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Pulsed X-Ray Technology & Smart Optics for a total inspection of pre-fillable syringe cannulas and needle shields
22 October 2020
Pulsed X-Ray Technology & Smart Optics for a total inspection of pre-fillable syringe cannulas and needle shields

The pulsed X-ray detection module from HEUFT identifies numerous safety and integrity defects of pre-fillable syringes after the caps have been applied with unrivaled low radiation. The HEUFT Syringer detects non-conformities that would normally be invisible to a camera system such as needle shields (both SNS & RNS) pierced by the hypodermic needle, deformed cannulas or incorrectly assembled, defective or leaking luer-lock screw adapters and tamper evident closures of disposable syringes.


The compact detection unit can be enhanced with innovative smart optics for detecting needle hooks which complement the unique pulsed X-ray technology for a careful and precise pre-fillable syringe inspection. An intelligent color sensor camera, developed by HEUFT, examines the tiny needle tips from above before the protective covers have been added. The special light dispersion of the adaptive LED lighting used for this purpose ensures that even the smallest faults become visible.


The HEUFT Syringer is extremely compact and very easy to integrate into packaging machines for such pre-fillable injection instruments.
During this Webinar, Information will be shared about the Heuft Syringer such as design features, functionality, implementation, and benefits of using the HEUFT Syringer to assure only quality pre-filled syringes reach the market.
 

BENEFITS OF ATTENDING AND WHAT YOU WILL GAIN
• Cannula Brand protection from FDA recalls
• patient protection from faulty products
• pulsed X-Ray technology
• design features, functionality, and implementation of the Syringe
• Benefits of Cannula inspection

WHO SHOULD ATTEND
• Quality Managers
• Heads of Quality
• Manufacturing/Operations Managers
• Heads of Manufacturing/Operations
• Heads of Fill-Finish
• Fill-Finish Manager
• R&D scientists
• Formulation scientists
• CMC regulatory
• Packaging engineers
• Engineers and Managers in Device Development and all other technical functions surrounding syringe systems
• Clinical and commercial Drug Product Manufacturing
• Formulation scientists
• Laboratory scientific staff and managers
• Parenteral manufacturing staff
• Sterility Quality Assurance
• Regulatory affairs scientists
• Pharmaceutical packaging component manufacturing staff
 

FEATURED SPEAKERS

Dan  McKee

Dan McKee

General Manager, HEUFT USA Inc
Ronald Turn

Ronald Turn

Pharmaceutical Sales Engineer, HEUFT USA Inc

Dan McKee

General Manager, HEUFT USA Inc
Dan  McKee

Dan McKee is the General Manager of HEUFT USA. He has spent 25 years working with high-speed quality control inspection equipment in the packaging industry. In doing so, he’s become well versed in non-destructive techniques for testing a wide variety of package attributes using technologies as diverse as x-ray imaging, capacitive gauging, inductive profiling, and various vision techniques. His responsibilities have included commissioning inspection devices within a wide variety of production environments, specifying devices to satisfy customers’ application conditions and working with R&D to customize equipment to conform to his customers’ unique challenges. Dan now leads HEUFT’s sales and service organization for the United States and Canada.
Dan Received his BSEE from the Illinois Institute of Technology in 1993, and a Masters of Engineering Management (MEM) in 2001 from Northwestern University.
 

Ronald Turn

Pharmaceutical Sales Engineer, HEUFT USA Inc
Ronald Turn

Ronald Turn joined Heuft USA in 2019 as the Pharmaceutical Sales Representative. Ron has spent the past 10 years in a technical sales roll selling different varieties of Capital Analytical Research Instrumentation to the Pharmaceutical, Biotech, Chemistry, and Life Sciences industries. Ron also has worked for two major Pharmaceutical companies as an Analytical Chemist. With the combination of sales experience and Scientific knowledge, Ron is responsible for everything related to the Pharmaceutical portfolio offered by Heuft USA.
Ron Received his Bachelor’s Degree in Chemistry from Western Illinois University in 2008.
 


General Manager
HEUFT USA Inc
Pharmaceutical Sales Engineer
HEUFT USA Inc

START TIME 10AM CDT / 4PM BST DURATION 45 MINS

START TIME 10AM CDT / 4PM BST DURATION 45 MINS
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START TIME 10AM CDT / 4PM BST DURATION 45 MINS

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WHAT IS CPD?

CPD stands for Continuing Professional Development’. It is essentially a philosophy, which maintains that in order to be effective, learning should be organised and structured. The most common definition is:

‘A commitment to structured skills and knowledge enhancement for Personal or Professional competence’

CPD is a common requirement of individual membership with professional bodies and Institutes. Increasingly, employers also expect their staff to undertake regular CPD activities.

Undertaken over a period of time, CPD ensures that educational qualifications do not become obsolete, and allows for best practice and professional standards to be upheld.

CPD can be undertaken through a variety of learning activities including instructor led training courses, seminars and conferences, e:learning modules or structured reading.

CPD AND PROFESSIONAL INSTITUTES

There are approximately 470 institutes in the UK across all industry sectors, with a collective membership of circa 4 million professionals, and they all expect their members to undertake CPD.

For some institutes undertaking CPD is mandatory e.g. accountancy and law, and linked to a licence to practice, for others it’s obligatory. By ensuring that their members undertake CPD, the professional bodies seek to ensure that professional standards, legislative awareness and ethical practices are maintained.

CPD Schemes often run over the period of a year and the institutes generally provide online tools for their members to record and reflect on their CPD activities.

TYPICAL CPD SCHEMES AND RECORDING OF CPD (CPD points and hours)

Professional bodies and Institutes CPD schemes are either structured as ‘Input’ or ‘Output’ based.

‘Input’ based schemes list a precise number of CPD hours that individuals must achieve within a given time period. These schemes can also use different ‘currencies’ such as points, merits, units or credits, where an individual must accumulate the number required. These currencies are usually based on time i.e. 1 CPD point = 1 hour of learning.

‘Output’ based schemes are learner centred. They require individuals to set learning goals that align to professional competencies, or personal development objectives. These schemes also list different ways to achieve the learning goals e.g. training courses, seminars or e:learning, which enables an individual to complete their CPD through their preferred mode of learning.

The majority of Input and Output based schemes actively encourage individuals to seek appropriate CPD activities independently.

As a formal provider of CPD certified activities, SAE Media Group can provide an indication of the learning benefit gained and the typical completion. However, it is ultimately the responsibility of the delegate to evaluate their learning, and record it correctly in line with their professional body’s or employers requirements.

GLOBAL CPD

Increasingly, international and emerging markets are ‘professionalising’ their workforces and looking to the UK to benchmark educational standards. The undertaking of CPD is now increasingly expected of any individual employed within today’s global marketplace.

CPD Certificates

We can provide a certificate for all our accredited events. To request a CPD certificate for a conference , workshop, master classes you have attended please email events@saemediagroup.com

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