PharmTech spoke with Dr. Asma Patel, VP Global Commercial and Scientific Consulting–Drug Product, to find out how the growth ...

HRV Pharma’s innovative “virtual manufacturing” model connects FDA-approved facilities to prevent prescription shortages and ...

Next-generation automation is closing the gap between curative science and real-world demand, enabling faster development, ...

Enveda has been using AI to power its drug discovery platform for several years. The company injected $230 million into ...

The U.S. Food and Drug Administration has awarded the National Institute for Pharmaceutical Technology and Education a grant worth up to $35 million over the next five years to improve drug ...

Zee Laboratories supplies medicines to government hospitals and institutions such as AIIMS, as well as to central and state ...

A CDMO championing a commitment to patients may sound like lip service or branding, but truly patient-centric CDMOs offer ...

Drugmakers told the FDA that inflexible post-approval change requirements are among the top regulatory barriers to the ...

Discover how early CMC, process optimization, and formulation strategy drive scalable, commercially viable drugs.

From the moment we could look up to the skies, humanity has dreamt of what’s up there. And once we got there, how could we master it? And now that we’re there all the time, how can we use it? In 2025, ...

Developing high-quality, safe, and effective drugs is a complex process that requires varied scientific skills and stringent regulatory assessments. Drug development is a process that spans many years ...