Commercialization Drug Device Combination Product

This webinar covers the commercialization of Drug-Device Combination Devices in healthcare, providing a roadmap for professionals in manufacturing, quality engineering, product development, and quality assurance.
Wednesday, January 29, 2025
Time: 10:00 AM PST | 01:00 PM EST
Duration: 60 Minutes
IMG Chaitanya Baliga
Id: 90068
Live
Session
$119.00
Single Attendee
$249.00
Group Attendees
Recorded
Session
$159.00
Single Attendee
$359.00
Group Attendees
Combo
Live+Recorded
$249.00
Single Attendee
$549.00
Group Attendees

Overview:

Prepare participants to better understand the a road map and consideration based on principles in medical device development with principles behind using Quality by Design to develop a pharmaceutical product. The webinar will focus on such a roadmap for a successful commercialization.

Why you should Attend:

The Drug - Device Combination Devices is a rapidly growing sector that plays a crucial role in healthcare. Innovation is at the heart of this industry, with companies constantly striving to develop new and improved devices to meet the evolving needs of patients and healthcare professionals. Commercialization typically begins at the end of clinical tests. At its essence, commercialization is the process by which companies find commercial methods for producing a product and then bringing that product to the market. This webinar provided a roadmap to successful commercialization of such products.

Areas Covered in the Session:

Commercialization of Dug Device Combination Product:

  • Clinical Stage
  • Regulatory pathway
  • Product Development stages using medical device and drug development approach
  • Quality Assurance Standards

Who Will Benefit:

  • Manufacturing Engineer and quality engineer with intermediate level experience in manufacturing, engineering and product development in medical and pharmaceutical industry
  • Technology transfer 
  • Product development scientist and engineers
  • Technical Operational Specialist/Lead
  • Technology Transfer Leads/Manager and MSAT professionals
  • Operational Excellence

Speaker Profile

Dr. Chaitanya Baliga has over 20 years of experience in quality management systems, regulatory compliance, and supplier management in industries, such as consumer products, medical device, pharmaceuticals, automotive, and toys. One of Chaitanya’s responsibilities is ensuring quality and compliance activities pertaining to manufacturing of regulated products (drugs, natural health products, cosmetics, and medical devices).