Regulation of Combination Products

Early Registration Discount
Early registration until June 7, 2020
3,330 NIS + VAT
Registration from June 8, 2020
3,700 NIS + VAT
Lecturer: Dr. Sara Horn

Date: TBA
Location: Kfar Maccabiah, Ramat Gan
General Information
Duration: 1 - Day Course
Hours: 09:00-17:00
Price: 3,700 NIS + VAT
Credit Points: 1
SKU: 20432
Course Language: Hebrew
About the Course
The field of combination products is dynamic and is constantly growing and developing in the world and within Israel as well. This field include products made of a combination of different components (such as device, biologics or and/or drugs). The regulatory requirements in this field are getting more and more complex and raise new standards and challenges, due to the complexity of these products.

Being these combination products, the development pathways to be used may be different  and the strategy chosen might lead to a different outcome in terms of product requirements and time to market. The regulatory strategy to be selected is therefore particularly critical for the success of the development of these types of product.

The course is aimed to provide an overview of the current regulatory guidelines in this field. The course provides information about the life cycle of these products and different regulatory approach for biological products, pharmaceuticals and medical devices and focuses on the possible approaches for these type of products.
Who should attend
  • Quality assurance and regulatory affairs managers and experts
  • Project managers dealing with combination products
  • Managers in start-up companies dealing with combination products
Regulation of Combination Products
Benefits to the Participants
Knowledge of the regulatory bodies that shape this emerging field. Understanding of the main differences in the regulatory requirements of different types of products (device/biologics/drugs). Evaluation of the possible different regulatory approaches and understanding of the processes for a successful product development for these product types.  Understanding of the differences in the approaches in US and in EU.
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Issues to be covered
  • Introduction
    • The history behind the need for combination product regulations
    • Definitions
    • Differences between drugs/biologics and devices
  • The regulatory process
    • Primary mode of action
    • FDA OCP
    • RFD content
    • Jurisdiction process
    • Meetings with RA bodies
  • Development of combination products
    • Non clinical
    • Manufacturing
    • Clinical
    • Meetings with RA bodies
    • evelopment considerations
  • Products classification and RA strategies
    • Combination product types and product classification
    • Regulatory challenges and strategy
  • Downstream issues
    • Quality systems and cGMP for combination products
    • Post Approval modifications
    • Post marketing safety reporting
  • Borderline products in EU
    • Regulatory bodies/processes
    • Products classification
  • Case studies
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