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   Whats new?
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August 9, 2023


HOMOGENIZATION OF CELLS & ALIQUOTATION IN SINGLE-USE BAGS

Brian Moloney

Who can relate to the situation when every cell aliquot is different? That's why
cell homogenization and aliquotation are important requirements in modern cell
biology research, relevant for scientists and laboratory staff. Scientists and
process engineers benefit from uniform cell distribution throughout multiple
single-use bioprocess containers for cell banking or other bioprocessing steps.

read more


April 12, 2023


AUTOMATED BIOPROCESSING – 7 ADVANTAGES OF AUTOMATION

Mike Marciniak

Automation is affecting various aspects of our lives, including bioprocessing.
In this article, we will explore the advantages that come with this development.

read more


April 11, 2023


DRUG SUBSTANCE VS. DRUG PRODUCT – THESE ARE THE DIFFERENCES

Michael Eder

The terms "drug substance" and "drug product" are often used synonymously,
although there are some fundamental differences between them. We will point them
out in the course of this article!

read more


April 6, 2023


BIOPROCESSING – EVERYTHING YOU NEED TO KNOW

Mike Marciniak

Bioprocessing is a fundamental technology for various aspects of our lives,
including the biopharma industry. In this article, we will provide some
interesting facts about applications, techniques and future expectations
regarding bioprocessing.

read more


March 17, 2023


MICROBIAL FERMENTATION MANUFACTURING: ADVANCES THROUGH SINGLE-USE TECHNOLOGIES

Daniel Tischler

Microbial fermentation is a powerful, flexible microbiology process used to
generate microbial cells or biomass such as proteins and enzymes for the
production of vaccines and therapeutics. There are still some challenges to
overcome. Many of these challenges in fermentation manufacturing can be solved
by replacing traditional systems with single-use technologies. 

read more


March 16, 2023


BIOPHARMA PACKAGING - REQUIREMENTS AND SOLUTIONS

Michael Eder

In this article, we will discuss the special requirements of biologicals in
terms of packaging as well as efficiency and sustainability aspects of biopharma
packaging.

read more


March 14, 2023


PRIMARY AND SECONDARY PACKAGING OF DRUG SUBSTANCES

Michael Eder

Throughout the manufacturing process of drug substances, the liquids must be
transferred frequently, such as during the upstream and downstream processing.
Safe packaging of large volume substances is of high necessity in each step.
Protection is ensured by appropriate primary and secondary packaging. This
article will provide an overview of the different types of primary and secondary
packaging materials, which are used specifically for safe handling of drug
substance. 

read more


March 14, 2023


COLD CHAIN HANDLING FOR FERMENTATION: SINGLE-USE SOLUTIONS TO LOWER COSTS

Mike Marciniak

As expert for cold chain handling in bioprocessing, Single Use Support is
providing solutions to meet challenges for safe storing and shipping associated
with right freezing and thawing methods and temperature control for long-term
storage. Their development approach leads to innovative systems that enable
manufacturers to replace manual processes with fully automated end-to-end
processes that not only push efficiency but also increase output.

read more


March 6, 2023


BIOPHARMACEUTICAL PROCESSING – HOW DISPOSABLE SOLUTIONS INCREASE SAFETY AND
EFFICIENCY

Mike Marciniak

Biopharmaceutical processing is indispensable across various fields of medicine
and life sciences. In this article, we will discover how single-use solutions
can increase efficiency and safety in biopharmaceutical processing.

read more


March 1, 2023


MEETING CGMP REGULATIONS WITH INNOVATIVE SINGLE-USE TECHNOLOGIES

Michael Mühlegger

Manufacturers in the pharmaceutical industry are required to comply with cGMP
(Current Good Manufacturing Practice). End-to-end solutions based on automated
single-use technologies are an auspicious choice for drug substance
manufacturers, given their many advantages. Their implementation in the
manufacturing process promises efficiency, high product quality, cost reduction,
and energy savings.

read more


March 1, 2023


CGMP - EVERYTHING YOU NEED TO KNOW

Michael Mühlegger

The current Good Manufacturing Practice (cGMP) regulations - originated and
checked by the FDA - apply to companies operating in pharmaceutical, biotech, or
med tech industries. They require the latest standards in terms of production,
manufacturing, and packaging and thereby ensure pharmaceutical quality meaning
quality in manufacturing processes and patient safety as the ultimate goal. The
detailed requirements, importance of cGMP, and how companies can best meet the
cGMP regulations, are discussed in the following.

read more


February 28, 2023


SHIPPING PHARMACEUTICAL LIQUIDS AND ITS CHALLENGES

Daniel Tischler

The global distribution of pharmaceuticals is complex and demanding, requiring
precise handling and storage of sensitive products. With the rise of
personalized medicine and the increasing globalization of the industry, the need
for safe and efficient shipping and supply chain has never been more important.

read more

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