PharmTech.com serves as a leading information hub for professionals involved in pharmaceutical manufacturing and drug development worldwide. Drawing on the expertise of Pharmaceutical Technology and Pharmaceutical Technology Europe, it delivers comprehensive coverage of topics spanning medicine and healthcare, pharmaceuticals, diagnostics, alternative medicine, natural sciences, as well as emerging fields like artificial intelligence and machine learning within the industry.
The platform’s readership primarily consists of scientists, researchers, regulatory professionals, executives in pharma companies, and other stakeholders who require up-to-date insights into industry trends and technological advancements. PharmTech.com is particularly valuable to those seeking expert commentary on evolving scientific practices or looking for detailed event coverage relevant to pharmaceutical innovation.
PharmTech.com covers its subject matter through a mix of press releases from private sector organizations, expert analysis pieces that interpret new research or regulations, and reports from key industry events. This approach ensures that readers receive both timely news updates and deeper contextual understanding necessary for informed decision-making.
Content is distributed across multiple platforms including print editions for traditional readers as well as robust online digital formats to reach a global audience efficiently.
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The aim of this study was to develop and optimize an orally dissolving film formulation containing a blend of active ingredients in a strategic combination of natural and synthetic excipients to achieve a balance between controlled actives release and rapid onset of action.
MilliporeSigma's Sebastián Arana explains why modular, digital, platform-based manufacturing, not raw capacity, will define biomanufacturing's next decade.
Kristin Ciriello Pothier, KPMG US, discusses deal discipline, manufacturing diligence, and why oncology and GLP-1s are driving biopharma M&A activity in 2026.
At BIO 2026, Thermo Fisher's Anil Kane explains how AI is reshaping CDMO workflows and what biotechs should prioritize when choosing a development partner.
MilliporeSigma's Sebastián Arana breaks down CGT manufacturing's biggest scale-up gaps and why supply chain collaboration is now essential.
The agency approved palbociclib with trastuzumab, with or without pertuzumab, and endocrine therapy for the maintenance treatment of HR-positive, HER2-positive metastatic breast cancer.
This episode of Pharma Fundamentals explains the difference between a quality system for biologics compared with small-molecule drugs and the Parenteral Drug Association's revision to Technical Report No. 56.
The future of synthetic biology will depend not only on the ability to design biological systems, but on the capacity to manufacture DNA reliably at scale within regulated frameworks.
How the Lehigh Valley Economic Development Corporation is building a technical workforce pipeline to support Eli Lilly's 850-job pharmaceutical manufacturing expansion.
What pharma's regulatory writers can borrow from clinical AI before the next inspection.
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