Partnering Solutions
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Clinical Trial Regulations
4/11/2025
This essential guide walks through mastering the complex landscape of clinical trial regulations, providing a clear, practical breakdown of regulatory timelines, legal obligations, and more.
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Bioanalysis Solutions
8/24/2024
Learn how a bioanalytical testing partner with comprehensive solutions and unwavering commitment to quality can help you bring safe and effective drugs to market with confidence.
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The inSeption Group Difference
5/31/2023
Discover how inSeption Group distinguishes the right people as the most impactful variable of any outsourcing equation and contributes to the delivery of life-changing therapies.
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Toxicology Support: Regulatory Strategy And Submission Support
12/2/2025
Eliminate delays and ensure seamless regulatory alignment with an experienced toxicology services team.
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Simplifying The Patient Journey With One App
11/12/2025
A single mobile app simplifies clinical trial participation by unifying eConsent, IRT, and eCOA workflows, reducing patient burden and improving engagement across trial phases and locations.
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DSG Clinical Trials Products And Software Solutions
12/5/2011
Since our founding, DSG has transformed clinical trial data collection and analysis with its integrated suite of EDC software solutions. Below is a wide range of clinical trials software and services that we offer to our clients.
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Drug Development Experience For Biotechs
8/8/2024
Leverage our extensive expertise across over 120 therapeutic indications to drive your success.
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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.
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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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Dual Sourcing: Mitigating Risk In Your Supply Chain
8/22/2022
Dual sourcing should be implemented to reduce risk and ensure an uninterrupted supply of critical, life-saving therapies. Recent FDA draft guidelines recommend risk management plans to prevent drug product shortages.