|
Newsflash
|
Registration is now open for the 2nd EMWA/ICR joint symposium in London on 24th February 2008. Places limited so don’t delay.
|
Dr Alain Y. Platel |
 |
|
APMW
Les Garants
69820 FLEURIE
France
Email: alain.platel@apmw.fr
Web: www.apmw.fr
Title: Dr
First Name: Alain Y.
Last Name: Platel
Phone: +33(0) 474 04 10 37
Fax: +33(0) 474 04 10 37
Mobile:
Skills And Services Offered:
As a 25-year experienced Senior Medical Writer, I provide first-quality medical and scientific writing of virtually any preclinical, clinical and regulatory document for pharmaceutical companies, CROs and academic research institutes. When outsourcing writing of your documents to APMW, you will obtain, within your pre-defined timelines, documents of the best quality available. The following list the main types of documents written, with numbers in brackets:
- Protocols (147),
- Clinical study reports (356),
- Nonclinical reports (31)
- IMPD (85),
- Investigator's brochures (92),
- CTD/eCTD Module 2 (78), Module 4 (18), Module 5 (23),
- Periodic Safety Upodate Reports (32),
- Manuscripts (77),
- Slide and Oral Presentations (43),
- Drug master files (12),
- Translations (118),
- Advice and audit for medical writing activities (11).
Expertise:
Extensive experience in all major therapeutic areas, including:- Anesthesia & resuscitation,
- Biotechnologies,
- Blood and blood-derived products,
- Cardiology & vascular diseases,
- Dermatology,
- Diabetes, nutrition & metabolism,
- Endocrinology & hormones,
- ENT,
- Gastroenterology & liver diseases,
- Gynecology & obstetrics,
- Herbal products and natural extracts,
- Homoeopathy,
- Immunology & allergy,
- Infectious diseases,
- Medical & surgical devices,
- Neurology & psychiatry,
- Oncology,
- Ophthalmology,
- Neurology & respiratory diseases,
- Rheumatology,
- Vaccines.
Documents written are of the best quality available and are submitted to a double quality-control check before release.
Translations to- and from English and French of any clinical document or presentation.
Other Information:
Advice and audit for Medical Writing in pharma and biotechnology companies and in CROs, in order to achieve an improvement of the quality and timelines of internally written clinical and preclinical documents.
|
|
|
|
|
|
