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Pharmaceutical Coating Drying Process Articles & Analysis

24 articles found

The Multi-faceted Application of Enzymes in Modern Biotechnology

The Multi-faceted Application of Enzymes in Modern Biotechnology

Enzymes have always served as the silent drivers behind countless biological processes, but their role in applied science has never been more crucial. As modern biotechnology advances, the application of enzymes in industrial biotechnology, medical diagnostics, and sustainable manufacturing has evolved into a multidisciplinary field, leveraging protein engineering and synthetic biology to unlock ...

ByCreative Enzymes


How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

As spring arrives, so does a renewed focus on cleaning, quality, and process validation in pharmaceutical facilities. Whether it’s a routine seasonal turnover or preparation for ramped-up production cycles, spring is a critical time in the pharmaceutical industry for equipment maintenance, cleaning validation, and ensuring product purity. Behind every cleanroom, batch reactor, or ...

ByFluorostore


Spring Clean Starts in the Lab: How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

Spring Clean Starts in the Lab: How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

As spring arrives, so does a renewed focus on cleaning, quality, and process validation in pharmaceutical facilities. Whether it’s a routine seasonal turnover or preparation for ramped-up production cycles, spring is a critical time in the pharmaceutical industry for equipment maintenance, cleaning validation, and ensuring product purity. Behind every cleanroom, batch reactor, or filtration ...

ByFluorostore


Unleashing the Potential of Bacterial Genome Editing: A Gateway to the Future

Unleashing the Potential of Bacterial Genome Editing: A Gateway to the Future

Technological advancements and innovative research have continuously led to the discovery and development of new methodologies in the field of biological and medical sciences. One such breakthrough discovery is bacterial genome editing, which opens a new world of opportunities and challenges in the field of biotechnology and genomics. Understanding Bacterial Genome Editing Bacterial genome ...

ByCreative Biogene


Unleashing the Potential of Bacterial Genome Editing: A Gateway to the Future

Unleashing the Potential of Bacterial Genome Editing: A Gateway to the Future

Technological advancements and innovative research have continuously led to the discovery and development of new methodologies in the field of biological and medical sciences. One such breakthrough discovery is bacterial genome editing, which opens a new world of opportunities and challenges in the field of biotechnology and genomics. Understanding Bacterial Genome Editing Bacterial genome ...

ByCreative Biogene


Leveraging Automation in Pharmacy Packaging

Leveraging Automation in Pharmacy Packaging

The pharmaceutical industry has always been at the forefront of innovation, and automation has played a vital role in driving the industry forward. With an increasing demand for pharmaceutical products, there has been a need for faster and more efficient packaging solutions on a commercial scale. Pharmacy packaging automation is an effective solution to meet this demand. Read on to explore ...

ByPlastic Ingenuity


Controlling Pharmaceutical Coating & Drying Process Emissions - Case Study

Controlling Pharmaceutical Coating & Drying Process Emissions - Case Study

The Challenge Originally published in Tablets & Capsules Magazine Capturing and destroying harmful emissions from pharmaceutical processes can be challenging. It’s not because the volatile organic compounds (VOCs) are difficult to destroy using catalytic or thermal techniques. It’s because their concentrations can be so high. These ...

ByAnguil Environmental Systems, Inc.


Understanding API-Excipient Interactions in Pharmaceutical Formulations   

Understanding API-Excipient Interactions in Pharmaceutical Formulations  

Pharmaceutical formulations consist of active pharmaceutical ingredients (APIs) and excipients. Appropriate excipient selection is critical to the final quality of pharmaceutical products. When designing pharmaceutical preparations, the choice of excipients should not only consider the dosage form factors and excipient functions but also the interaction and compatibility between APIs and ...

ByCD Formulation


A New Challenge for Quality Experts - the Data Quality Concept

A New Challenge for Quality Experts - the Data Quality Concept

Abstract The role of quality systems in pharmaceutical organizations has grown faster than any other function during the last 15 years. During this period, a small group dedicated to traditional Compliance grew and expanded to include Quality Experts in areas such as validation, product release, operations, sterility assurance, and other specialized functions. Creating a deeper quality connection ...

ByParticle Measuring Systems (PMS)


Usage of Smart Device in the Healthcare Industry

Usage of Smart Device in the Healthcare Industry

A smart device in the 21st century is an essential tool that bridges the gap between humans no matter where they are in the world. With the constant evolution of technology, we are now able to build a connection and socialise in astonishing ways we would have never imagined decades ago. Though mobile phones are the most common smart devices that people are aware of, modern technology is ...

BySky Labs


What Are the Cytokines?

What Are the Cytokines?

Cytokines are a class of small molecule proteins secreted by cells that mediate and regulate immune processes, and they act in an autocrine, paracrine and endocrine manner. More than 200 types of human cytokines have been identified, which can be generally classified into interleukins, interferons, tumor necrosis factors, colony-stimulating factors, chemokines, growth factors, etc. according to ...

ByCreative Proteomics


HEPA filter emission monitoring for pharmaceutical powder processing - Case Study

HEPA filter emission monitoring for pharmaceutical powder processing - Case Study

Material: Powder Dust Loadings: Less than 0.5 mg/m3 Installation: LEAK ALERT 65-02 post vacuum pump Filter Type: HEPA (High efficiency particulate air) ...

ByENVEA


Pharmaceutical HVAC Systems: Precision Process Control - Case Study

Pharmaceutical HVAC Systems: Precision Process Control - Case Study

The Challenge: Two separate pharmaceutical packaging firms required unique air conditioning technology. In one case, a returning customer requested precisely controlled conditions to provide an exact level of uniform drying for fluid bed dryers used by the manufacturer to coat capsules, pills and caplets. The second pharmaceutical company required a single packaged system containing ...

ByAir Innovations


Clarification for vaccines

Clarification for vaccines

Clarification for vaccines – the economic and efficient removal of cell debris and negatively charged molecules with FILTRODISC BIO SD and FILTRODISC R2U depth filter modules. The purification of vaccines is a critical step during their complex production process. Cells and cell debris, as well as unwanted contaminants such as host cell proteins (HCPs) and nucleic acids need to be removed, ...

ByFiltrox AG


It is possible for pharmaceutical quality to be the combination of Quality by Design (QbD) and current Good Manufacturing Practices (cGMP)?

It is possible for pharmaceutical quality to be the combination of Quality by Design (QbD) and current Good Manufacturing Practices (cGMP)?

The following is the summary of a noteworthy discussion from the 2019 GMP Academy Master Course – Particle Measuring Systems, Rome, Italy The first GMP Academy Master Course took place from November 26 – 28 at Particle Measuring Systems (PMS) in Italy. International experts met to share their knowledge and expertise of regulatory requirements and practical applications pertaining to ...

ByParticle Measuring Systems (PMS)


Elimination of active pharmaceutical ingredients (APIs) and other problematic components from wastewater

Elimination of active pharmaceutical ingredients (APIs) and other problematic components from wastewater

Pharmaceuticals and their metabolites are detected on an increasing scale in the aquatic environment. The pharmaceuticals (such as drugs) mostly get into the surface and drinking water through the excretions of humans and animals; however, the wastewater of pharmaceutical production facilities can also be contaminated with active ingredients. The production of pharmaceuticals takes place in two ...

ByEnviroChemie GmbH - part of the EnviroWater Group


Microbial Survival in Compressed Gases Under Fast Decompression to Normal Atmospheric Conditions

Microbial Survival in Compressed Gases Under Fast Decompression to Normal Atmospheric Conditions

Introduction and Goal Compressed gases are broadly used in medicinal production facilities. A variety of different gases can be introduced into the process at various stages of a product’s manufacture for different reasons. Compressed gases such as air, nitrogen, and carbon dioxide are regularly used in cleanrooms and are frequently employed in purging or overlaying. The cleanliness of ...

ByParticle Measuring Systems (PMS)


Guidelines For Cleaning Pharmaceutical Processing Equipment

Guidelines For Cleaning Pharmaceutical Processing Equipment

Cleaning pharmaceutical processing equipment is challenging. Cleaning methods, soils present, type of manufacturing equipment, surfaces cleaned, choice of cleaning detergent and temperature should all be considered when setting up a cleaning procedure. Cleaning validation methods are required. The entire cleaning process must be standardized and documented according to the FDA’s cGMP ...

ByInternational Products Corporation


Issues Brought Up During BC-CM Producers Group Meeting Featured By Inside EPA Article

Issues Brought Up During BC-CM Producers Group Meeting Featured By Inside EPA Article

On January 13, 2017, slides from the B&C® Consortia Management’s (BC-CM) NMP Producers Group Meeting with the Office of Management and Budget were discussed in the Inside EPA article “Chemical Makers Cite TSCA Listing In Call For EPA To Drop NMP Proposal.” But representatives from Bergeson & Campbell on behalf of NMP producers in a Dec. 5 meeting with EPA and OMB ...

ByBergeson & Campbell, P.C.


Controlling Pharmaceutical Coating & Drying Process Emissions

Controlling Pharmaceutical Coating & Drying Process Emissions

Pharmaceutical operations, however, typically require customized emission control systems to handle the high VOC concentrations that emanate from tablet coating, fluid-bed processing, and tray drying. Often the concentrations reach the explosive range, which means the emissions must be diluted before they’re introduced to ...

ByAnguil Environmental Systems, Inc.

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