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Combination Products Regulations Course | USA & EU Seminar 2018

From Tuesday, May, 15, 2018 to Wednesday, May, 16, 2018 in Zurich
Starting from:09:00
Concerned sectors: Biology -Biomedical -Biotechnology -
DESCRIPTION
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.
Overview:
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
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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.
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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.
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Who Will Benefit:
• Regulatory Affairs
• Medical Officers
• Clinical Trial Managers
Day 1 Schedule
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Lecture 1:
A high level overview to Combination Products
Including an interactive group session reviewing individual expectations
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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
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Lecture 3:
CE Marking, 510 K and PMAs general Overview
• US and EU
Life Cycle Management
• Interfaces: Change Management
• CTA applications
• Annual reporting
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Lecture 4:
CASE STUDY 1 - Including a walkthrough of expected outcomes for all case study exercises
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Wrap up of day 1 & Q&A's
Day 2 Schedule
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Lecture 1:
Overview Combination product Regulation and CTD dossier requirments: EU and US (A comparative review)
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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
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Lecture 3:
CASE STUDY 2
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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
Speaker
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 Date: May 15th & 16th, 2018 and Time: 9:00 AM to 5:00 PM
Venue:  Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland
Price:
Price: $1,695.00 (Seminar Fee for One Delegate)
Register for 5 attendees Price: $5,085.00 $8,475.00 You Save: $3,390.00 (40%)*
Register for 10 attendees Price: $9,322.00 $16,950.00 You Save: $7,628.00 (45%)*
Register now and save $200. (Early Bird)
Until April 10, Early Bird Price: $1,695.00 From April 11 to May 13, Regular Price: $1,895.00
Sponsorship Program benefits for “Combination Products Regulations: Drug and Device Combinations in the USA and EU” seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship 
Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com  
support@globalcompliancepanel.com 
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com

Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901483SEMINAR?SEO
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PUBLIC, SECTORS, ACCREDITATION
Accreditations: 0
Concerned Public: Professional
Attendance: International
Visitors/Participants: 50
Speakers: 1
Exhibitor: 1
Event Type: Colloquium
Major Sector: BIOLOGY
Concerned sectors: Biology -Biomedical -Biotechnology -
ORGANIZER / ADVERTISER

NETZEALOUS LLC - GLOBALCOMPLIANCEPANEL
161 Mission Falls Lane, Suite 216
94539 Fremont
UNITED STATES

COMMENT
REFERENCE
Congress, conferences or medical training REF #28-7976
Combination Products Regulations Course | USA & EU Seminar 2018
Published on congres-medical.com on:2018-04-05 11:11:49
Congress, conferences or medical training in BIOLOGY
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