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Editorial Archive

Without an End-to-end Review of R&D Processes, Efficiency Drives will Stall

The life sciences industry is compelled to transform efficiency across Regulatory Affairs, Quality and Pharmacovigilance/ Drug Safety functions as part of a drive to...
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Editorial Archive

We Need to Speak the Same Language: Computer System Validation in the Pharmaceutical Industry from the Supplier’s Perspective

In regulated industries such as pharmaceuticals, cosmetics, and food production, the computer system validation plays a pivotal role in ensuring compliance with the ...
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Editorial Archive

Covalent Drug Discovery: Challenges, Advances, and Success Stories

Covalent inhibitors possess a functional group that reacts with a nucleophilic residue on a target protein to form a bond that inhibits the protein’s function. Histo...
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Editorial Archive

Grappling with the Grey Zones in EMA Computerised Systems and Electronic Data Implementation

The integration of computerised systems and electronic data standards continues to play a vital role in the conduct and management of clinical trials as well as in e...
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Editorial Archive

Innovations in API Manufacturing of Small Molecule Drugs

Throughout the years, innovation has been the driving factor of many industries, allowing them to stay viable. This is also the case for the pharmaceutical industry,...
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Editorial Archive

Combination Filling: The Trend Towards Machine Customisation

What is Combination Filling?Combination filling refers to the process of placing two or more active ingredients within the same capsule. These ingredients can be in ...
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Editorial Archive

Ensuring a Smooth Transition: Tech Transfer Strategies for Monoclonal Antibody Drug Products in Late-phase Clinical and Commercial Launch

The successful transfer of a monoclonal antibody (mAb) drug product from late-stage clinical development to commercial-scale manufacturing is a pivotal milestone in ...
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Editorial Archive

Maintain Sterile Pharmaceutical Production with Uninterrupted Power Supply

Today’s pharmaceutical manufacturers face a myriad of challenges, including access to constant power supply. Power interruptions, fluctuations and outages are an unf...
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Editorial Archive

EVERIC® pure – The Safe Option Right from the Start: A Drug Containment Platform to Streamline Drug Development

The Wrong Container Choice – A Threat to Patient Safety and Time-To-Market A common situation is that pharma companies select a certain primary packaging containe...
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Editorial Archive

Labelling and Serialisation to Comply with the EU MDR

The deadline for ensuring compliance with the European Union’s Medical Device Regulations (EU MDR) is looming. These new, stricter regulations are aimed at improving...
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