Press release
Quality Documentation of Medicinal Substances incorporated in Medical Devices
In order to demonstrate appropriate quality for incorporated medicinal substances in medical devices (ancillary medicinal substances), applicants need to provide information and scientific data, which are similar to that requested by authorithies for API"s in medicinal products. These data are submitted to the competent authorities by the notified body involved. FORUM Institut für Management extend to this tender subject an intensive seminar. The attendant limiting allows great deal of discussions.FORUM Institute fuer Management, one of the leading professional seminar and conference providers in Europe, offers a seminar for the pharmaceutical and medical device industry in english language on 7 July 2009 in Frankfurt/ Airport.
Further information on the seminar and the company you will find under:
http://www.forum-institut.de/de/veranstaltungen/pharma-kosmetik-medizin/veranstaltung/details/0907283-quality-documentation-of-medicinal-substances-incorporated-in-medical-devices/
FORUM Institute is very active and acknowledged in the field of educational seminars and conferences for the pharmaceutical industry. In several areas FORUM has the leading market position. Especially the close co-operation with the regulatory authorities assures the outstanding quality and up-to-dateness of the trainings. Each novel important guideline from the national authorities or the EMEA/CHMP results in a seminar within a short period of time to insure that pharmaceutical industry personnel receives the proper information and training. The speakers are experts from the pharmaceutical industry, service provider, lawyers and national / international authorities.
Contact
Christiane Freitag
Eventmanager pharma & medical device
FORUM Institut fuer Management GmbH, Heidelberg
Vangerowstraße 18
69115 Heidelberg
Tel. 0049 6221 500 680
Fax. 0049 6221 500 618
c.freitag@forum-institut.de
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