2-day In-person Seminar

Combination Products Regulations: Drug and Device Combinations in the USA and EU


November 27th & 28th, 2017

Time: 9:00 AM to 5:00 PM

Zurich, Switzerland

Venue: Hilton Zurich Airport


Director : Salma Michor

**Please note the registration will be closed 2 days (48 Hours) prior to the date of the seminar.

  Price: $1,895.00
(Seminar Fee for One Delegate)

  Register for 5 attendees   Price: $5,685.00
      $9,475.00 You Save: $3,790.00 (40%)*

  Register for 10 attendees   Price: $10,422.00
      $18,950.00 You Save: $8,528.00 (45%)*
Course "Combination Products Regulations: Drug and Device Combinations in the USA and EU" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

This seminar provides Professionals working in this area with

  • A thorough understanding of the complexities involved
  • All the relevant regulations and guidelines
  • Real life examples of how to register and maintain various types of combination products
  • Interfaces: Change Management and LCM
  • Compliant safety reporting for combination products
  • Documentation requirements and interfacing

Why you should attend :

Combination products are especially challenging to register and maintain since they consist of two or more regulated components covered by different and usually independent sets of regulations in both the EU and US and various other regions.

Delegates working in this area must keep abreast of current and new legislation in this complex area to ensure a good regulatory strategy and compliance of their products.


Areas Covered in the Session:

Documentation requirements and interfacing
  • Documentation requirements for combination products EU
  • Documentation requirements for combination products US
  • Interfacing, development, quality, regulatory
  • Managing third parties and document control.

Who Will Benefit:

  • Regulatory Affairs
  • Medical Officers
  • Clinical Trial Managers

Day 1 Schedule


Lecture 1:

A high level overview to Combination Products

Including an interactive group session reviewing individual expectations
Lecture 2:

Introduction to Drug/Device Regulations

During this introductory session, delegates will gain a complete guide to the status and impact of the latest guidelines for combination products. Examples (company specific) of combination products will also be discussed to gain insights into their variety and complexities. Regulatory Requirements for: US and EU
Lecture 3:

CE Marking, 510 K and PMAs general Overview

  • US and EU
Life Cycle Management
  • Interfaces: Change Management
  • CTA applications
  • Annual reporting

Lecture 4:

CASE STUDY 1 - Including a walkthrough of expected outcomes for all case study exercises


Wrap up of day 1 & Q&A's

Day 2 Schedule


Lecture 1:

Overview Combination product Regulation and CTD dossier requirments: EU and US (A comparative review)


Lecture 2:

Clarifying the regulatory requirements of combination products and addressing life-cycle management

  • Examining the regulatory requirements for drug device combinations in the case of a drug and a device and for integral products
  • Annual reports
  • Case studies

Lecture 3:

CASE STUDY 2


Lecture 4:

Compliant safety reporting for combination products

  • Taking into account your product's combined components when addressing adverse event reporting
Documentation requirements and interfacing
  • Documentation requirements for combination products EU
  • Documentation requirements for combination products US
  • Interfacing, development, quality, regulatory
  • Managing third parties and document control.

CASE STUDY 3
Wrap up of day 2

Final Q&A & Summary of 'working smart' with Combination Products



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Group participations
Get fabulous discounts by participating in groups of two or more.
No Attendees Discount
1 2 Attendees 10% off
2 3 to 6 Attendees 20% off
3 7 to 10 Attendees 25% off
4 10+ Attendees 30% off

To avail the above group discounts, all the participants should register by making a single payment

Call our representative TODAY on 1800 447 9407 to have your seats confirmed!

Salma Michor

PhD, MSc, MBA, CMgr, RAC

Salma Michor is founder and CEO of Michor Consulting Schweiz GmbH, serving such clients as Johnson & Johnson, Novartis, Shire, Pfizer and Colgate Palmolive. Previously, Michor worked for Chiesi-Torrex, Wyeth Whitehall Export Croma Pharma GmbH. She teaches regulatory affairs and clinical strategies at the University of Krems, Austria, and is an independent expert to the European Commission. She holds a PhD in thermal process engineering and an MSc in food and biotechnology from the University of Applied Life Sciences in Vienna, Austria; an MSc from King's College, University of London in food technology; and an MBA from Open University, and has earned the RAC (EU), CQA and is a Chartered manager.

Location: Zurich, Switzerland Hotel: Hilton Zurich Airport   Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland. +41 44 828 50 50

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