We offer comprehensive testing services across all stages of pharmaceutical development:
Ensuring the quality and consistency of your starting materials.
Optimizing product stability and performance.
Verifying that final products meet regulatory specifications.
Assessing product shelf life under various conditions.
Confirming the absence of harmful microorganisms.
Measuring drug levels in biological matrices.
Detailed profiling of active ingredients and excipients.
Ensuring products are free from harmful contaminants.
Supporting formulation effectiveness and regulatory submissions.
Evaluating container integrity and product stability in packaging.
Comprehensive evaluation to support regulatory filings.
We collaborate with a diverse range of laboratories across Europe, Asia, and beyond. This global reach allows us to select the most suitable facilities for your specific needs, whether for early-stage development or commercial-scale production.
Our partners adhere to Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards, ensuring the integrity and reliability of your test results.
We recognize the importance of planning ahead in the pharmaceutical industry. Our team is committed to providing you with all relevant information as soon as it becomes available, ensuring you have the details you need to make informed decisions and maintain your project timelines.