April 24, 2025
Nasal spray repositioning through the 505(b)(2) regulatory pathway has emerged as a compelling approach, offering a unique opportunity to breathe new life into existing drugs and improve patient experiences.
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December 9, 2024
Throughout your nasal spray development journey, you are likely to face pressure to accelerate timelines to clinical phases, stemming from the need to:
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April 24, 2024
Rohit Mulik, Senior Manager: Formulation R&D, and Eric Kaneps, VP, Sales & Marketing at Renaissance Lakewood LLC, answer questions about the challenges in nasal drug delivery and outline how CDMO partnerships can help to overcome them.
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Supporting nasal product R&D and clinical manufacturing at Renaissance Learn more about the Nasal Product space and how Renaissance is making an impact.
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October 19, 2022
Overview: The following case study is a collaboration with Renaissance Lakewood and Raven consulting on continuous...
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October 6, 2022
A look at the interconnected role of the formulation, formulation excipients, and nasal spray...
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September 20, 2022
A review of nasal spray formulation excipients and their potential for enhancing drug delivery. Test
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August 22, 2022
When developing a sterile product, people often do not understand what’s required to manufacture the product....
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August 1, 2022
A CDMO is a Contract Development and Manufacturing Organization that accelerates how pharmaceutical companies bring drugs and therapies to market. The drug discovery to market pipeline is filled with many challenges, partnering with a CDMO lowers the risk and capital investment associated with this multi-step, multi-year, and often multi-million-dollar process.
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June 11, 2021
Nasal spray devices are used to deliver both locally and systemically acting pharmaceutical products,1 and are readily available in the marketplace in unit dose and metered multi-dose formats.
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