spacer.png, 0 kB

Newsflash

Registration is now open for the 2nd EMWA/ICR joint symposium in London on 24th February 2008. Places limited so don’t delay.
 

JOBS

Vacancies for medical writers and editors 

FREELANCER LIST

List of registered freelance medical writers and editors 

EMWA-ICR Joint Symposium

Details of the EMWA-ICR Joint Symposium in London.

COMPANY LIST

List of registered medical writing and other companies 

Search
Dr. med. Ruth Behrens

Dr. med. Ruth Behrens

Dr. med. Ruth Behrens

medexx the medical expert writers
Enkendorf 8
D-24631 Langwedel Germany
Email: medexx@hamburg.de
Web: www.medexx.eu
Title: Dr. med.
First Name: Ruth
Last Name: Behrens
Phone: +49(0) 4329 913 109
Fax: +49(0) 40 181 588 56
Mobile: +49(0) 151 520 540 25

Skills And Services Offered:
Due to my 25 years of pharma business experience
I am glad to offer a wide variety of services:
Medical and Scientific Education
Training Documents
• Pharmaceuticals Sales Representatives
• Medical device Sales Representatives
• Modules for E-Learning
Patient Information
• Health information systems
• Information brochures
• Digital patient information systems
Scientific Promotion
• Peer reviewed articles
• Abstracts
• Posters
• Medical book chapters
• Literature reviews
• Proof reading
• Presentations
• Brochures
• Monographs
• Newsletters
Medical Journalism
• Journal articles
• Newsletters
• Congress reporting
• Medical and scientific literature reviews
• Cochrane research
• Evidence Based Medicine research

Translation Services
English German / German English
• Manuscripts
• Medical charts and patient records
• Doctoral theses
• Clinical and preclinical expert reports
• Dossiers
• Data sheets
• Manuals
Specialization in the translation of documents for
• Pharmaceuticals
• Medical devices
• biotechnology
• healthcare
• medical research


Expertise:
Regulatory Writing
• Clinical and Preclinical Overviews
• Clinical Summaries
• SmPC, PIL and Labelling
• CTD - Module 3 and 4
• Deficiency Letter Correspondence
• Standard Operation Procedures SOP s
Pharmacovigilance activities
• Evaluation of safety data
• Serious Adverse Event narrative writing
• Management of Serious Adverse Event data
• SUSAR reporting to Ethics Committees and national Regulatory Authorities
• Individual case reports to the Eudra Vigilance Post-Authorisation Module
• Periodic Safety Update Reports (PSUR)
• Safety reports - quarterly and annual
• Investigator brochures safety information and updating
• Risk management plans
• Risk benefit assessments
Clinical trial documents
• Study protocols Phase II-IV
• Case Report Forms
• Investigator brochures and annual updates
• Informed Consents
• Ethic Commission applications
• Study Reports
• Post Marketing Surveillance trial documentation


Other Information:
I am offering a Last ! Minute Service
In case Murphys Law has hit you ...
I am lending you a strong hand
by making the impossible possible.
In case you are pressed for time
and your staff can't hold an important deadline
Please note our 24 hours hotline
+49 151 520 540 25
medexx@hamburg.de_____


Date added: 2008-7-16 14:44:43    Hits: 418
Powered by Sigsiu.NET RSS Feeds
spacer.png, 0 kB