RNA Clinical Trials Solutions
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Cell & Gene Therapy Clinical Development Testing
4/23/2026
By combining scientific depth with operational scale, we help sponsors make confident, data-driven decisions, reduce development risk, and accelerate the path from discovery to clinical impact.
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New Next-Generation GMP Facility
5/16/2023
A new state-of-the-art GMP facility has been created to accelerate the development of CRISPR-based cell and gene therapies, overcoming challenges such as procuring reliable GMP-grade sgRNA persist.
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Earn The Trust Of Biotechs And Emerging Pharma
12/10/2025
Backed by a global team of more than 3,000 professionals across 34 office locations, we deliver scalable, high-quality clinical development solutions tailored to the needs of emerging and mid-sized biotech companies.
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Site Management Organization
11/7/2023
Discover the power of clinical excellence with Acrostar's SMO Division, a dedicated entity operating as part of Novotech.
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The Importance Of Patient Recruitment In Clinical Trials
3/28/2025
Why Patient Recruitment Matters in Clinical Research
Patient recruitment is one of the most critical aspects of a clinical trial’s success. Without an adequate and diverse participant pool, trials risk failing to generate reliable and representative data. Ensuring sufficient participation is essential for producing statistically valid results that confirm the treatment's safety and effectiveness.
For biotech companies, especially those under tight timelines and budgets, partnering with an experienced CRO like Novotech ensures that patient recruitment efforts are both efficient and effective, enabling timely trial completion and robust data collection.
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Patient Recruitment And Site Selection
12/20/2022
Novotech relies on years of experience, in-country knowledge, and real-life big data to identify and propose the best-performing sites. Uncover the possibilities for your next study.
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CMC: Accelerate Your Drug Development With A Global Partner
12/2/2025
With the right Chemistry, Manufacturing & Controls (CMC) consulting services, your organization can excel in early-stage strategizing, accelerate timelines, optimize processes, and reduce costs.
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Trusted Partner For Clinical And Regulatory Success
12/2/2025
Novotech’s Regulatory Affairs team offers customized, end-to-end clinical and regulatory solutions, guiding biotechnology, pharmaceutical, and medical device companies through the entire product lifecycle.
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Orphan And Rare Disease CRO Services
11/7/2023
Rare disease clinical studies demand a specialized full-service CRO with expertise in enrollment, site selection, and global regulatory knowledge for accelerated recruitment.
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Pharmacometric Services
6/27/2023
Our talented and experienced team can assist in all Clinical Study Phases (Phase 0, I, II and III) and in study designs ranging from First in Human (FIH), Single Ascending Dose (SAD), Multiple Ascending Dose (MAD), Drug-Drug Interaction (DDI), Bioavailability/Bioequivalence (BA/BE), Food Effect as well as Special Population studies.