White Plains Youth Bureau’s After School Connection ProgramMadhu Kumar
A graduate of the Massachusetts Institute of Technology, Madhu Kumar most recently served as a scientific advisor for Wilson Sonsini Goodrich & Rosati, where he drafted and prosecuted patent applications in the pharmaceutical and life sciences industries. Madhu Kumar has also tutored children and youths through the White Plains Youth Bureau.
Medical Device Tracking Symposium SeriesDaren Mooney
A comprehensive educational program by way of webinar-based and interactive sessions providing important background, education and expert-moderated panel discussions of topics relevant to UDI compliance, best-practice and future trends.
The £100bn customer; doing business with the NHSENGAGE_Events
Do you want to engage with one of the UK’s biggest organisations? Not sure where to start? These slides are from our free event in partnership with Wessex Academic Health Science Network that delved into the intricacies of working with the NHS. To find more events like this, visit www.science-park.co.uk/events
White Plains Youth Bureau’s After School Connection ProgramMadhu Kumar
A graduate of the Massachusetts Institute of Technology, Madhu Kumar most recently served as a scientific advisor for Wilson Sonsini Goodrich & Rosati, where he drafted and prosecuted patent applications in the pharmaceutical and life sciences industries. Madhu Kumar has also tutored children and youths through the White Plains Youth Bureau.
Medical Device Tracking Symposium SeriesDaren Mooney
A comprehensive educational program by way of webinar-based and interactive sessions providing important background, education and expert-moderated panel discussions of topics relevant to UDI compliance, best-practice and future trends.
The £100bn customer; doing business with the NHSENGAGE_Events
Do you want to engage with one of the UK’s biggest organisations? Not sure where to start? These slides are from our free event in partnership with Wessex Academic Health Science Network that delved into the intricacies of working with the NHS. To find more events like this, visit www.science-park.co.uk/events
Leveraging UDI Database Requirements to Drive Data GovernancePTC
Delivered at the event “UDIs and Traceability for Medical Devices 2014” in Munich, May 21 – 22, 2014, Europe's only UDI-dedicated event for the medical device industry – with keynotes from the FDA and European Commission– this slideshare presents a Solution Provider’s perspective on the impact of Master Data on the UDI submission to the FDA UDI data base. In detail, the presentation highlights the following subjects:
- A checklist for compliance – What to consider when selecting a solution for UDI data submission
- Data management as a lever for streamlined submissions – Current situation, challenges, and best practices for establishing data governance within an organization
- How PTC solutions support UDI and data governance – PTC’s UDI solution and the broader approach for central product data management
Quality Manufacturing in Healthcare ASQ 2015Gerard Pearce
This presentation highlights some of the major challenges that companies in the healthcare industry face in establishing and enforcing quality and other important controls and practices. The presentation explores some of the primary issues and concerns in the industry, and highlights some of the trends being seen across a variety of production environments. In response to these issues new methods and tools are presented, along with lessons learned from other industries.
Key Concerns in the Pharmaceutical and Healthcare Supply Chain - D.Quinn Apri...Dan Quinn
This is the output of a recent Achilles sponsored round-table on Supply Chain Risk Management at the ProcureCon Health 2013 event in Zurich - hope you find it interesting. Regards, Dan.
Leading stockist and supplier of a range of healthcare gadgets, asthma care equipment, slimming equipment, BP care equipment, diabetes equipment, Portable Oxygen, Vaporizer Machine, Asthma Care Equipment.
Innovatie in de zorg - Van Dr. Google Naar Dr. WatsonRobin Hooijer
Gepresenteerd bij de algemene ledenvergadering van NVKFM (Nederlandse Vereniging voor Klinisch Fysisch Medewerkers in het Radboudumc te Nijmegen. 8 juni 2016.
How to Make Postmarket Surveillance More Cost EffectiveApril Bright
When it comes to postmarket surveillance (PMS), it’s common for the costs to outweigh the value. But, by working with the right team, you’ll be able to execute a study that maximizes return on investment and minimizes the financial impact of conducting further observational research. Postmarket study challenges that must be addressed include enrollment delays, patient attrition, long-term follow-up, resourcing demands and global payor requirements. This session will provide a case study of one orthopaedic company’s seamless transition between postmarket approval and post-approval studies.
As UDI deadlines roll out, OEMs are left with many questions on implementation and compliance, including:
How does FDA recommend we direct mark screws and small implants?
How should we proceed as we await the guidance on the Convenience Kit exemption?
What are best practices for entering submissions to GUDID?
How is FDA enforcing UDI?
FDA officials will speak on UDI adoption and UDI data quality. Bring your questions. Ample time will be saved for Q&A.
- HealthTech innovation is disrupting healthcare and its established players
- Technology is driving a new paradigm to create better health care
- Developing markets can leapfrog their healthcare infrastructure limitations
- New opportunities are opening to shape the new paradigm
Leveraging UDI Database Requirements to Drive Data GovernancePTC
Delivered at the event “UDIs and Traceability for Medical Devices 2014” in Munich, May 21 – 22, 2014, Europe's only UDI-dedicated event for the medical device industry – with keynotes from the FDA and European Commission– this slideshare presents a Solution Provider’s perspective on the impact of Master Data on the UDI submission to the FDA UDI data base. In detail, the presentation highlights the following subjects:
- A checklist for compliance – What to consider when selecting a solution for UDI data submission
- Data management as a lever for streamlined submissions – Current situation, challenges, and best practices for establishing data governance within an organization
- How PTC solutions support UDI and data governance – PTC’s UDI solution and the broader approach for central product data management
Quality Manufacturing in Healthcare ASQ 2015Gerard Pearce
This presentation highlights some of the major challenges that companies in the healthcare industry face in establishing and enforcing quality and other important controls and practices. The presentation explores some of the primary issues and concerns in the industry, and highlights some of the trends being seen across a variety of production environments. In response to these issues new methods and tools are presented, along with lessons learned from other industries.
Key Concerns in the Pharmaceutical and Healthcare Supply Chain - D.Quinn Apri...Dan Quinn
This is the output of a recent Achilles sponsored round-table on Supply Chain Risk Management at the ProcureCon Health 2013 event in Zurich - hope you find it interesting. Regards, Dan.
Leading stockist and supplier of a range of healthcare gadgets, asthma care equipment, slimming equipment, BP care equipment, diabetes equipment, Portable Oxygen, Vaporizer Machine, Asthma Care Equipment.
Innovatie in de zorg - Van Dr. Google Naar Dr. WatsonRobin Hooijer
Gepresenteerd bij de algemene ledenvergadering van NVKFM (Nederlandse Vereniging voor Klinisch Fysisch Medewerkers in het Radboudumc te Nijmegen. 8 juni 2016.
How to Make Postmarket Surveillance More Cost EffectiveApril Bright
When it comes to postmarket surveillance (PMS), it’s common for the costs to outweigh the value. But, by working with the right team, you’ll be able to execute a study that maximizes return on investment and minimizes the financial impact of conducting further observational research. Postmarket study challenges that must be addressed include enrollment delays, patient attrition, long-term follow-up, resourcing demands and global payor requirements. This session will provide a case study of one orthopaedic company’s seamless transition between postmarket approval and post-approval studies.
As UDI deadlines roll out, OEMs are left with many questions on implementation and compliance, including:
How does FDA recommend we direct mark screws and small implants?
How should we proceed as we await the guidance on the Convenience Kit exemption?
What are best practices for entering submissions to GUDID?
How is FDA enforcing UDI?
FDA officials will speak on UDI adoption and UDI data quality. Bring your questions. Ample time will be saved for Q&A.
- HealthTech innovation is disrupting healthcare and its established players
- Technology is driving a new paradigm to create better health care
- Developing markets can leapfrog their healthcare infrastructure limitations
- New opportunities are opening to shape the new paradigm
Digitale pathologie (de digitalisering van de pathologie) heeft zich in hoog tempo ontwikkeld. Een aantal Nederlandse pathologielaboratoria beschikken over een of meerdere coupescanners en een groot deel van de laboratoria overweegt de aanschaf ervan. De digitale beelden, Whole Slide Images (WSI), worden in eerste instantie vooral kleinschalig gebruikt voor expertpanels, collegiale consultaties en revisies. Straks zal echter het grootste deel van de primaire diagnostiek op basis van WSI worden bedreven. Welke kansen biedt deze doorontwikkeling van de digitale pathologie? Hoe kan Nederland deze kansen optimaal benutten? Dat zijn de vragen die we met deze whitepaper willen beantwoorden.
4K HD in Hoger Onderwijs en Onderzoek: een overviewSylvia Moes
Presentatie over 4K HD in Hoger Onderwijs. Uiteenzetting van wat 4K HD is, hoe het nu vooral toegepast wordt, en wat de kansen zijn in het HO, waarin ook aandacht voor implementatie is.
Presentatie over GS1 Nederland. Aandachtsgebieden:een passend aanbod voor de consument, efficiente vernieuwende en duurzame logistiek en het delen van informatie in de keten.