Packaging Validation: Regulatory Expectations & Risk Prevention

About this webinar

Ensuring packaging systems remain compliant, reliable, and fit for purpose throughout a product’s lifecycle is a key challenge for manufacturers operating in regulated industries. 

This webinar provides a clear overview of the critical considerations for developing robust packaging validation programmes, helping organisations meet global regulatory expectations while safeguarding product quality and patient safety. 

Join our experts as they explore the key elements of packaging validation, including aging studies, transport simulation, and packaging process validation. You will also gain practical guidance on identifying and mitigating risks early, enabling efficient and right-first-time validation outcomes. 

WEBINAR DETAILS

Date: Tuesday, 7^th July 2026 
Time: 3.30 pm IST 
Duration: 1 hour 
Language: English 
Speaker: Mr. Krishna Chaithanya Gubbilla, TÜV SÜD Expert 

Register Now

You will receive the access link by email after registration. 

WHAT YOU’LL GAIN FROM THIS WEBINAR 

• Packaging validation overview: Understand the scope, key objectives, and lifecycle approach to packaging validation
• Regulatory expectations: Learn about global requirements and how they apply to packaging systems
• Aging, transport and process validation: Gain insights into key validation activities and their impact on product quality
• Common challenges and risks: Identify typical failure points and how to mitigate them early in the validation process
• Achieving compliant outcomes: Discover practical approaches to improve validation efficiency and ensure right-first-time results 

WHO SHOULD ATTEND?

• Medical device manufacturers
• Consultants
• Medical-grade packaging material suppliers
• Regulatory and quality managers 

ABOUT THE SPEAKER

Mr. Krishna Chaithanya Gubbilla 
Expert, Sterilisation & Packaging, TÜV SÜD 

Krishna Chaithanya is a medical device quality, sterilisation, and packaging specialist with over 10 years of experience across manufacturing, quality assurance, regulatory affairs, and conformity assessment. 

He currently serves as a technical expert with TÜV SÜD, where he conducts assessments of technical documentation and conformity evaluations for medical devices, with a focus on sterilisation and packaging requirements under EU MDR 2017/745. 

Krishna has supported the certification and registration of medical devices across multiple global markets and has worked with a wide range of device classes and therapeutic areas. He holds a Master of Pharmacy (M. Pharm) degree and is a TÜV SÜD Certified Internal Auditor for ISO 13485.