How to incorporate highly potent drug products into your facility

How to incorporate highly potent drug products into your facility

There are many benefits to adding highly potent drug products to your portfolio, including increasing demand and generating potentially higher profit margins. Making the decision to incorporate highly potent drug products into your manufacturing facility can be a challenging process.

Read More
A large chiller outside, which could be made more efficient with an ice storage system

How biopharma facilities can use ice in a glycol chiller system

Ice storage, coupled with a glycol chiller, can provide benefits that other options can’t.

Read More
Oral solid dose tablets on a continuous manufacturing line

Continuous OSD manufacturing—a technology update

Continuous oral solid dosage manufacturing is a transformational processing platform that is here today and is here to stay. Although the industry is working on harmonization and some level of standardization of the platforms, continuous manufacturing is not a one-size-fits all offering.

Read More
Closing the deal: Understanding when to close your process

When to close your pharmaceutical process

Too often, the term “closed process” is thrown around without an understanding of the salient issues. Pharmaceutical process closure can certainly provide many benefits, but there are various impacts and requirements depending on the ultimate goal and the specific process you are trying to close.

Read More
Can’t hack it? Why pharma should heed the growing threats to cyber security

Cybersecurity considerations for pharmaceutical companies

Who would want to hack a programmable logic controller? Is cybersecurity really that important for pharma companies?

Read More
Oral solid dose tablets on a continuous manufacturing line

Continuous OSD manufacturing and patient impact

FDA approved oral solid dosage (OSD) products are improving, changing and enhancing lives, via the use of a continuous manufacturing platform. 

Read More
Solving biopharma design challenges with computational fluid dynamics part one: Designing a mixing tank with high-performance computing in the cloud

Solving biopharma design challenges with computational fluid dynamics

Computational fluid dynamics and cloud computing can make complex models more cost-effective and less time-consuming.

Read More
Passing through the barrier

Passing through the barrier

Over the past decade, aseptic filling isolators have improved patient safety by use of barriers to isolate the point of filling from personnel. This industry-wide movement creates opportunities to further increase patient safety by minimizing viable and nonviable risks to the aseptic fill.

Read More
Strip the strip curtains

Strip the strip curtains in aseptic cleanrooms

Like most things, improvement happens naturally over time with the application of knowledge and the advancement of technology. This is particularly true for aseptic cleanrooms and even more so with respect to strip curtains. As cleanroom technology has evolved, we’ve developed a better understanding of how to—and how not to—maintain an aseptic environment.

Read More
To outsource or not to outsource? That is the question: How to ensure your CMO stacks up

How to choose a contract manufacturing organization

The age-old debate of whether to outsource production to a contract manufacturing organization (CMO) remains for mature, emerging and virtual biopharmaceutical companies.

Read More

Pharmaceuticals Newsletter

Be the first to receive The Next Pharmaceuticals Insights.
  • This field is for validation purposes and should be left unchanged.