litt-adkison.com
Memberships -
http://www.litt-adkison.com/Memberships,__p3.php4
DGRA - German society of Regulatory Affairs. The Institute of Clinical Research.
3rpc.net
Expertise - 3R Pharma Consulting - reducing regulatory risk
http://www.3rpc.net/index.php/expertise.html
Dr Manuel Zahn, founder and managing director of 3R PHARMA CONSULTING, offers expertise in the area of GMP, Regulatory CMC / Quality and stability testing of pharmaceutical products. 29 years experience in the pharmaceutical industry (in Germany and Sweden). 25 years experience in Regulatory Affairs (world-wide). Qualified Person (QP) according to Directive 2001/83/EC, Art. 49 and 51. APIC Certified Auditor of API manufacturers (ICH Q7). Negotiation skills in a cross-cultural environment.
3rpc.com
Expertise - 3R Pharma Consulting - reducing regulatory risk
http://www.3rpc.com/index.php/expertise.html
Dr Manuel Zahn, founder and managing director of 3R PHARMA CONSULTING, offers expertise in the area of GMP, Regulatory CMC / Quality and stability testing of pharmaceutical products. 29 years experience in the pharmaceutical industry (in Germany and Sweden). 25 years experience in Regulatory Affairs (world-wide). Qualified Person (QP) according to Directive 2001/83/EC, Art. 49 and 51. APIC Certified Auditor of API manufacturers (ICH Q7). Negotiation skills in a cross-cultural environment.
dra.uni-bonn.de
Courses — Fachgruppe Pharmazie
https://www.dra.uni-bonn.de/courses
Commencement of the postgraduate study course. Commencement of the postgraduate study course. Master course: Master of Regulatory Affairs in co-operation with the German Society for Regulatory Affairs (. The School of Pharmacy hosts a colloquium every Monday during lecture period in hall 1, Gerhard-Domagk-Str. 3. We are glad to welcome guests! Can be found here. Furthermore, a Drug Research M. Sc. module Drug Regulatory Affairs is offered to postgraduate students. Uni Bonn Created by: drug. Dec 18, 2009.
vivoscience.de
Downloads | vivo Science GmbH
http://www.vivoscience.de/downloads
More than just immunology. News / Messen / Veranstaltungen. 49 (0) 2562 - 81 70 0. Auf dieser Seite können Sie wissenschaftliche Artikel (Dossiers), Präsentationen, Veröffentlichungen und Informationsmaterial laden:. Prüfung der Allergenität und Anaphylaxie (engl.). Prüfung der Immuntoxizität (engl.). Präklinische Prüfung neuer Arzneimittel (engl.). GLP Training / Schulung für Prüfpersonal (deutsch). GMP Training / Schulung für Prüfpersonal (deutsch). Allgemeine Firmen-Präsentation (engl.). Unverbindlich...
gloorlang.com
Medizintechnik Jobs in Deutschland, Österreich und Schweiz
http://www.gloorlang.com/medizintechnik-jobs-deutschland-oesterreich-schweiz-17
Medizintechnik Jobs in Deutschland, Österreich und Schweiz. 41 (0) 61 206 6181. Mit unseren Partnern sind wir stark! Website by delineo communication.
e-dra.com
Speaking - e-DRA Harmsen
http://e-dra.com/4.html
Consultancy for Electronic Document Management and Regulatory Affairs Systems. Contact l Legal Notice. Experience Exchange: Document management and regulatory publishing tools and systems. 26th February 2014, London, Global eCTD Management. More info at: www.informa-ls.com/eCTD. Dokumentenmanagement für Regulatory Affairs. 6 - 9 März 2014 , Universität Bonn - Master of Drug Regulatory Affairs. Weitere Informationen unter: http:/ www.dgra.de. Regulatory Information Management, SME Breakfast Briefing.
e-dra.com
EDMS - e-DRA Harmsen
http://e-dra.com/2.html
Consultancy for Electronic Document Management and Regulatory Affairs Systems. Regulatory Information Management (RIM). Other R&D IT systems. Contact l Legal Notice. ESubmission Ready Document Management. Electronic Trial Master File. Capa and Deviation Management. Records Management / Archiving. CMC Batch Records Archive. Write User Requirements, select and implement an EDMS and Deviation / CAPA system (Biotech Company). Write User Requirements and select cloud EDMS vendor (Biotech Company). 28th - 30th...
scire.ch
scire • Links
http://www.scire.ch/links.php
European Federation of Biotechnology.