Pharma Unternehmensberatung Dr. Aye und Partner Lüneburg  
zur Startseite

Rolf-Dieter Aye

German, born in 1940
Pharma-Unternehmensberatung Dr. R.-D. Aye
Reiherstieg 22
D-21337 Lüneburg | Germany

Tel.: ++49-4131-36725
Fax: ++49-4131-603250
EDUCATION Profession: Pharmacist
Doctor of science (Dr. rer. nat.) in pharmaceutical chemistry from the university Tübingen, Germany 1967
PROFESSIONAL CURRICULUM 1968 until 1972 Merck, Darmstadt, leader of a laboratory of the pharmaceutical development plant, especially occupied with the method techniques of the production of solid drugs

1972 to 1974 Dr. Thilo in Dortmund, head of quality control in pharmaceutical development, especially working in the fields of eye drugs and injection fluids

since 1974 head of Dr. Aye & Partner, consultant in all technical pharmaceutical affairs

in between 1983 and 1993 general manager of technical affairs of Lichtwer Pharma GmbH in Lüneburg and Berlin, responsible for development, production and quality control of drugs, regulatory and patent affairs

expert for pharmaceutical chemistry and drug registrations

since 1997 official external expert of the German Authority for Regulatory Affairs (BfArM) for the quality of herbal drugs and biopharmaceutical aspects
FIELD OF ACTIVITY Rolf-Dieter Aye is acting as an attested expert by the certification of pharmaceutical documentations for drug registrations and of pharmaceutical production plants in regard to the EU-Legislation and to GMP conformity.

Rolf-Dieter Aye advises besides his work as an expert several pharmaceutical companies concerning questions of pharmaceutical production and quality control and regulatory affairs. As a further activity Rolf-Dieter Aye is acting as a consulter in the conformity assessment procedure for medical devices.

He is member of the following scientific associations: Society for Medicinal Plant and Natural Product Research Deutsche Pharmazeutische Gesellschaft e.V.

He participated decisively in the planning and realisation of several new pharmaceutical plants, concerning mainly the production of solid drugs on a high technical level, corresponding to the GMP-rules, including the implementation of quality assurance systems.
Datenschutz Impressum Startseite Aktivitäten