Summary
What is defined as advertising when engaging HCPs? Where and when is communication with HCPs at risk of being non-compliant advertising for a soon-to-be-launched Rx medicinal product? How do you work in a compliant way with influencers/3rd parties? In short: what is legal and compliant?
All these considerations are important when preparing your pre- and post-launch work.
Regardless of whether you’re working in Medical Affairs, Market Access, Commercial, or another part of a pharma company, all the organisation’s activities and dialogues with HCPs, patients, and payers must comply with
• Danish law and industry ethical codes on advertising for prescription medicinal products
• HCPs’ association with pharma companies
• GDPR rules.
Are your activities legal and compliant?
Join this one day course for a compliance check of your activities and dialogues with HCPs, patients, and patients’ associations – before and after launch.
But it's not just about barriers: despite the many rules, there are ample opportunities to think creatively in your campaigns.
We work with real-life cases to make learnings directly applicable in your daily tasks.
Other course participants say
"The course was remarkably relevant. Very skilled and inspiring presenters - high level of knowledge!"
Vibeke Søndergaard, Compliance Manager, Effector A/S
"If you work with pre-launch products this course gives you a detailed overview of the rules and what to pay attention to."
Jesper Kildehøj, Senior Medical Advisor, Daiichi Sankyo Nordics
Keywords
- Rx Pre-launch and Post launch
- Marketing compliance
- GDPR rules
- HCP interaction
- Disease and treatment awareness
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Course leader & lecturers
- Louise Bertelsen FormanCourse leaderPartner, Attorney-at-law
Loeven Advokatfirma - Elisabeth Gammelgaard LudvigCourse leaderOwner
Sundhedsagenda
Is this course for you?
The course is for you who communicate with HCPs and/or patients as part of your responsibilities. You might work as a Medical Affairs Manager, Medical Scientific Liason (MSL), Key Account Manager, Commercial Manager, Market Access Manager, or Patient Engagement Manager.
What you will learn
- Through cases you get a handle on how to collaborate and communicate within legal and ethical guidelines with important external stakeholders such as HCPs, patients’ associations, and patients before and after the launch of a prescription medicinal product.
- The effect of GDPR and association rules for working with HCPs, such as KOL (Key Opinion Leader) mapping, advisory boards, Investigator Initiated Trials (IITs), market research, conference work, and continued education.
- GDPR legislation and ENLI's code for collaboration with individual patients and patients’ associations on disease awareness, clinical research, pipeline, patient advocacy, and use of SoMe in connection with launches.
What your company will get
- An employee who can collaborate with HCPs, patients’ associations, and patients in a compliant manner.
- An employee who can communicate effectively within GDPR legislation as well as the agreed association and ethical rules for the industry.
- An employee who knows the do's and don'ts of working with external stakeholders before and after the launch of a prescription medicinal product.
Course calendar
- Compliance before and after launch in collaboration and dialogue with HCPs.
- Practical example: this is how a pharma company works with compliance in their dialogue and collaboration with HCPs.
- GDPR challenges in collaboration with HCPs and patients.
- Case work on collaborative projects with patients’ associations and individual patients, e.g.:
- Focus groups
- Market research
- Events
- Lectures
- Information material
- Patient cases
- Influencer collaboration
- Own or 3rd party SoMe efforts
- "Fair market value" for remuneration of patients
Registration
Registration deadline13 May 2024
Lersø Parkallé 101
2100 København Ø
Course information
Literature
Prior to the course you get access to mandatory and/or optional readings via your personal Atrium log-in.
Prerequisites
If you are not familiar with the Danish marketing compliance rules and guidelines, we strongly encourage you to purchase and complete “E-learning: The Danish pharmaceutical Industry’s Promotional Code” BEFORE attending the course. The e-learning provides you with basic knowledge about the key rules and standards regulating communication and interactions with HCPs, patients, and decision-makers regarding pharmaceutical products in a Danish context.
Examination
There is no examination for this course.
This course is an elective course for the Diploma in Marketing Compliance.
This course is a part of a diploma
Through the Diploma in Marketing Compliance, you will get an in-depth understanding of the rules and regulations set by both the authorities and the pharmaceutical industry in Denmark and Europe, making you sharper and more effective in your daily work
Read moreCourse leaders
Loeven Advokatfirma
Sundhedsagenda
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Want to know more or need help?
Contact Client Manager Ida Salicath at +45 39 15 09 46
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