Newsletter | December 5, 2023

12.05.23 -- Leveraging An Application Managed Services (AMS) Provider For Pharma/Biotech Serialization Systems

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FEATURED EDITORIAL

Leveraging An Application Managed Services (AMS) Provider For Pharma/Biotech Serialization Systems

With the expansion of serialization requirements, including the need for Drug Supply Chain Security Act compliance, many pharma/biotech companies are turning to serialization technology systems to help them manage those specifications. This article shares the key benefits of leveraging an application managed services (AMS) provider as well as key considerations for selecting a provider.

INDUSTRY INSIGHTS

Increasing Dwell Time In Pharmaceutical Tablet Manufacturing

Many types of punches and dies are available to help compress difficult drug products. Explore the benefits as well as some drawbacks of using extended head flats.

Selecting An Alternative Coating Technology For Prefillable Syringes

The challenges of silicone-oil lubrication and the growing trend for more viscous, protein-based drugs are now leading pharma and biotech companies to investigate alternative solutions.

A Micronization Method Enabling The Formulation Of Biopharmaceuticals

Discover how applying lyophilization-based micronization methodology at a small scale helps to support challenging formulation development projects.

Advantages Of A CDMO With Internal Biosafety Testing Capabilities

Learn about three biosafety testing methods that are commonly applied: in vitro adventitious virus (IVV), species-specific virus testing such as minute virus of mice (MVM), and mycoplasma.

An Introduction To Laminar Airflow Technology In Aseptic Processing

Explore the vital role that laminar airflow technology plays in meeting sterile integrity standards and minimizing contamination risks in pharmaceutical cleanrooms.

Solving Powder Handling Challenges With Single-Use Technology

Here, we address five critical questions to consider when selecting single-use containment equipment for your powder transfer systems.

5 Ways Pharmaceutical Manufacturers Can Improve Productivity And Quality

With expectations that drugs will be produced faster and more inexpensively, how can a pharmaceutical manufacturer be prepared for what’s on the horizon?

Applications For High Voltage Leak Detection You Might Not Be Aware Of

Learn in detail about high voltage leak detection (HVLD), packaging applications that can be inspected with HVLD, and how to determine the best leak-testing method for your application.

Validated LC-MS/MS Method For The Determination Of Copanlisib

Review the study’s findings on a validated LC-MS/MS method for quantifying copanlisib from a mouse DBS and its potential for enabling desirable sensitivity, accuracy, and precision.

Achieving Speed And Scale With Optimized Synthesis Solutions

By working to select the right synthesizer and prioritizing automation, organizations can realize optimal coupling efficiency and increased productivity for oligonucleotide drugs.

Why Flexible Space Is Key In Getting Therapies To Market Faster

In the race to get new drugs from the research stages to pharmacy shelves, next-generation lab space can be the catalyst for success.

Balancing Cost Efficiencies In The Drug Development Process

Cost efficiencies and expertise go hand in hand, with companies often outsourcing or partnering primarily to gain access to manufacturing know-how.

Clear Hoods To Protect Biopharmaceutical Facility Employees

See how a clear hood for biopharmaceutical facility employees improved safety and performance while promising economic savings.

Better Therapeutic Outcomes From Better Drug Delivery

Innovative drug-eluting implants, inserts, and transdermal films delivering biologics and small molecules can meet the goals of patient-centric therapies, improved medicine, and better healthcare economics.

Advantages And Disadvantages Of Sample Preparation For Small Molecules

Sample preparation for small molecules involves three primary modes, each presenting its own set of advantages and disadvantages.

Understanding The Oligonucleotide Synthesis Process

Synthetic oligonucleotides are primarily used in therapeutics, as well as in diagnostic kits and PCR primers. This animation explains the repetitive four-step cycle of the oligonucleotide synthesis process.

Nanoforming: The Patient- And Planet-Centric Approach

By reducing drug particle size, nanoforming can create new opportunities, from increasing bioavailability to enabling sustained drug delivery. Discover the potential benefits supported by case studies.

Improved Design And Production Of Bispecific Therapeutics

See how bispecific pairing technology uses a close-to-nature design solution to deliver highly accurate heavy-light chain pairing efficiencies and improved manufacturability.

SOLUTIONS

Small Molecule APIs Made With Compelling Science

Contract Packaging Services For Probiotics

Self-Contained Biological Indicator For Monitoring Steam Sterilization

Surfactant Analysis Services

Clean Process Products For Critical Environments

Pharmaceutical Helium Leak Testing Services

Used Shionogi Qualicaps Pharmaceutical Capsule Filling Machine

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