Poorly written protocols can lead to costly protocol amendments, missed milestones, decreased data quality, site disengagement, and poor enrollment rates. Inderoâs clinical scientists collaborate with seasoned medical, regulatory, and operational experts to draft high-quality study protocols that meet timelines and scientific standards.
Draft ProtocolÂ
A clinical scientist with in-depth knowledge of dermatology and rheumatology therapeutic areas drafts the protocol using adapted tools, well-defined templates, and checklists.
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Quality Control & Internal Review
Peers perform quality control on the initial protocol draft.
KOLs and renowned investigators with relevant experience in your dermatology or rheumatology indication review the protocol to ensure itâs scientifically sound and practical.
Review by Innovaderm CRU
Protocols are also reviewed by experienced Clinical Research Coordinators from our own CRU, who understand a siteâs reality, ensuring feasibility at a site level, reducing potential site protocol deviations and amendments.
Final Protocol
After all reviews and revisions are complete, the final protocol is produced.
Celebrating 25 Years of Therapeutic Excellence
For a quarter-century, Indero has been the trusted CRO partner for biotech and pharmaceutical leaders across the globe, delivering precision, reliability, and innovation in dermatology and rheumatology clinical trials.
Structured documents that are continually updated and revised as per the most recent guidelines (ICH, ethics, etc.).
Dual-Focus on Dermatology & Rheumatology
An extensive list of indication-specific clinical assessments and patient-reported outcomes (PROs).
Templates & Checklists
Built upon many years of experience in working with various dermatological and rheumatological indications.
Partner with Indero for Study Design & Protocol Writing
Indero is a dual-focus CRO for dermatology and rheumatology clinical trials that offers a robust and collaborative study design and protocol writing process for successful clinical trials. Tell us about your clinical trial.
Study Design & Protocol Writing Services that Accelerate Studies
Scientific discipline. Operational efficiency. Clinical development expertise. Our study design services provide the rigorous foundation, quality data, and expertise dermatology and rheumatology studies need to ensure effective execution and on-time delivery.
âCongratulations to the team for a very positive pre-IND meeting outcome! Your dedication and well-executed plans have laid a strong foundation for our program. This success is a significant trust-building milestone with the agency. Thank you for your outstanding work!â
Thibaud Portal
Founder and CEO Alys Pharmaceuticals
Andrea Epperly
Global Head of Project Management Alys Pharmaceuticals
Wherever Youâre Going, Weâre all in.
Need help with your next study? We want to learn more. Fill out the form on the right and one of our experts will be in touch.
Inderoâs Early Phase 1 model enables sponsors to initiate topical studies that detect early pharmacodynamic signals much sooner than traditional phase 1, using microdosing and transcriptomic analysis. This approach reduces preclinical requirements, shortens study duration from 8â12 weeks to â€3 days, and lowers costs, helping teams make informed go/no-go decisions faster.
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