Our latest life science news | ProductLife Group

22 january 2025

Bridging Regulatory and Technical Challenges in Continuous Manufacturing of Biologics

21 january 2025

Regulatory Submission Strategy for Approval in Europe

16 january 2025

Comprehensive Nitrosamine Risk Assessment: ProductLife Group's Expertise

14 january 2025

India and China: Supplier Audits – Expertise at Your Service!

07 january 2025

International Recognition Procedure (IRP)

10 december 2024

Transforming MedTech: The Impact of the EU AI Act

05 december 2024

Understanding FDA Drug Master Files: An Overview

28 november 2024

A Comprehensive Guide to eCTD Baseline Submission

19 november 2024

Continuous Manufacturing in Pharmaceuticals: Critical Factors and Success Strategies Part 2