Your full-service pharmaceutical packaging partner
- One partner for the full journey, from primary to secondary
- Design, components, secondary packaging, serialisation, GDP-ready shipping
- GMP licensed, FMD compliant, Schedule I and II controlled substances
A partner for the programmes most CDMOs avoid
Most pharma teams do not need another commodity supplier. They need one partner who turns a demanding brief into a market-ready pack without months of escalation: specialised packaging for orphan drugs, specialty pharma, medical devices and controlled substances. We have done exactly that since 1996 from Echt, the Netherlands, with 40 specialists on your programme from first prototype to commercial release.
The full packaging journey, coordinated for you
From design we engineer your pack for manufacturability and take care of the whole journey, from primary to secondary. Wallets, blister cards, cartons, kits, titration packs, clinical trial packaging and child-resistant formats through our patented Locked4Kids platform, plus medical device packaging. Cold seal, the sealing technique we pioneered in 1996, runs on most programmes. Serialisation and aggregation run on every line, so EU FMD and US DSCSA are handled without disrupting lead time.
Short lines, decisions at project speed
Scalability is where niche suppliers fail. We run manual and automated lines in one facility, so a clinical trial batch and a commercial launch live on the same system. No fixed minimum order, prototypes in 5 to 10 working days, direct QA access. You work with the people who build the pack, not a broker.
Built for complex programmes, not commodity throughput
Large CDMOs grow rigid around scale; small suppliers lack the GMP, GDP and FMD infrastructure for a regulated launch. Ecobliss sits in between: one agile partner, fast to pick up and fast to first concepts. Locked4Kids, our patented child-resistant platform, is our own IP, and we supply the packaging machine if you would rather insource.
What to expect when you work with Ecobliss
Step 1. Packaging assessment within one week
Share your brief and constraints. Within a week you receive format options, materials, serialisation setup and indicative timelines.
Step 2. Prototype in 5 to 10 working days
Our in-house design team builds a functional prototype so you can validate usability and artwork before tooling.
Step 3. Clinical to commercial on one system
Clinical batches and commercial volumes run on the same qualified lines. No fixed minimum, serialisation and aggregation included as standard.
Step 4. GMP production and GDP-ready release
GMP production, FMD serialisation, GDP warehousing and release for EU, US and RoW. One partner, one point of accountability.
Ready for a packaging partner who speaks your complexity?
Let us assess your programme and show you what one full-service partner can deliver. Call plus 31 475 390 550 or request your packaging assessment.
Frequently asked questions from pharma procurement
Are you a CDMO or a packaging specialist?
We are a specialist packaging partner, service and supplier in one, covering the full journey from primary to secondary. We do not handle API, formulation or QP release. We design, source components, run secondary packaging and serialisation, from clinical to commercial scale, as one accountable partner.
What type of programmes fit Ecobliss best?
Complex, high-value, low to mid volume packaging. Orphan drugs, specialty pharma, medical devices, controlled substances, child-resistant formats and adherence packs. If your programme needs engineering input and regulatory discipline, you are in the right place.
Do you handle serialisation and EU FMD compliance?
Yes. Serialisation and aggregation run on every line. We are fully FMD compliant for the EU and support DSCSA for the US, plus market-specific variants.
Is there a minimum order quantity?
No fixed minimum. Clinical volumes, niche launches and larger commercial programmes run on the same qualified lines.
Can you support controlled substances and child-resistant packaging?
Yes. We are licensed for Schedule I and II controlled substances, and our patented Locked4Kids platform is certified for both the EU and US.
What is your approach to sustainability?
FSC certified board (C194323), water-based solvent-free adhesive for cold seal, and up to 80 percent lower energy use than heat seal.
How do you handle artwork and change control?
Managed by our in-house design team in a blockchain-protected document system, with market-specific variants and regulated change control as standard.
Contact the team
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