About Us
Our Writers
We are a virtual consultancy, with a global team. Our team averages over 15 years of experience in the Pharmaceutical industry and are qualified to BSc, MSc/M Pharm or PhD level.
From start to finish, your project will be handled by one of our writers. All our writers possess the skills required to maintain effective and professional communication in order to deliver a project that meets your unique requirements.
Our proven and successful model has meant that approximately 80% of our business is repeat business. We have also developed strong relationships within the industry.
Our Biostatisticians
Biostats and Medical Writing go hand in hand, and as such, Armah Consultants works closely with a crop of talented Biostatisticians, who have the expertise to lead discussions in the development of clinical protocols (including but not limited to discussions on endpoint selection, sample size, methodology, analysis, and study design development) and propose analytical strategies.
Our Biostatisticians have experience managing all statistical aspects of clinical studies using SAS and R Programming, CDISC, and numerous other statistical computation programs.
Your Project
Our global presence allows us to take advantage of the differing time zones of our writers, thus extending the amount of time our team can spend on a document within a 24-hour window. A valuable asset when required to meet aggressive timelines in a face-paced and evolving industry.
Our team of writers are well-versed in the strategic planning and authoring of documents for the following submissions in the US, UK, EU, Japan and BRIC countries.:
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New Drug Application (NDA)
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Marketing Authorisation Application (MAA)
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Investigational New Drug (IND)
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Biologics License Application (BLA)
Where applicable, all documentation can be provided publish-ready or submission-ready at the request of the client and can be adapted to any client specification (client style guides and SOPs).
We ensure that all documentation are ICH-GCP complaint, and meet the needs of regulatory requirements.
Prior to completion, all documentation undergo a thorough proof-reading and Quality Control (QC) validation process.
For more information on the services we provide click here or contact us.