Pharma Lessons has added two new bonus modules to the popular Good Manufacturing Practice Training. The new modules are already available to all currently enrolled users.The first module covers the ...

Discover how outsourcing regulatory submission content development improves efficiency and ensures compliance.

In the evolving landscape of pharmaceutical production, fill-finish contract manufacturing has become a crucial area of focus ...

Any company looking to work with a CDMO should begin by defining its own product’s development requirements. For example, a ...

announces that it has obtained regulatory approval from the EMA (European Medicine Agency) to produce cell therapy treatments for the European market. C3i, therefore, obtains a certificate of GMP ...

Atara Biotherapeutics, Inc. (Nasdaq: ATRA), a leader in T-cell immunotherapy, leveraging its novel allogeneic Epstein-Barr ...

The report, released at Global Pharmaceutical Quality Summit in Mumbai, draws comparison of incidences of ‘official action indicated' after USFDA inspections a decade apart.

Enrollment completed in VIRAGE Phase 2b clinical trial of VCN-01 in metastatic pancreatic ductal adenocarcinoma (PDAC); topline data expected ...

India’s pharmaceutical sector, the world’s largest supplier of generic medicines, is poised for a new era of growth with ...

McKinsey report says Indian pharma rose to global prominence led by export boom & improved compliance: Shardul Nautiyal, Mumbai Saturday, March 1, 2025, 08:00 Hrs [IST] McKinsey & ...