06.26.24 -- So You Want To Be An Outsourcing-Industry Entrepreneur?

As the use of AI increases and expands to new functional areas within biopharmaceutical companies, leaders must understand the risks and mitigate the impact of hallucinations in AI model outputs.

Disinfectant efficacy studies are crucial for safeguarding the sterility of your manufacturing facilities. Review intricacies and how to design this important study.

It is important to develop robust, reliable processes to safeguard APIs. Explore best practices to provide patients with high-quality treatments that meet their therapeutic requirements.

Ensure your press is running with optimal efficiency by expanding your knowledge of proper cleaning and maintenance.

Process parameter and quality attribute relationships, including those for typical pre and post spray-drying unit operations, will be explored in the context of real-world examples.

PBPK modeling advancements are helping drug sponsors mitigate risk in preclinical and clinical studies through early identification of poor absorption properties.

Examine the case study and learn how formulating an orally disintegrating tablet (ODT) created a convenient dosage form with a shorter T_max for the treatment of acute migraine.

Our team of experts can assess processes for suitable application of continuous flow culminating in the custom development of processes incorporating proof-of-concept to cGMP manufacturing and commercialization.

Explore this interactive PDF with information about technologies & end-to-end integrated CDMO services provided by Adare Pharma Solutions.

A CDMO with the right team of experts can aid development, regulatory compliance, and clinical trial supply, accelerating timelines to first human dose trials and the path to market.

We are capable of supporting a wide range of ophthalmic services and deliver excellence in individual solutions with customers in mind.