VERTANICAL is hiring medical affairs, scientific marketing and a field team for the launch, and doctors who hear about the medicine from a representative or at a congress will check the company website. The German homepage, last updated in August 2025, still names the application for approval as the milestone, and the English homepage says the application was submitted. Neither mentions that approval came in June 2026, although the press page and every job post do.
First action
Draft the new milestone paragraph in German and English and send it to Regulatory.
How to measure it
Homepage-to-portal click rate
- Now
- –
- Target
- +50%
- By
- 60 days
Steps
Draft text
Corporate status in German and English, no product claims.
Communications (PR) 1 day
Regulatory and legal review
Every text checked against the rules for medicines information in Germany and Austria.
Team Lead/Director Regulatory Affairs 1 week
Update homepage
Milestone paragraph and pipeline status.
Website manager 1 day
Add HCP entry
A "Für Fachkreise" button near the top.
Website manager 1 day
Align English
Same status on /en/.
Website manager 1 day
Brief the field team
What the public site says now.
Medical field team lead 1 day
Measure
Clicks from homepage to the portal and DocCheck logins.
(Senior) Manager Scientific Marketing/Medical Affairs monthly
Why it works
Update the corporate milestone text in both languages to the factual status (approved in Germany and Austria, launch under way, US studies continuing), in wording Regulatory approves. Keep the brand name and all product information inside the DocCheck portal, and add a clear "For healthcare professionals" entry point near the top of the homepage.
The public site then matches what doctors hear from the field team, and they reach the portal in one click without the company promoting a prescription medicine to the public.
Ready to use
ChecklistHomepage update list
[ ] German milestone sentence updated (approval, not application) [ ] English milestone sentence updated [ ] Pipeline status matches the approval [ ] No product claims or brand promotion on public pages [ ] "Für Fachkreise" entry point above the fold [ ] Regulatory and legal sign-off recorded [ ] Field team briefed
Risks and how to handle them
Wording could read as promotion
Regulatory signs off; product information stays behind the login.
Status differs by country
State approval only for Germany and Austria.
Evidence
- Your websiteGerman homepage (sitemap last modified August 30, 2025): "Mit dem Antrag auf Zulassung von VER-01 als Fertigarzneimittel zur Behandlung chronischer Kreuzschmerzen haben wir einen bedeutenden Meilenstein erreicht" (the application, not the approval); it does not mention the approval or the name Exilby. The pipeline lists six chronic low back pain studies, including ELEVATE against opioids, with osteoarthritis and diabetic neuropathy studies "Geplant".Source
- Your websiteEnglish homepage: "With the submission of our marketing application for the approval of VER-01 in Germany we have reached an important milestone"; no English area for healthcare professionals: its "Fachkreise" link leads to the German-language portal.Source
- Your websitePress page: "Mit der Zulassung unseres ersten Fertigarzneimittels haben wir ... einen wichtigen Meilenstein" reached; lists "VERTANICAL erhält Zulassung" (June 9, 2026), the FDA Breakthrough Therapy designation (May 18, 2026), the German Pain and Palliative Care Days in Frankfurt 2026 and coverage in Bloomberg, Forbes, Business Insider, WELT, BILD and ntv. Each release opens in a pop-up from a "#" link; the approval release's own page is set to noindex, nofollow and nosnippet and is not in the sitemap.Source
- HiringEvery VERTANICAL post says VER-01, a cannabinoid-based medicine for chronic pain, "was approved in June 2026 under the name Exilby in Germany and Austria"; "approval in the USA is planned for 2029", and the goal is to establish Exilby as a leading chronic pain therapy by 2030 (translated). Applications go to FUTRUE GmbH in Gräfelfing.Source
- Hiring(Senior) Manager Scientific Marketing/Medical Affairs (Gräfelfing, posted September 23, 2026; German post, translated): develops "medical-scientific communication concepts and materials for communication with doctors and pharmacists", analyses competitors' marketing, plans events and congresses "initially focused on Germany but increasingly with an international component", builds formats for KOLs, prepares study results for the trade press, and answers "medical enquiries from doctors and pharmacists" with quality-assured responses agreed with Regulatory and Clinical Trials.Source