Pharmaceutical Technology

Pharmaceutical Freeze Drying: GMP Compliance and EU Annex 1

Pharmaceutical freeze drying is essential for producing stable, high-quality medicines. However, pharmaceutical manufacturers must meet strict Good Manufacturing Practice (GMP) requirements while improving energy efficiency and maintaining product quality.

Bowie-Dick Test: Complete Guide to Steam Sterilization and Autoclave Air Removal

The Bowie-Dick test is a routine performance check for fractionated vacuum autoclaves. It confirms that the autoclave can remove air effectively and allow saturated steam to penetrate porous loads evenly.

FUTURE-PROOF TECHNOLOGIES FOR THE PHARMACEUTICAL INDUSTRY – EVENT RECAP

The event brought together pharmaceutical manufacturers, industry professionals, technology experts, and business partners to exchange insights on the latest developments shaping the future of pharmaceutical manufacturing in Vietnam.

RSA Premium 3-in-1: Advancing cGMP pharmaceutical combined sterilization technology

In sterile pharmaceutical manufacturing, sterilization is no longer simply a final support step. It is a critical process that directly affects patient safety, regulatory compliance, product quality, and production efficiency.
cargo ship port with a highway over it representing international trade and business solutions

Future-Proof Technologies for Pharmaceutical Industry 2026

The pharmaceutical industry is entering a new era of innovation, where digitalization, sustainability, automation, and regulatory excellence are transforming the way medicines are developed and manufactured.

TTS/C Serialization and Aggregation Line

From integrated weight control with automatic rejection to data matrix code printing and manual aggregation management, this technology is designed to ensure maximum compliance and security at every stage of packaging.

Blow-Fill-Seal Case Study: Pioneer Enhances BFS Inspection with HEUFT Technology

Pioneer Co. for Pharmaceutical Industries, one of the largest blow-fill-seal (BFS) manufacturers in the Middle East, has significantly strengthened its quality assurance processes by implementing advanced HEUFT spotter II BFS inspection systems.

Elevating Quality Control in Vietnam with Wilco & Melchers

In today’s high-precision manufacturing environment, ensuring product quality and safety is critical. Wilco’s advanced vision inspection systems, exclusively represented by Melchers Vietnam.

EU GMP Annex 1 Compliant Inspection of BFS Bottles

EU GMP Annex 1, issued by the European Medicines Agency (EMA), regulates the manufacture of sterile medicinal products. The latest revision (2022) became mandatory on 25 August 2023.

GMP Biorefinery Engineering Project Advances Thailand’s Biotechnology Ambitions

Thailand is accelerating its transformation into a regional biotechnology hub with the development of a GMP Biorefinery Pilot Plant at the Eastern Economic Corridor of Innovation (EECi).