Biometrics

Medical Writing

Clinical reporting expertise

Convert the complexity of your clinical trial information into clear, understandable documentation. Our medical writing services provide full support for Phase I–IV clinical trials and medical device study documentation.

In-depth industry expertise

 

Our global team of medical writers produces technical and scientific documentation for a wide range of studies for both the EMA and FDA. Our writers have experience in over 40 therapeutic areas and hundreds of indications, and are native or fluent English speakers, with additional bilingual writing capabilities.

Comprehensive support for all your documents:

  • Protocols
  • EMA and FDA Briefing Packages
  • Investigator Brochures
  • Clinical Study Reports (CSR)
  • Marketing Documentation
  • Posters and/or Abstracts
  • Customized reports based on client requests
  • Development of scientific publications

Why choose Alira Health?

Together, the CROS NT and Alira Health biometrics team has provided expert statistical guidance for over 500 projects. As our partner, you’ll benefit from:

  • In-depth expertise across the complete clinical trial process
  • Flexible, tailored service delivered by global multidisciplinary teams
  • Efficient, safe, and successful study leadership
  • Exceptional customer service and site relations
  • Frequent, transparent, and professional communication
  • Comprehensive statistical guidance for regulatory communication and submission, study-based data management, biostatistics, and statistical programming

Related News

Multimedia May 19, 2022
Fireside Chat Replay: Latest Developments in Oncology Supportive Care
In this fireside chat, we sit down with two medical experts in oncology and discuss some of the fascinating developments that are happening in the oncology supportive care field.
Clinical
Events May 19, 2022
DIA 2022 Global Annual Meeting
We are pleased to announce that we will be joining DIA 2022 Global Annual Meeting as exhibitors and delegates.
Biometrics Clinical Life Sciences Regulatory
Events May 9, 2022
7e Journée start-up innovantes du dispositif médical
Clinical Digital Health Market Access MedTech Research & Development
Multimedia April 28, 2022
Alira Health’s Transformation Talks: Real-World Data to Support HTAs in Europe
Learn more about RWD as a support in HTAs and its direct impact on HTAs budgets, results, and even patient outcomes by listening to this episode of Transformation Talks.
Clinical Market Access RWE
Multimedia April 15, 2022
Alira Health’s Transformation Talks: Real-World Evidence Strategy Playbook
As a special guest, our episode “Real-World Evidence Strategy Playbook” with Romain Finas, Vice President of Real-World Evidence at Alira Health, is now live! Listen to this podcast(...)
Clinical RWE
Multimedia April 13, 2022
Fireside Chat Replay: Clinical Trials in Rare Disease: Best Practices for Integrating the Patient Voice
This webinar will focus on the U.S. FDA and EU MDR/IVDR regulatory pathways and strategies for medical device startups based in the Asia Pacific.
Clinical Patient Engagement
Events April 12, 2022
SCOPE Europe 2022
We are thrilled to announce that this year we will be joining the 4th Annual Summit for Clinical Trials Operations Executives Europe (SCOPE Europe).
Clinical
Welcome to Alira Health. This site is best viewed in Chrome, Microsoft Edge, or Firefox.