Seminar · San Francisco, California

2-day In-person Seminar on “Combination Products

Medicine · Pharmaceuticals

Official website
Next editionNot confirmedLast edition we have: 30–31 Oct 2014
Last venueCourtyard San Francisco AirportSan Francisco, California
RunningSince 2014Frequency unknown · 1 edition on record
Last checked12 Nov 2026Organiser website checked
We haven't confirmed the next dates yet. The last edition in our records was 30–31 Oct 2014 at Courtyard San Francisco Airport. Check the organiser's site: globalcompliancepanel.com. Are you the organiser? Correct this listing.

Key numbers

Editions on record
1first in 2014

About 2-day In-person Seminar on “Combination Products

Summary of the workshop:

This course provides a comprehensive understanding of the FDA Combination Product system. Participants receive a foundation of knowledge about the FDA Office of Combination Products, the FDA Combination Product system, Combination Product submissions, and the scientific and regulatory principles involved.

Participants will learn what a Combination Product is, learn about mode of action and primary mode of action, how to prepare a Request for Designation submission, Combination Product user fees, GMP for Combination Products and how to interact with the FDA Office of Combination products. They will also learn about submissions for post-approval modifications for a Combination product. This course provides the participant the ability to understand the entire FDA Combination Product Process and how to navigate through the FDA Combination Product Process to get your Combination Product onto the US marketplace.

Learning Objectives from this Workshop:

Learn about the FDA Office of Combination products

Learn what a Combination Product is

Learn the FDA Combination Product Process

How to navigate the FDA Combination Product system

Mode of action and primary mode of action

How to prepare a Request for Designation

User Fees for Combination products

GMPs for Combination products

Post-Approval Modifications

Meet your Expert:

Albert A. Ghignone, MS, RAC is the CEO of AAG Incorporated. For more than 30 years his focus has been on FDA related matters in regulatory affairs, quality assurance and clinical affairs. He has expertise in dealing with all aspects of the FDA approval process for drugs, biologics, medical devices and generic drugs. He has worked in every major segment of the industry-research, quality assurance, regulatory affairs, manufacturing and clinical.

From our listing of this edition. Details may have changed since.

Editions

YearDatesWhereExhibitorsVisitors
201430–31 Oct 2014Courtyard San Francisco Airport
San Francisco, California
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Past editions from the bvents archive (2008–2019) and organiser figures where they were published.

Questions

When is 2-day In-person Seminar on “Combination Products?

The next dates haven't been confirmed. The last edition we have on record was 30–31 Oct 2014.

Where is it held?

The last edition we have was at Courtyard San Francisco Airport, San Francisco, California.

Who organises it?

Global Compliance Panel.

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