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.
Medilink Midlands Patrons, JensonR+ 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. JensonR+ can review your promotional literature, advise you on campaign strategy and key messages, and obtain regulatory approval through pre-vetting where necessary.
Following our pharmaceuticals-focused webinar back in April, this session will be delivered by Tom Wood, Regulatory Manager of Medical Devices at JensonR+. Tom will be providing guidance on the common pitfalls associated with marketing medical devices, offering advice on how these can be avoided within your own promotional materials.
Tom highlights why this is such an integral aspect of your innovation’s success:
“In addition to verifying that your promotional material and labelling is compliant with the relevant legislation, copy approval of your promotional material can mean maintaining your company’s strong reputation. By ensuring all your materials are accurate, balanced, fair, substantiated, up-to-date, and compliant with the codes of practice you can be secure that your materials are the best they can be.”
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Speaker Profile
Tom Wood, Regulatory Manager – Medical Devices, JensonR+
Tom joined JensonR+ in May 2023 as Regulatory Manager – Medical Devices. He has experience in industry and notified bodies as an auditor and technical expert and has worked in both CE and UKCA marketing alongside ISO 13485, ISO 9001 and MDSAP.
Tom now manages a portfolio of medical clients at JensonR+ offering consultancy and market access services to a variety of companies from start-ups to multi nationals.