For products that do not explain themselves: complex to grasp, high-priced, tightly regulated, with no standard playbook. I build the evidence your buyers need to win internally.
Schedule a ConsultationSound familiar?
Four problems every regulated healthcare company knows.
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My answer
Drafts arrive with sources and references attached. That saves the rounds spent chasing evidence.
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One person. Strategy, content, Medical Affairs. All of it.
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Material that cites studies correctly and names its limits does not bounce off. 4 years MSL.
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Every text comes with a note on the rule it rests on. You are the one who signs it off.
Services
Consulting, campaign, standard building block, stage. Four routes, one contact.
The filter between idea and publication: material is built to clear review from the start instead of looping through expensive corrections. Plus an external Medical Affairs department on call, pharma standards without full-time headcount. Risk navigation, not legal advice, final sign-off stays with the client. Before every campaign I check the client, the indication and the evidence base.
Complete marketing campaigns, creatively designed with regulatory awareness built in from day one. Material goes into approval instead of a third round of corrections.
Standardised building blocks, developed once and deployed repeatedly: scalable, regulatory-reviewed, ready to use.
Keynotes, panel discussions, and hosting at congresses, corporate events, and media formats: scientifically grounded, clearly communicated, delivered with stage presence.
Approach
I work on products that come without a template. No model claim, no reference case, no safe route.
How I work
What I do not do
Nominated among the top four submissions in the Medical Education category, at Germany's first award for excellence in healthcare communications.
Medical Education category, for outstanding achievements in medical professional communication, evaluated on strategic relevance and implementation quality.
Platform
Curated studies and evidence reports on cannabis medicine. Free. No ads. No tracking. Just science.
I built mechoulam.de in the evenings and at weekends, with no client and no funding. Anyone looking something up on cannabis in medicine otherwise pulls the studies from several databases and then has to judge alone which ones hold up. On mechoulam.de they sit in one place, sorted by study type, strength of evidence and indication.
About me
Diplom-Biologist · Medical Science Liaison · HWG and Regulatory
I am Bertan Türemis, a qualified biologist from the University of Kassel, with 8 years of life sciences experience, including 4 years as a Medical Science Liaison in Germany's cannabis industry. My focus lies at the intersection of science, regulation, and communication.
bemedica consult fills a clear market gap: bringing a product to market under tight regulatory constraints takes Medical Affairs at pharma level with genuine industry expertise. I factor in regulatory thinking from the very first idea. That is how concepts emerge that noticeably shorten the approval process.
Career Stations
Ranked by Favikon as the leading cannabis content creator on LinkedIn, worldwide. Reach here is proof that professionals read what I write, not advertising space.
Frequently asked
Contact
Write a few lines about your case. I will get back to you.
