GSK and Oxford Collaborate to Pave the Way for Life-Saving Cancer Vaccines

A second research collaboration between SK and the University of Oxford allows analysis of cancer prevention through vaccine therapy. The GSK-Oxford immuno-anticipation program will conduct translational research by studying precancer science to better understand human cancer evolution which creates potential opportunities for new vaccines. Early research follows GSK’s commitment of up to £50m ($62.3m) across three years. Oxford University’s expertise […]

Types and SOP for Portable Fire Extinguishers Used in the Pharmaceutical Industry

The pharmaceutical industry is highly regulated, with safety being a top priority due to the handling of chemicals, flammable substances, and sensitive equipment. One essential component of workplace safety is the proper use of portable fire extinguishers. These devices play a critical role in preventing small fires from escalating into significant hazards, protecting personnel, equipment, and facilities. In this article, […]

SOP for Air Handling Units (AHU) in the Pharmaceutical Industry

The pharmaceutical industry relies heavily on precise environmental control to ensure product quality, regulatory compliance, and patient safety. Air Handling Units (AHUs) play a crucial role in maintaining cleanroom conditions, controlling temperature, humidity, and air quality in pharmaceutical manufacturing facilities. Each type of AHU is designed to meet specific operational needs and adhere to stringent Good Manufacturing Practices (GMP). This […]

Standard Operating Procedure (SOP) Determination of Residual Hydrocarbon Content in Pharmaceutical Gases

1. Purpose The purpose of this Standard Operating Procedure (SOP) is to outline the method for the determination of residual hydrocarbon content in pharmaceutical gases used in manufacturing processes. The accurate quantification of hydrocarbons ensures compliance with regulatory standards and maintains the quality of pharmaceutical products. 2. Scope This SOP applies to the analysis of residual hydrocarbon content in pharmaceutical […]

Methods and Procedures for Determination of Particulate Matter Contamination in Pharmaceutical Gases

Pharmaceutical gases play a critical role in various processes within the pharmaceutical industry. Whether used as a propellant, carrier, or active ingredient, the quality and purity of these gases are paramount. Among the many quality parameters to assess, particulate matter contamination is of utmost concern as it can compromise product quality, safety, and efficacy. This article provides an in-depth examination […]

Standard Operating Procedure for Chilled Mirror Hygrometer to Determine Moisture Content of Pharmaceutical Gases

Introduction Moisture content in pharmaceutical gases plays a critical role in ensuring product quality, safety, and compliance with regulatory standards. Accurate determination of moisture levels is vital for maintaining controlled environments and preventing potential degradation of pharmaceutical products. The Chilled Mirror Hygrometer is a highly precise instrument used to measure the moisture content of gases. This article outlines the standard […]

Methods and Procedures for Determination of Moisture Content in Gases Used in the Pharmaceutical Industry

Moisture content in gases used in the pharmaceutical industry is a critical parameter. Excess moisture can lead to undesirable chemical reactions, microbial growth, and compromised product integrity. To ensure the quality and compliance of pharmaceutical processes, gases such as nitrogen (N₂), carbon dioxide (CO₂), helium (He), and argon (Ar) must have moisture levels that meet stringent standards. This article details […]

Pharmaceutical-Grade Helium (He): Specifications, Testing Requirements, and Procedures

Pharmaceutical-grade helium (He) is a highly purified inert gas extensively used in the pharmaceutical industry for its non-reactive properties and versatility. Applications range from cryogenics to chromatography and inerting processes. Due to its critical role in ensuring the safety and efficacy of pharmaceutical products, helium must meet stringent quality and purity standards. This article outlines the specifications, testing requirements, and […]

Pharmaceutical-Grade Argon (Ar): Specifications, Testing Requirements, and Procedures

Pharmaceutical-grade argon (Ar) is a high-purity gas used in the pharmaceutical and biopharmaceutical industries for its inert properties. It is commonly employed in applications such as inerting, blanketing, and preservation, where it helps prevent oxidation, degradation, or contamination of sensitive materials. Due to its critical role, pharmaceutical-grade argon must meet stringent specifications and undergo rigorous testing. This article delves into […]

Pharmaceutical-Grade Carbon Dioxide (CO₂): Specifications, Testing Requirements, and Procedures

Pharmaceutical-grade carbon dioxide (CO₂) plays a vital role in the pharmaceutical industry, where it is used for a variety of applications, including pH control, cryopreservation, and as a propellant in aerosol products. Its quality and purity must meet stringent specifications to ensure safety, efficacy, and compliance with regulatory standards. This article explores the specifications, testing requirements, and procedures for pharmaceutical-grade […]