The countdown to EU FMD compliance is underway. Join us and be prepared.
Getting ready for Falsified Medicines Directive (FMD) compliance can be a complex process. Avoid supply interruption. Make sure you have a robust, realistic plan to meet the February 9, 2019 EU FMD compliance deadline.
Less than two years remain ─ will you be ready in time? With 32 countries across Europe being affected by this serialisation legislation, the entire industry must prepare. This webinar will help ensure you have a solid, comprehensive strategy and implementation plan in place before it is too late.
Without an effective plan, you risk facing significant product supply issues once the deadline is enforced. Join Be4ward, OPTEL and Verify Brand for this informative webinar –
Learn how to:
- Develop an effective strategy for EU FMD compliance with low risk to your business
- Implement your EU FMD plan with minimal impact to your resources
- Identify key solutions, specially designed for rapid implementation
To find out more about the webinar, click here.
November 14, 2017 1PM GMTRegister Now!
Be4ward is a niche consultancy company helping Pharmaceutical, Biotech and Medical Devices companies and their supply base improve their serialisation, labelling and artwork capabilities. Be4ward help clients define the most efficient business processes, organization design and, being completely independent, help them select and implement the most appropriate service providers and IT systems to meet their needs. Be4ward helps these companies improve patient safety and drive additional value from their product range. Corporate website: www.be4ward.com Contact: email@example.com
Should you have any questions about this or any other of my blogs, or would simply like to request a copy of my booklets, please don’t hesitate to contact me at Stephen.McIndoe@be4ward.com.
For more information on serialisation, go to our free download section.