WEBINAR: Marketing Medical Devices:
Are your promotional materials compliant?

On Thursday 19th October 2023, JensonR+ Regulatory Manager (Medical Devices) Tom Wood, hosted a webinar that highlighted the importance of ensuring your medical devices promotional materials are compliant with industry codes and adhere to legal guidelines.

This webinar was brought to you in partnership with Medilink Midlands,

In the webinar, Tom provides guidance on the common pitfalls associated with marketing medical devices, offering advice on how these can be avoided within your own promotional materials.

From websites, conference collateral, digital/printed ads, audio-visual material through to prescribing information; promotional copy requires a technical review in order to prevent violations of industry codes and to ensure that legal guidelines are followed.

Tom Wood
JensonR+ Regulatory Manager
(Medical Devices)

Please see below for several resources that Tom referred to in his presentation:

  • For further details relating to the support that JensonR+ can offer, please click here.
  • For more information on NEXTEC Medical, please click here.
  • If you’d like to book a one-to-one meeting with Tom, please click here.

Our expert team work with you to make the promotion and launch of your product a success. They provide both medical and regulatory review and certification services for promotional copy through our team of registered copy approvers. We can review your promotional literature, advise you on campaign strategy and key messages, and obtain regulatory approval through pre-vetting where necessary.

Our UK team of Medical Devices / IVD experts are here to support and guide you through the complex and ever-changing regulatory landscape. With many years of experience in the industry and with notified/UK-approved bodies we offer comprehensive regulatory services to suit your business.

Our track record of working with the MHRA, various competent authorities and multiple notified/UK-approved bodies ensure we can offer you the most efficient regulatory support.

We have years of experience working with the medical device directive 93/42/EC, The In Vitro Diagnostic Directive (98/79/EC) regulation, and now the UK MDR 2002 and regulations 2017/745 and 2017/746  on Medical Devices and in vitro diagnostics in the EU.

Not only can JensonR+ support you in navigating regulatory compliance we can also support you in creating and maintaining a compliant quality management system to meet the requirements of regulations, ISO 13485, MDSAP and GxP.

The JensonR+ team is supported by an extensive regulatory network in over 90 countries; this allows us to be the one-stop shop for all things regulatory both in the UK and beyond.