00 PM

Who should attend ?

Generally anyone involved in Medical Devices Industry but specifically:

  • Quality executives/managers
  • R& D Personnel
  • Regulatory Affairs personnel
  • Management representatives
  • QMS Consultants
  • MD Importers
  • MD Software developers/validators
  • Personnel wishing to attend higher level courses such as Lead Auditor courses.

 

Prerequisite/Prior knowledge
  • Introduction to Medical Device, 
  • What’s New - Introduction to EU MDR
  • Main Articles and Annexes 
  • Scope
  • New or Modified Definition 
  • Clinical Evaluation consultation and Mechanism of Scrutiny
  • Summary Of Safety and Clinical Performance 
  • General Safety and Performance
  • Enforcements Dated – Interpretation of Article 120 and 123 
  • Implementing acts 
Course Contents
  • ISO Cleanroom classifications and specifications
  • Alignment with ISO 13485 and ISO 14971 and Regulations
  • Understanding ISO 14644 and EN 17141:2020 Biocontamination control requirements
  • EN 17141-2020 Informative references (Annex B, E and F)
  • Brief overview of ISO 13408 standard on Aseptic processing of health care products
Certificate

Certificate of successful completion shall be issued to all the delegates who attend entire duration of the course and pass the online exam.

 

Duration

8 Hours including a break of 1 hour for both days

Registration Fees

Rs. 32,000/- + 18 % GST Only

Registration and Payment

https://pay.tuv-india.com/index1.php?mtid=9189514

Registration with confirmed payment will be closed 24 Hours before the scheduled time of Webinar.

 

Cancellation Policy

In case of change or cancellation of any scheduled program from TUV India Pvt. Ltd, fees paid for participation will be initiated for refund to the respective participant / client account within 21 days once required information is provided by participant / client.