COGNEX FUTURE PHARMACEUTICAL TECHNOLOGY

WE INVITE YOU TO SPEND ONE DAY IN THE FUTURE

TRACEABILITY AND QUALITY ASSURANCE

We are pleased to invite you to an exciting event about traceability and quality assurance in the pharma and healthcare sector. The event will take place on november 14th. at 9AM at Birkedam 10L, 6000 Kolding.

Traceability and quality assurance are important topics in many industries, especially in the pharmaceutical and health sectors. Traceability and quality assurance are essentials for creating trust and credibility in the pharma industry, as well as for protecting consumers and pattens from errors and risks. By having clear guidelines and standards for traceability and quality assurance, the pfarma industry can contribute to improving public health and innovation. By using UID you can mark your products, processes and services with a unique code that allows you to track them throughout the value chain. 

UID – BENEFITS

UID stands for Unique Device Indentification, which is a system that aims to provide a single, globally harmonized way of identifying medical devices through their labls, packages, and sometimes directly on the device itself. One of the benefits of UID is that it can help track and trace medical devices throughout thier lifecycle, from manufacturing to distribution to patient use. This can improve the quality and efficiency of recalls, adverse reporting, and inventory management.  UID is also enable to give better access to device information, such as chilical data, performance data, or safety data. Which means it can help you improve the quality, efficiency and patient safety of your business.

LEADING EXPERTS FROM COGNEX

We will have top leading experts from COGNEX as Joshua Deats  and Jesper Jørgensen at the event to share their knowledge and experiences with you.  Joshua Deats is the Global packaging Manager in the Pharma & Medical device manufacturing and Jesper Jørgensen is the Sales Leader of Factory Automation in the North Europe. You will have the opportunity to network with other professionals and experts who shares your interest in these topics. In addition, you will get insight into what the future brings and how you can prepare for the upcoming challenges and opportunities. 

KEY CONSIDERATIONS

CFR stands for the Code of Federal Regulations, and 21 CFR Part 11 deals primarily with the movement of paper-based records to electronic records with the goal of maintaining resiliency in the pharmaceutical supply chain. Serialization and track-and-trace programs provide visibility at every point along the supply chain and allow for a more rapid response to supply problems. Pharma manufacturers want to install vision systems on their lines to help with automation but also want to stay compliant. Fortunately, automation and compliance work well together. Building 21 CFR Part 11 compliance from the start guarantees that serialization, track-and-trace, defect detection, and other processes can be fully automated while maintaining compliance.

REGISTRATION

The event is free, but registration is required. The number of seats are limited, so hurry up and secure your place.

Participation in the event is binding, which means that a no-show fee has been arranged. The fee is DKK 750 ex. VAT. A cancellation must be sent before the Nov. 3TH 2023.

You are also required to sign an NDA as we are talking about business opportunities that we are not offering to the world yet.

Sign right here.

We look forward to seeing you at the event and sharing our knowledge and experience with you. Her is a link to the agenda for the day.

PHARMA EVENT – AGENDA

Sincerely,

COGNEX