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 OmniScience SA |
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OmniScience SA
32, rue du Prieuré
CH 1202, Geneva
Switzerland
Email: gerard.mcgregor@omniscience-ltd.com
Web: www.omniscience-ltd.com
Title: PhD
First Name: Gerard
Last Name: McGregor
Phone: +41(0) 22 751 1850
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
o anti-angiogenic drugs, oncogene drug targets
• neurology
o pain neuropharmacology, antidepressants
• gastroenterology
o brain-gut axis, mucosal immunology, GI peptide hormones
• endocrinology & diabetes
o peptide hormone pharmacology & metabolism, GPCRs, incretins
• nutrition
o novel food supplements, scientific & regulatory aspects
• critical care medicine
o antioxidant drugs in critical care medicine
• herbal drugs & natural products
o pharmacological & toxicological screening
• identifying experts & key-opinion-leaders
o initiating & nurturing contact
• reporting on medical scientific congresses
o congress attendance & preparing written reports of proceedings
• pre-clinical toxicology
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