Clinical

Study Design and Protocol Writing

In-depth expertise in creating successful trials

The integrity and consistency of the study protocol, including the chosen endpoints, are key to a clinical trial’s success. At Alira Health, we understand the importance of focused study design and are experts in producing comprehensive, well-written protocols.

With a focus on accuracy and consistency, our team works to ensure the study protocol makes sense both scientifically and logistically—a benefit to all partners and participants.

Support and guidance tailored to your needs

From the outset, our team works to understand all the complexities of the project, including indication-specific measures—an aspect that sets Alira Health apart among contract research organizations (CROs).

You can expect frequent communication and collaboration with our study design team as they tailor guidance to your specific business needs and trial requirements. Our study design and medical writing services include:
  • Protocols
  • Informed consent forms
  • Clinical study reports
  • FDA briefing documents
  • Investigator’s brochures
  • Abstracts, posters, and journal articles
  • Executive summaries for efficacy or safety
  • Patient narratives

Why choose Alira Health?

With Alira Health industry leading CRO as your partner, you will benefit from:

  • Exceptional customer service and site relations
  • In-depth expertise across the entire clinical trial process
  • Flexible and tailored service delivered by multidisciplinary and global teams
  • Frequent, transparent, and professional communication
  • Guarantee we will lead your study efficiently, safely, and successfully

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.