Method development & validation
Quantification methods for active substances and preservatives, plus related-substances methods — developed and validated to current pharmacopoeial expectations.
Laboratory & analytical services
The analytical laboratory that supports our own GMP production also takes on external work. From method development to stability studies, our chemists and chemical engineers run the tests your dossier or your batch release needs.
What we can run for you
Dissolution testing
Dissolution method development and validation for oral solid and powder forms.
Stability studies
Long-term and accelerated stability programmes, with the storage conditions and pull points agreed up front.
Quality-control testing
Routine physicochemical QC testing on raw materials, in-process samples and finished product.
Why our laboratory
- The same laboratory releases every batch we manufacture — 100% batch-based quality control under GMP discipline.
- Staffed by chemists, chemical engineers and biologists within a 120+ specialist team.
- R&D projects run in partnership with TÜBİTAK.
- Experience with dossier-grade analytical data for products exported to 40+ markets.
Scope, turnaround and pricing are agreed per project. Tell us what you need tested and we will confirm what we can take on.
Request analytical services
Describe the samples and the tests you need — our laboratory team will respond with feasibility, turnaround and pricing.