Pharma Best Practices Webinar

Pharma Best Practices Webinar

Qualification and Validation principles to meet revised schedule M requirements.

Register Here : Click here to Register for the webinar

About the Webinar

The Webinar will provide the objective and scope to detail the basic principles of qualification and validation, that can be applied to equipment, utilities, facilities and software within the life sciences industry. The qualification and validation principles are based on a lifecycle approach with the application of risk management principles.

The webinar will discuss the following topics broadly.


  1. The current Regulatory expectations on delivering a typical project.
  2. Basic principles of Lifecycle Management and the distinct phases.
  3. Development of governance documents and Quality Management Systems
  4. Implementation of a Science-based and Risk-based approach to the project\
  5. Stay focused on Product Quality and Patient Safety
  6. Requirements for Commissioning, Qualification & Validation activities.
  7. Requirements for acceptance & release and continuous improvement


About the Speaker

Sundar Chellamani is Founder and Director, Plimco Limited Ireland. Sundar has a master’s in engineering and a certificate in Pharmaceutical Auditing. He is a highly capable hands-on Technical Engineer and Project Manager with more than 30 years of international experience in various senior roles specialising in Lifecycle Management and C&Q in countries such as Singapore, China, Poland, India and Russia with global companies such as Merck, Viatris and Pfizer.

March 8, 2024 from 3.00 to 5.00 pm

About Pharma Best Practices Webinars:

This neutral and scientific platform was launched in March 2020 with mission to share knowledge without any commercial considerations for the benefit of Pharma Professional. A platform where any Subject Matter Expert from any Organisation – a Manufacturing organisation , a consulting firm, a Not for profit organisation like ISPE , PDA,ECA or IPA, regulator or a Manufacturer of equipment is invited and is welcome to present the latest in Pharmaceutical Technology , Quality and regulations.

A big thank you and our gratitude to all the Subject Matter Experts who wholeheartedly? supported us by presenting the latest knowledge in their respective fields on this platform in the last three years. Since the launch of this platform in the year 2020 ?we have hosted more than 125 educational sessions. About 40,000 professionals have attended live and another 150,000 professionals have watched recordings of the presentations.? Thank you for your trust and faith in us.

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