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Testing and release for pharma and life sciences

Lab test
Healthcare & Pharma

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:

  1. Sign a mutual CDA/NDA (if applicable)

  2. Share your analytical methods and product specifications

  3. 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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