Pharmaceuticals and Herbal Medical Products
DB Lab is approved by the Danish Medicines Agency according to §39 of the Danish Medicines Act to carry
out chemical as well as microbiological analyses of pharmaceuticals, intermediates and raw materials and packaging for pharmaceutical products. The analyses are performed according to the rules of Good Manufacturing Practice (GMP).
DB Lab carries out the analyses according to various phar-macopoeia (Ph.Eur., USP, BP) and in collaboration with our customers, we also develop and validate our own methods (e.g. in accordance with ICH-guidelines). Among other things, the methods are used for product development, registration, stability monitoring, and release.
Our analytical services cover:
- Identification including ID of plastics
- Tests for impurities including residual solvents
- Disintegration tests (tablets, capsules, suppositories)
- Hardness
- Dissolution tests
- Organoleptic tests
- Microbial purity tests
- Quantitative determinations
- Stability monitoring
- Photo stability tests
- Bulk density and tapped density
and a lot more. Call us or send us a mail, if you would like to know more.
