Effect of Gum on in Vitro Dissolution of Powder for Oral Suspension

About the Author

Vice President

Itaan Pharma

Dr. Ajay Babu Pazhayattil is a seasoned professional who has led technical operations, quality assurance, regulatory compliance risk mitigation, and remediation projects. He has conceived...

Amol Dattatreya Galande

Head of the Process Development Laboratory

Lupin Formulation Site

Amol Dattatreya Galande is a pharmaceutical postgraduate (MPharm) with around 18 years of industry experience in formulation development, quality assurance, and technical operations. He has...

Sudhakara Rao Badabhagni

Pharmaceutical Product Development Professional

Sudhakara Rao Badabhagni is a pharmaceutical product development professional with extensive experience in formulation development of finished dosage forms for global markets. He has worked...

Technical

Selection Criteria for Pharmaceutical Containment Equipment

1 March 2024

Pharmaceutical manufacturing facilities produce a variety of products, including highly potent products that require safety measures to prevent adverse health effects on patients and operators. To ensure safety, these facilities use containment equipment to minimize the risk of contamination. This article presents criteria for selecting containment equipment, considering both...

Technical

A Sustainable Approach to Steam Quality Management

1 March 2024

The world is beginning to grasp the huge challenge of achieving net-zero carbon emissions, or carbon neutrality, by 2050. Many countries have committed to achieving this ambitious goal. As a major global industry, the pharmaceutical sector has a significant role to play. For thermal energy–intensive industries, such as pharmaceutical manufacturing, the long-term future options to maintain...

Technical

Concluding Compliance Challenges with Validation 4.0

13 March 2024

As the pharma industry moves to an ambitious Validation 4.0 paradigm, computerized systems play a pivotal role in enabling the rapid transition. Innovation and agility in computerized system validation (CSV) received a strong push in the second half of 2022 with the publication of the FDA draft guidance on “Computer Software Assurance for Production and Quality System Software”

About the Author

Facilities of the Future: Meeting the Demands of Breakthrough Therapeutics

Emerging Leader Hacker to GAMPer in 10 Weeks

New Initiative Seeks to Back up ICHs Harmonization Mission

Data Science-Assisted Biopharmaceutical Tech Transfer and Process Characterization

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