All
Amarex medical writing projects are conducted in close synergy with
our clients as well as the Amarex biometrics, regulatory affairs,
and quality assurance departments.
Amarex medical writers are experienced scientists
with advanced degrees in the biological sciences and related fields,
affording them the experience to compile study-related data into
comprehensive and understandable reports and submissions that are
ICH/FDA compliant. A hallmark of all Amarex study reports and manuscripts
is the use of reader-friendly graphics, supported by statistical
tables and listings of trial data. A major timesaving advantage
to Amarex clinical study reports is the preparation and client approval
of a front-loaded shell early in the conduct of the trial.
Our medical writing professionals are experienced
in word processing, graphics implementation, and document production.
Medical writing experience includes all major therapeutic areas
as well as pharmacology, immunology, infectious diseases, document
assembly, filing and or publication of research oriented documents.
Amarex Medical Writing Services:
- Integrated Clinical and Statistical Study Reports,
Including Pharmacokinetics
- Statistical Reports
- Investigator Brochures
- Protocols
- Manuscripts and Abstracts
- U.S. and International Regulatory Submissions
- Safety and Efficacy Summaries
- NDA, ISS, ISE
- INAD, NADA
- BLE
- IDE, PMA
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Advantages of AMAREX Medical Writing:
ICH-compliant report template
Front-loaded shell prepared and approved early
Preliminary drafts prepared during active trial conduct
Rapid report / manuscript generation
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