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Blog
Rigorous Sample Handling Processes
Ensuring that current and relevant FDA and EMA guidances are applied to the handling of bioanalytical samples during clinical trial conduct is crucial. This month's blog, including podcast, offers an expert look at the considerations.
Blog
From Lead Candidate to In-life Use
The development of pharmaceutical products, in dosage forms that the human body can safely and effectively metabolize, is a challenging undertaking. In this month's blog, we offer insight on the process, and a related podcast featuring our CDMO experts.
Blog
Participant Retention Strategies in Phase I Clinical Trials
Learn some of the key strategies Altasciences employs to ensure you have the participants you need for your studies.
Blog
Get Up Close and Personal with Dr. Anahita Keyhani, PhD
Get to know Dr. Anahita Keyhani, PhD, Senior Director of Scientific Operations, Mass Spectrometry and Method Development, at Altasciences.
Blog
Clinical and Regulatory Considerations for Developing COVID-19 Treatments – a Discussion with our Experts
As the COVID-19 pandemic evolves across the globe, the search for effective therapies also continues to gain momentum, including the possibility of repurposing existing medications that may show effectiveness against COVID-19 symptoms.
Blog
Microsampling - Making a Difference in Drug Development
Blood microsampling is a less invasive and simplified alternative to traditional venipuncture, and provides significant advantages in preclinical and clinical studies alike. This month's blog includes an overview, and additional information.
Blog
Vaccine Development Blog/Podcast
Vaccine development is a complex, time-consuming process at the best of times. Now, facing a world-wide pandemic of a novel virus, understanding the science, the regulatory process, and the desire for an immunization solution has never been more crucial.