RNA Clinical Trials Solutions

1. Regulatory Strategy And Submission Support 8/13/2025

   Eliminate delays and ensure seamless regulatory alignment with an experienced toxicology services team.

2. 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.

3. The Future Of Reimbursement For Cell & Gene Therapies 7/27/2022

   Our team excels at understanding the ever-changing and complex healthcare market and helping clients solve issues. Learn about the payer challenges, potential reimbursements, and the competition to consider.  

4. Clinical And Regulatory Strategy 11/7/2023

   Many biotechnology companies come to Australia to conduct early phase clinical trials and take advantage of straightforward regulatory streams and of the lucrative 43.5% R&D cash refund scheme. Biotechnology companies then often look at locations in Asia, such as South Korea, Thailand and China to tap into their huge treatment-naïve patient populations for their later phase clinical research.

5. Recruit Patients Faster In The Asia-Pacific Region 9/29/2022

   Novotech relies on years of experience, in-country knowledge and real-life big data to identify and propose the best-performing sites and investigators for your study.

6. Trusted Partner For Clinical And Regulatory Success 7/15/2025

   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.

7. Oncology CRO Services 11/7/2023

   Biotechnology companies are facing increased challenges around participant recruitment and retention, lengthy timeframes and relatively high costs.

8. Real World Data 6/27/2023

   Accelerate patient recruitment and drug development with real world data (RWD).

9. Your Vision. Our Pioneering Experience. 3/10/2021

   PRECISION ADVANCE, a collection of interconnected services and complementary teams, uniquely focuses on the complexities of clinical, regulatory, manufacturing, and commercial needs to successfully bring cell or gene therapies to market.

10. Accelerate Your Drug Development With A Global Partner 8/13/2025

    With the right Chemistry, Manufacturing & Controls (CMC) consulting services, your organization can excel in early-stage strategizing, accelerate timelines, optimize processes, and reduce costs.