|
|
|
|
|
|
|
|
|
|
|
Table of Contents
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The European Compliance Academy (ECA) was founded on the
1st of January 1999 as an independent membership association and is today
the leading European association with regard to pharmaceutical Quality
Assurance and GMP compliance. Close to 4.000 members from all over Europe
and abroad represent more than 60 countries.
With the beginning of 2010 the organisation was transferred to a Foundation.
The purpose of ECA remains “the exchange of information between representatives
of the industry, the medicines authorities and the universities in the field of
pharmaceutical quality assurance, especially with regard to the area of Good
Manufacturing Practice (GMP).” It is comprised of a non-profit educational organisation
(ECA Academy) and various non-profit interest groups. The modern Foundation structure
allows to develop and include the activities of the interest groups and to have more
flexibility to build new interest groups that support the needs of our members.
The ECA Academy is an educational organisation managed in co-operation with Concept Heidelberg,
a professional conference organiser. Administrative tasks in this co-operation
like the organisational
handling of events and management of web services will be provided by Concept Heidelberg
since the ECA Foundation does not employ own staff. This new organisational structure and the
visualisation of the responsibilities provide the basis for a prosperous development of the organisation.
To learn more about the ECA please also see the ECA Image Folder
and the two videos about the services ECA provides and about social events at every course and conference.

For more information on the staff behind the ECA please see the organisation chart.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
"The ECA will provide support to the Pharmaceutical Industry and
Regulators to promote the move towards a harmonised set of GMP and
regulatory guidelines by providing information and interpretation of new or
updated guidances".
This includes among others:
- The development of the GMP Guideline Manager Software
with annual update
of all GMP-relevant regulations issued by the most important medicines
authorities and organisations worldwide
- Providing an Internet platform (www.gmp-compliance.org) for
research on and interpretation of the regulations regarding
pharmaceutical quality assurance and regulatory compliance
- The development of GMP tools aiming at the fulfilment of GMP
requirements defined by various regulatory authorities (e.g.
GMP Matrix)
- The organisation of education courses and conferences on
topical subjects concerning GMP and regulatory compliance.
All of the tasks are taken on by members, partners and the
Advisory Board.
With regard to the ECA’s goal to support the industry and authorities in promoting a harmonisation of GMP and regulations in Europe, the Academy initiated the European Qualified Person Association in 2006. QPs from all over Europe already signed up for a membership. You’ll find more information on this new group and its goals in the initial news and on the association’s website at
www.qp-association.eu.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
In order to do justice to the quickly-growing number of
members, on 15 July 2001 Dr Peter Reichelt, Managing Director of Reichelt
Chemietechnik, was appointed Chairman of the European Compliance Academy.
Starting from October 2005, Daniel Scheidegger, Vice President Operations
and Managing Director of Genzyme Pharmaceuticals Liestal, has been appointed
as the new ECA Chairman. The ECA Chairman is elected by the Advisory Board
for a period of 2 years. After this period, a new Chairman can be named, or
the same Chairman can be re-elected.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The ECA Advisory Board represents European regulatory authorities as well as the pharmaceutical and
biopharmaceutical industry. By their voluntary work, the board members
support ECA in fulfilling its mission to impart most relevant knowledge on
the interpretation and implementation of GMP and regulatory requirements.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The team focuses on the development of new courses and conferences on emerging GMP
challenges. The evaluation of all events by the Advisory Board ensures
best quality and participant satisfaction.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
So far it was only possible to become an ECA member through attending one of the ECA courses or conferences.
Since 2007 this has changed.
In addition to automatically becoming a member by participating in one of the European Compliance Academy courses or conferences marked with ECA (exception: Webinars) the Academy will offer two membership opportunities - an individual membership and a company membership.
Both will offer a whole range of benefits without requiring the attendance of a course or conference. To get more information, please read
here.
|
|
|
|
|
|
|
|
If you have any further questions regarding our organisation, please
contact us.
European Compliance Academy
P.O. Box 10 21 68, 69011 Heidelberg, Germany |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Many experts from European and US authorities as well as
from the industry already joined the team of ECA speakers and give regular
lectures during our courses and conferences. To learn more about the
benefits and how you qualify, please click here.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ECA's 1st Annual Review (1999)
ECA's 2nd Annual Review (2000)
ECA's 3rd Annual Review (2001)
ECA's 4th Annual Review (2002)
ECA's 5th Annual Review (2003)
ECA's 6th Annual Review (2004)
ECA's 7th Annual Review (2005)
ECA's 8th Annual Review (2006)
ECA's 9th Annual Review (2007)
ECA's 10th Annual Review (2008)
|
|
|
|
|
|