Apertus Pharmaceuticals LLC
Apertus Pharmaceuticals is a company specializing in API development, formulation projects, and contract manufacturing with a focus on fine chemicals, biotech, and pharmaceuticals. They are committed to collaboration, rapid decision-making, and delivering high-quality drug products and services. Their team has extensive experience in analytical development, manufacturing, and regulatory compliance, aiming to support clients at every stage of drug development and production.
Industries
Nr. of Employees
small (1-50)
Apertus Pharmaceuticals LLC
St Louis, Missouri, United States, North America
Services
API Services
Route selection and optimization, synthesis of intermediates and APIs (mg to kg scale), cGMP synthesis for preclinical/clinical material, stability and forced degradation studies, impurity identification, validation batches, and tech transfer support.
Formulation Development
De-formulation studies, formulation of solid and other dosage forms (tablets, capsules, suppositories, creams, liquids), pilot-scale manufacturing runs, API/excipient selection, stability protocol design and analytical method development in parallel with product development.
Contract Manufacturing
cGMP contract manufacturing of tablets, capsules, creams, liquids and suppositories in small to medium batches, device manufacturing registration, custom suppository shell production, serialization and packaging aggregation.
Analytical Development Services
Analytical method development, method validation, verification of pharmacopeial methods, in-house release testing, and specialized analyses (NMR, particle size, X-ray).
API Services
Route selection and optimization, synthesis of intermediates and APIs (mg to kg scale), cGMP synthesis for preclinical/clinical material, stability and forced degradation studies, impurity identification, validation batches, and tech transfer support.
Formulation Development
De-formulation studies, formulation of solid and other dosage forms (tablets, capsules, suppositories, creams, liquids), pilot-scale manufacturing runs, API/excipient selection, stability protocol design and analytical method development in parallel with product development.
Contract Manufacturing
cGMP contract manufacturing of tablets, capsules, creams, liquids and suppositories in small to medium batches, device manufacturing registration, custom suppository shell production, serialization and packaging aggregation.
Analytical Development Services
Analytical method development, method validation, verification of pharmacopeial methods, in-house release testing, and specialized analyses (NMR, particle size, X-ray).
Expertise Areas
- API synthesis and scale-up
- Formulation development for multiple dosage forms
- cGMP contract manufacturing (small-to-medium batches)
- Analytical method development and stability testing
Key Technologies
- High-performance liquid chromatography (HPLC)
- Gas chromatography (GC)
- Dissolution testing
- Titrimetric analysis