SPL
Structured Product Labeling for USPI, PPI, IFU, and Medication Guides.
Send us your approved labels in Word or PDF. We convert them to structured, validated, submission-ready outputs: SPL, SPM, EMA & Jordan FHIR, and PharmaLedger ePI, with quality control and turnaround in days.



Every conversion type
As global markets adopt structured and electronic labeling, the formats multiply. We convert to all of them, and we keep up as new ones arrive.
Structured Product Labeling for USPI, PPI, IFU, and Medication Guides.
Structured Product Monograph for the Canadian market.
Electronic Product Information on the HL7 FHIR standard for the EU.
ePI on FHIR for the Jordan FDA's current structured requirement.
The PharmaLedger ePI standard, used globally where FHIR isn't adopted.
Exclusive conversion partner to the PharmaLedger Association.
How it works
Upload approved MS Word or PDF source labels to our GxP-compliant service portal.
We convert unstructured documents into structured content, tagged, with metadata and target XML schema.
Technical schema checks and text verification by our team, built for right-first-time accuracy.
Receive validated XML plus human-readable output, ready for the health authority portal.
Need it faster? Expedited requests can be turned around the same day. We reprioritize to protect your filing deadline.
Why teams come to us
So teams outsource the conversion of their own data. We generate outputs quickly and accurately at production scale, on the same platform we implement for clients, so when you're ready to do it yourself, you can bring it in-house.
Compliant XML at today's volume and structural complexity is beyond most legacy systems.
Teams often outsource while volumes are still low or structured-labeling requirements are still settling.
We run conversions for you on our own platform. When the time is right, bring it in-house and run it yourself.
Proven in production
98%
Right-first-time accuracy
In production conversions with clients.
2–3 days
Standard turnaround
From approved source to validated output.
Same day
Expedited requests
When a deadline can't move, we reprioritize.
Client outcome
A client expected to miss a regulatory filing deadline. We reprioritized, delivered a complex label conversion the same day, and they filed on time.
Production-tested, not theoretical
Our conversion service runs on ComplianceAuthor AI®, the same platform we implement for clients. We use the system, generate the outputs, and submit them to health authorities. So when you bring it in-house, you inherit proven operating workflows you can run from day one.
Explore the platformOur outputs go to real health authority portals.
Vetted against real regulator questions and acceptance criteria.
Proven workflows you inherit when you implement the platform.
A path to greater control
Start with Glemser-run conversions, build internal capability, and move to a full in-house labeling system over time, at your pace, never forced.
Stage 1
Glemser-run conversions
We deliver high-quality, submission-ready conversions using a proven operating model.
Stage 2
Client in-house conversions
You run conversions internally on the platform, building super users and process.
Stage 3
End-to-end labeling system
The platform expands to structured content and full labeling operations.
Tell us your formats, markets, and timelines. We'll scope a conversion plan and protect your deadlines.