Designed to expedite gene to GMP manufacturing in as little as 9 months.

Systech, a provider of pharmaceutical serialization and traceability services, launched two new integrated packaging ...

For biological drug substances, the effect of thawing and shear on product quality are evaluated. Fill interruption studies ...

Section 232 drug tariffs are expected to accelerate the shift toward domestic manufacturing, but smaller drugmakers may find ...

Strategic investments strengthen resilience and service capabilities for innovative injectable therapies Ravensburg, ...

Christy Eatmon, Global Steriles SME, Thermo Fisher Scientific, Pharma Services Group, discusses how Thermo Fisher Scientific ...

Alcami, a CDMO, has appointed biologics industry veteran Will Isom as Vice President of Laboratory Services Sales. The ...

This week on "The Friday Brief," we wrap up our 25th year of the Contract Pharma Contracting & Outsourcing Conference.

The approved variation enables Upperton to commence GMP manufacture of sterile investigational medicinal products from the purpose-built facility, expanding the company’s integrated development and ...

The first-ever CPHI Sustainability Summit brings together key stakeholders from the pharmaceutical and healthcare industries ...

Decisions around trial design, regulatory strategy, and manufacturing planning ultimately determine whether a therapy reaches patients.

This week on "The Friday Brief," companies put down roots on both sides of the Atlantic, expanding their capabilities in a number of areas.