Close
Novotech
Jabsco PureFlo 21 Single Use

Research reveals costly implementation is the biggest barrier to serialization compliance

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Related stories

Integrated Inspection Systems for Leak Detection in Pharma

The pharmaceutical industry is increasingly moving toward a more holistic approach to quality control by combining various inspection technologies into a single, unified platform. Integrated inspection systems for leak detection in pharma offer a multi-faceted solution that simultaneously addresses cosmetic defects, particulate contamination, and container closure integrity. By merging high-speed visual cameras with sensitive high-voltage leak detection modules, these systems provide a comprehensive assessment of every unit, ensuring that each dose of medication is contained within a perfectly sealed and sterile environment. This integration not only reduces the risk of secondary contamination but also significantly improves the overall efficiency and reliability of the manufacturing process.

Advancing Pharma Quality with HV Leak Detection Tools

Maintaining the highest standards of pharmaceutical quality is a fundamental requirement for the safe delivery of injectable medications. The development of advancing pharma quality with HV leak detection tools represents a major leap forward in the deterministic testing of container closure integrity. By utilizing sophisticated sensors and high-voltage electrical fields, these tools can detect microscopic structural defects that would otherwise compromise the sterility of life-saving products. This high-sensitivity approach significantly enhances the accuracy of the inspection process, providing manufacturers with a robust solution for ensuring packaging integrity and regulatory compliance.
- Advertisement -

According to new industry research more than half (54%) of industry professionals believe that the cost of implementing serialization is the greatest hurdle to compliance.

The research, conducted by serialization software provider, SEA Vision and life sciences technology firm, Zenith Technologies, highlighted that the substantial investment required to implement a serialization solution is cause for concern ahead of regulatory deadlines in the US and Europe.

A further 33% of survey respondents stated the implementation process would be a drain on internal resource. Others (31%) cited tight timescales as a pain point, a statistic that is further supported by the announcement that the FDA will delay the active enforcement of the Drug Supply Chain and Security Act (DSCSA) due to a lack of readiness across the industry. Commenting on the research, Carlos Machado, serialization director at SEA Vision US said: “The new regulations in the EU and the US represent a substantial upfront investment for companies across the supply chain and many smaller players are struggling to implement a suitable process as a result.

“The resource required in terms of cost and manpower is a notable barrier to compliance, but added to that, the time it takes to develop a solution has been gravely underestimated by a large part of the industry. Many (37%) of our survey respondents expressed concerns surrounding the potential disruption to product supply as a result of technical issues and downtime, which clearly demonstrates the impact serialization could have at an operational level.

Consolidation across the outsourcing space has been prevalent for some time now and serialization is undoubtedly driving smaller companies to consider partnerships to offset a lack of manpower and budget. However, 36% also believed that there was a knowledge gap in their existing teams surrounding serialization, making external expertise vital to ensuring compliance. Machado continued: “With time and cost becoming a growing concern across the pharmaceutical industry, it’s no surprise that smaller partners, particularly contract manufacturers, are looking to consolidate to expand their internal resource.

“In addition to consolidation and a growing trend to outsource serialization requirements, it is also likely that we will see an increased reliance on third party implementation specialists with the knowledge and expertise to effectively introduce the necessary changes and also help companies realise the wider business benefits that can be achieved. For example, implementing serialization can also help to improve line performance and overall equipment effectiveness (OEE).”

In 2016, SEA Vision and Zenith Technologies formed a global partnership to support pharmaceutical companies with the impending challenge of installing and integrating serialization across drug manufacturing sites.The collaboration brings together Italian-based SEA Vision’s serialization system along with global Zenith Technologies’ ability to integrate systems and deliver ongoing technical support at a local level.

For further information, please visit:
http://www.seavision-usa.com and http://www.zenithtechnologies.com/
or contact Carlos Machado directly at cmachado@seavision-usa.com

Latest stories

Related stories

Integrated Inspection Systems for Leak Detection in Pharma

The pharmaceutical industry is increasingly moving toward a more holistic approach to quality control by combining various inspection technologies into a single, unified platform. Integrated inspection systems for leak detection in pharma offer a multi-faceted solution that simultaneously addresses cosmetic defects, particulate contamination, and container closure integrity. By merging high-speed visual cameras with sensitive high-voltage leak detection modules, these systems provide a comprehensive assessment of every unit, ensuring that each dose of medication is contained within a perfectly sealed and sterile environment. This integration not only reduces the risk of secondary contamination but also significantly improves the overall efficiency and reliability of the manufacturing process.

Advancing Pharma Quality with HV Leak Detection Tools

Maintaining the highest standards of pharmaceutical quality is a fundamental requirement for the safe delivery of injectable medications. The development of advancing pharma quality with HV leak detection tools represents a major leap forward in the deterministic testing of container closure integrity. By utilizing sophisticated sensors and high-voltage electrical fields, these tools can detect microscopic structural defects that would otherwise compromise the sterility of life-saving products. This high-sensitivity approach significantly enhances the accuracy of the inspection process, providing manufacturers with a robust solution for ensuring packaging integrity and regulatory compliance.

Sustainable Nutraceutical Ingredients Shaping the Future

The Shift Toward Sustainable Ingredients One of the most significant...

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Translate »