Newsletter | June 7, 2024

06.07.24 -- EMA Updates Guidance On Inhalation And Nasal Product Quality

FEATURED EDITORIAL

EMA Updates Guidance On Inhalation And Nasal Product Quality

The EMA has issued a new draft guideline, “Guideline On The Pharmaceutical Quality Of Inhalation And Nasal Medicinal Products.” The public comment period ends Oct. 31.

INDUSTRY INSIGHTS

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?

How Your Stainless-Steel Column Is Like A French Press

Understanding how purification columns help operators to better conceptualize the process enables greater understanding and troubleshooting.

The Execution Stage Of Technology Transfer

What are the key elements in the readiness stage of a technology transfer that are critical to your success? Explore Process Performance Qualification (PPQ) and the execution stage of PDA TR-65.

Extended Head Flats Increase Dwell Time

Explore the extended head flat and how this punch modification can improve the compression of difficult formulations.

Unstoppable Critical Cleaning To Increase Pharmaceutical Throughput

Process optimization is key to achieving effective pharmaceutical and cosmetic critical cleaning. Learn how manufacturers can improve cleaning efficiency and ensure product safety.

Diagnose Absorption Risks To Improve Preclinical And Clinical Outcomes

Physiologically based pharmacokinetic modeling is a powerful tool for clinical trial design that can be leveraged alongside early development experiments to reduce costs and accelerate timelines.

Real-Time Viable Particle Detection For Definitive Root Cause Investigation

Investigations into viable air excursions are difficult to perform using traditional methods. Discover why a real-time viable particle counter is key to providing process improvement.

Pediatric Patient Considerations During Dose Development

Specific dosing guidelines and acceptable dosage forms for pediatric patients must be developed to optimize therapeutic efficacy and limit and prevent serious adverse side effects.

Alkaline Stability Of Modern Protein A Chromatography Resins

Explore results from a resin lifetime study with over 150 cycles, using clarified cell harvest in every cycle, which has been performed to evaluate the alkaline stability of three protein A resins.

Ensuring The Efficacy Of Probiotic Products

Without proper handling and packaging, the efficacy of probiotics can be compromised at any point in the packaging, storage, and transportation process, impacting shelf life and effectiveness.

Mixing Technology Considerations For The Cannabis And CBD Industries

Explore an array of mixers and mixing technologies that can help you throughout the cannabis product manufacturing process.

Three Ways Manufacturing Excellence Drives Value For Life Sciences

Check out three ways Honeywell’s Manufacturing Excellence Platform delivers value in terms of costs, revenue, and risk.

SOLUTIONS

Technology To Overcome Absorption Hurdles And Solubility Limitations

Disinfectants And Solutions For Critical Environments

Glove Box To Minimize Purge Time And Maximize Inert Gas Savings

An HPLC System For An Efficient And Productive QC Lab

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