Faster compliance reviews. Lower operating cost.
AI for SDS, labeling, and regulatory work in chemical and pharma teams - with specialists keeping the final call.
SDS intake, diffs, and release queues
Cited answers over controlled regulatory text
Consulting playbooks turned into repeatable AI steps
Pilot program
Join the pilot
Ship one high-volume workflow first - SDS triage, questionnaires, or change control - then expand.
Mission
Lower compliance cost. Keep regulatory confidence.
For chemical manufacturers, pharma SMEs, and RA consultancies drowning in document volume.
Automate the repetitive
Cut the hours spent on SDS diffs, questionnaire packs, and status chasing so specialists spend time on judgment calls.
Catch risk earlier
Surface missing languages, drifted classifications, and open findings before they delay a release or an audit.
Keep decisions owned
AI drafts and ranks; named reviewers approve, reject, or escalate with a trail you can show an inspector.
Platform
Workflows for SDS, labels, and regulatory change
Guided AI steps for high-volume compliance work. Experts stay responsible for release.
SDS & regulatory review
Intake, version diffs, completeness checks, and release queues in one workspace - not across inboxes and shared drives.
Document
Output
Workflow brief synced
Cited compliance answers
Ask in plain language over controlled SDS and regulatory text. Answers come with sources your reviewers can verify.
Visibility retained · final action gated
Experts stay in control
Automation clears volume. Qualified people keep disposition. Lower cost without unsupervised publication.
Product
See Obsevia chat
Two-minute walkthrough, then sign up for the public product.
Try Obsevia chat
Public signup for conversational compliance support on controlled document context. No private customer environment required.
Services
Compliance, consulting, and custom software
Operate regulated work with AI, bring specialists when you need judgment, or modernize, integrate, and build the systems your team relies on.
Team
Who you work with
Engineering, go-to-market, and sales focused on regulated chemical and pharma buyers.
Julian Kleber
Cofounder & AI Engineering
Owns the AI and platform layer behind Obsevia's compliance workflows.
Kaja Szumilo
Cofounder & Marketing
Owns brand, messaging, and go-to-market for regulated buyers.
Rohan Pathak
Growth Manager
Runs outbound and pilot conversations with chemical and pharma teams.
Free resources
Research report and one-pager
Confirm your work email to download both PDFs for EU compliance automation.
FAQ
Common questions
Short answers about what Obsevia builds and how humans stay in control.
What does Obsevia do?
Obsevia builds AI workflows for SDS, labeling, and regulatory reviews, and also delivers compliance management, consulting, software modernization, software integration, custom apps, AI development, sovereign AI, and research services focused on simulations and AI for chemical and pharma teams.
Who is Obsevia for?
Mid-market chemical, pharma, and medtech teams that need faster compliance reviews, lower operating cost, and custom software or AI features with human oversight.
Does Obsevia replace regulatory specialists?
No. AI drafts and ranks work; named reviewers approve, reject, or escalate. Consulting and custom development support specialists rather than replace them.
What services does Obsevia offer?
Compliance management, regulatory consulting, software modernization, software integration, custom software development, AI development, sovereign AI, and research services (simulations and AI).
Contact
Talk to Obsevia
Pilots, consulting, or product questions - send a short note and we route it.
Response
Use the form for the fastest routing to the right person.