Company Listing

The company listing is a subscription service that allows EMWA members and non-members the opportunity to advertise their company's products and/or services. The companies listed below are companies that may be of interest to medical writers and editors and who have chosen to have their services displayed. It is not EMWA policy to vet these entries and entry in this list does not imply any form of endorsement by the European Medical Writers Association. These entries and list cannot be reproduced elsewhere without express permission.

Please note that EMWA will refer any requests for training or related enquiries to the company listings which is an additional benefit of advertising your details with EMWA.

Membership of the company listing is on an annual basis (from Jan through to Jan), and subscription fees are given below:

The total annual listing fee for EMWA members is €500

Join in October - pay for 15 months i.e. €626
Join in November - pay for 14 months i.e. €584
Join in December - pay for 13 months i.e. €542
Join January to September - pay €500

The total annual listing fee for non-EMWA members is €1000

Join in October - pay for 15 months i.e. €1249
Join in November - pay for 14 months i.e. €1166
Join in December - pay for 13 months i.e. €1083
Join January to September - pay €1000

To apply to add your company to our listing, please click here to download the application form, and then email your completed application form to webadmin@emwa.org

 

OmniScience SA




5 Rue Liotard
CH-1202 Geneva
Switzerland
Email: ron.hogg@omniscience-ltd.co
Web: www.omniscience-ltd.com
First name: Ron
Last name: Hogg
Phone: +41(0) 22 751 1850
Fax:
Mobile: + 41 79 773 2495

Skills And Services Offered:

OmniScience SA are based in Geneva, Switzerland. We are 3 Professional Scientific & Medical Writers and are all native English-speakers and Multilingual (German, French, Italian, Spanish).

We are PhDs with substantial publication records.

We are fully-acquainted with drug regulatory & clinical research guidelines (ICH, EMEA, FDA) and with publications guidelines (CONSORT, STROBE, GPP).

We specialize in compiling Regulatory Documents for the Pharmaceutical Industry and provide the full range of Pre-Clinical and Clinical Regulatory documents. We have particular experience in:

  • Writing & compiling non-clinical & clinical CTD modules
  • Providing quality-assured eCTD-compliant non-clinical and clinical modules
  • Investigator Brochures
  • Clinical Study Protocols
  • Clinical Study Reports
  • Briefing Books & Replies to Authorities
  • Toxicology reports

Our Regulatory Medical Writing experience includes a variety of types of regulatory submissions ranging from INDs to products with well-established use.

For us, writing Original Articles & Reviews for Peer-reviewed Journals is second-nature. We can also prepare:

  • Systematic Reviews and Scientific Assessments,
  • Congress abstracts
  • Medical scientific Projection and Poster Presentations
  • Literature and data-base researches
  • Quality control, quality assurance and translation of scientific manuscripts

Our Academic and Industrial experience spans a broad range of medical scientific areas & activities:

  • oncology
  • anti-angiogenic drugs, oncogene drug targets
  • neurology
  • pain neuropharmacology, antidepressants
  • gastroenterology
  • brain-gut axis, mucosal immunology, GI peptide hormones
  • endocrinology & diabetes
  • peptide hormone pharmacology & metabolism, GPCRs, incretins
  • nutrition
  • novel food supplements, scientific & regulatory aspects
  • critical care medicine
  • antioxidant drugs in critical care medicine
  • herbal drugs & natural products
  • pharmacological & toxicological screening
  • identifying experts & key-opinion-leaders
  • initiating & nurturing contact
  • reporting on medical scientific congresses
  • congress attendance & preparing written reports of proceedings
  • pre-clinical toxicology


Expertise:


Other information: