
Testing and release for pharma and life sciences
Importation Testing
Planning to market a pharmaceutical product in the EU that’s manufactured outside the Union? Importation testing in a GMP-certified laboratory located within the EU is a legal requirement. We are fully equipped to carry out these tests quickly and in full compliance — including support with QP release and registration in countries such as Lebanon.
Why Choose Us?
GMP-compliant, ISO 13485-certified, FDA-registered
WHO-prequalified laboratory
Fast turnaround times and reliable results
Flexible support with or without your own QP
Experience with international regulatory requirements
EU Importation Testing
We offer a comprehensive range of pharmaceutical quality control services, including:
Analytical testing of drug products and raw materials
Microbiological testing and sterility testing
Batch release testing (according to EU regulations)
Support with Qualified Person (QP) release
You can choose to work with your own QP or collaborate with one of the experienced Qualified Persons we partner with.
Want to learn more about how we can support your EU import testing needs? Please feel free to contact us.
Lebanon Registration Testing
WHO prequalified testing for drug registration with the Lebanese Ministry of Health
In addition to EU import testing, we also support companies seeking product registration in Lebanon. The Ministry of Health in Lebanon requires a Certificate of Analysis (CoA) performed by a WHO-prequalified control laboratory — a designation held by Normec Synergy Health.
The process is simple and efficient, with only a few required steps:
Sign a mutual CDA/NDA (if applicable)
Share your analytical methods and product specifications
Request a quote and plan your testing
Our expert team will guide you through the process and ensure fast, compliant testing to support your launch in Lebanon.
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Leading companies in this service

Normec Synergy Health
Nieuwegein Netherlands