Ensure product safety, efficacy, and regulatory compliance with ºÚÁϲ»´òìÈ’s comprehensive pharmaceutical quality control services for raw materials, active pharmaceutical ingredients (APIs), intermediates, excipients and finished products.
Our consultative, expert scientists provide full analytical development and validation in support of all phases of product and process development, from raw material testing to commercial batch release. Our GMP-compliant and FDA-registered laboratory facilities are fully equipped with a wide range of advanced instrumentation and support a complete offering of analytical outsourcing solutions, including failure analysis, problem-solving, and extractable and leachable testing at any stage of product development.
Quality control testing services
- Analytical method development and validation
- Compendial and monograph testing (USP, EP, BP, JP & ICH)
- Method verification
- Raw material testing
- QC testing of excipients
- In-process sample analysis
- Finished product, batch, and lot release testing
- Stability studies, including ICH stability testing and storage
- Photostability studies and photodegradation
- Forced degradation studies
- Impurity and contamination analysis
- Cleaning validation and environmental monitoring
- Extractables and leachables (E&L) studies
- Analytical support for all stages of CMC development
- Analytical trouble-shooting
- Technology transfer
The ºÚÁϲ»´òìÈ advantage
Our goal is to help you successfully navigate the product development lifecycle and satisfy regulatory standards to bring the highest quality, most efficacious products to market quickly and efficiently. Whether it is for compendial testing or the development and validation of phase-appropriate analytical methods, ºÚÁϲ»´òìÈ’s flexible, customized, and comprehensive testing quality control testing programs are key to ensuring the success of your final product.
To learn about our pharmaceutical quality control testing services, or to speak with one of our experts, contact us today.
More from ºÚÁϲ»´òìÈ
ºÚÁϲ»´òìÈal Impurity Testing and Analysis
ºÚÁϲ»´òìÈ’s trace metal laboratories provide expert elemental impurities testing and analysis in compliance with USP and ICH Q3D guidelines to ensure the safety of drugs and drug products.
NMR Spectroscopy
NMR spectroscopy in pharmaceutical analysis enables identification of substances and impurities, verification of chemical synthesis and compound characterization, supporting critical stages of pharmaceutical development.
Residual Solvents Testing – USP 467 and ICH Q3C
ºÚÁϲ»´òìÈ’s residual solvents testing services per USP 467 and ICH Q3C ensure product quality and safety.
Pharmaceutical Unknown Identification and Impurity Testing
Our experts are experienced across a range of pharmaceutical impurity testing and contaminant analysis, from elemental impurities to extractables and leachables, supporting the safe development of new products.