EVENTS

PRISYMID will be showcasing FDA compliant labeling systems and clinical trial label control management solutions and services at the following life science events.

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West Coast Clinical Supplies Forum

6th-7th October 2009
Hilton San Diego Mission Valley, San Diego, CA
Website: Click Here

Presentation :Automate Clinical Trial Labelling in Compliance with FDA21 CFR Part 11

Evaluate techniques used to improve data integrity and manage vital information on labels for randomized trials. Find out how clinical trials projects spanning borders and continents can take advantage of web based technology to manage labeling control. This presentation is an opportunity to evaluate your current systems and see how they measure up to FDA standards, industry best practice and whether new technology could offer any significant advantages and benefits.

  • Improve data integrity
  • Increase efficiency 
  •  Discover compliance pitfalls and learn how to avoid them
Bob Brunk, Life Sciences Manager, PRISYMID
 
For more information contact us at : info at prisymid dot com
 

Labelling and Packaging Compliance for Medical Devices

27th-28th October 2009
Hilton London Olympia, London, UK
Website: Click Here

Presentation :The Use of Labelling Systems in Meeting FDA Requirements for UDI

  • The role that smart design and labelling systems can play in meeting these requirements
  • How these systems can also help in meeting 21 CFR Part 11 for security and electronic signatures
  • How these systems can help organisations looking to collaborate online with external supply chain partners where packaging and labelling may be performed by a third party
Dave Taylor, Life Sciences Product Manager, PRISYMID
 
For more information contact us at : info at prisymid dot com
 

Pharmaceutical Labelling & Packaging Summit

27th-28th October 2009
Hilton London Olympia, London, UK
Website: Click Here

Presentation : Insight into Upcoming Specific Country RequirementsResponding to industry trends and legislation affecting label management 

Insight into Upcoming Specific Country Requirements 
  • Exploring the future developments for labelling and packaging in Turkey, Serbia, France, etc. 
  • Use of unique identity codes, comprised of GTIN, batch number and expiry date to authenticate medicines globally 
  • Novel mechanisms to empower manufacturers to make use of existing product lines and maintain compliance with the imminent regulations  
Dave Taylor, Life Sciences Product Manager, PRISYMID
 
For more information contact us at : info at prisymid dot com
 

VIBs 5th Annual Pharma Labelling & Packaging Conference

29th September - 1st October 2009
Hotel Vier Jahreszeiten Kempinski, Munich, Germany
Website: Click Here

Presentation : Responding to industry trends and legislation affecting label management

Responding to industry trends and legislation affecting label management 
  •  Managing the changing demands on label space and legally required label information 
  •  Meeting the challenges of global label management across disparate locations 
  •  Taking advantage of new technologies to improve label production accuracy and efficiency 
 Dave Taylor, Life Sciences Product Manager, PRISYMID
 

MedTech Ireland

23rd-24th September 2009
Radisson SAS Hotel, Galway, Ireland
Website: Click Here

PrisymID Joins MedTech Ireland

 

PRISYMID is pleased to be exhibiting at MEDTEC IRELAND, the only event dedicated to industry professionals engaged in the design and manufacturing of medical devices in the country. 

In recent years Ireland has become one of the world’s most important development and manufacturing hubs for medical devices. With 8 out of 10 of the world’s largest medical manufacturers actively manufacturing in the country, analysts estimate the value of medical devices manufactured in Ireland at around €5 Billion.

For more information contact Prisym Marketing at:info at prisymid dot com and visit the conference website at: www.medtecireland.com

 

CBI's 4th Clinical Supply Chain Management Conference

30th - 31st July, 2009
Princeton, New Jersey
Website: Click Here

PRISYM ID's life sciences products manager, Dave Taylor will be giving a candid, case study based presentation on implementing a compliant clinical trials labeling management system to achieve greater data integrity and increased efficiency. Also included in the presentation is a look at the advantages web based technology offers clinical trials labeling control.

For more information or to register for this conference please visit the website linked above.

 

European Life Sciences Forum 2009

31st March - 1st April
Sofitel London Heathrow, London
Website: Click Here

Life Sciences Forum 2009

Prisym ID will be exhibiting at the Life Sciences Forum 2009.

This informative conference will deliver content critical to all areas of the life sciences industry, including discussion on important topics and issues facing clinical development, sales and marketing, manufacturing, and the end-to-end supply chain. We will also be looking at ways for the industry to use technology to drive innovation across all parts of the business. You will hear how Oracle solutions have enabled organizations in this industry to shorten their time to market, gain operational efficiencies, enforce regulatory compliance, reduce costs, improve customer loyalty, and grow revenues.

For more information, click on the banner to be taken to the Life Sciences Forum website.

 

Pharmaceutical Labelling & Packaging Conference

February 18-19th 2009
Hyatt Regency Hotel, Penns Landing, Philadelphia
Website: Click Here

PRISYM ID will be presenting on the Impact of Industry Trends and Legislation on Labelling. Technical solutions to common issues will be included.

 

7th Annual Change Control Conference

January 26-28th 2009
Marriott Courtyard Hotel, Philadelphia, USA
Website: Click Here

PRISYM ID will be presenting on managing and controlling changes to label formats within an FDA regulated environment.

To qualify for a special discounted rate for this conference email your contact details and the event you are interested in to

FDA 21 CFR Part 11 Compliance