Active Pharmaceutical Ingredients (APIs)
Bulk active substances from certified manufacturers, supplied against specification.
Bulk active substances supplied against a specification with a certificate of analysis, from manufacturers holding the regulatory documentation your filing requires. What decides a source is rarely the assay figure — it is the impurity profile and whether the DMF or CEP you need actually exists.
- Import, delivery and installation
- IQ/OQ and calibration by our Technical Services Division
- Genuine spares and operator training in Dhaka
Specifications
Specifications vary by model and configuration — the brochure carries the full range. Tell us your throughput, sample type and compliance requirement and we will confirm which model fits.
Download the brochure (PDF · 4 KB)Compliance & qualification
Manufactured under ICH Q7 GMP for active substances; the documentation package is confirmed per product.
Applications
Commercial manufacture, formulation development, method development and validation.
Also in Pharmaceutical Standards & Specialty Chemicals
Related products
Secondary & Working Standards
Standards qualified against a primary reference for routine analytical use.
Analytical & Impurity Standards
Characterised impurity and degradation-product standards for method development.
Drug Intermediates
Intermediate compounds used in the synthesis of active substances.