At ARSI Canada Inc., we offer comprehensive forced degradation studies designed to assess the stability and degradation pathways of drug substances and products.
Forced degradation studies involve subjecting samples to stress conditions such as heat, light, humidity, and acidic or alkaline pH to accelerate degradation
processes and identify potential degradation products.
Forced degradation studies play a critical role in pharmaceutical development and regulatory submissions:
Provides crucial data on the stability of drug substances and products under various stress conditions, guiding formulation development and shelf-life determination.
Helps identify degradation pathways and potential degradation products, enabling the development of robust formulations and manufacturing processes.
Supports regulatory submissions by demonstrating product stability, ensuring compliance with regulatory guidelines (e.g., ICH Q1A), and justifying proposed storage conditions and shelf-life specifications.
Facilitates risk assessment by identifying potential degradation-related risks and enabling the implementation of appropriate mitigation strategies.
ARSI Canada Inc. is your trusted partner for forced degradation studies, offering:
Our team of scientists has extensive expertise in forced degradation studies and stability testing.
We utilize state-of-the-art instrumentation and techniques to conduct forced degradation studies with precision and accuracy.
We are well-versed in global regulatory requirements, ensuring that our studies meet the highest standards of quality and compliance.
We provide detailed reports summarizing study findings, degradation pathways, and recommendations for formulation optimization and stability testing.
We conduct degradation studies to understand the stability of drug substances and products, identifying potential degradation products and their impact
We conduct stress testing studies to evaluate the stability of drug substances and products under various stress conditions, including:
We identify and characterize degradation products using advanced analytical techniques, including:
Choosing ARSI Canada Inc. for your forced degradation study needs means partnering with a team dedicated to delivering accurate, reliable, and actionable data. Our experienced scientists, advanced instrumentation, regulatory expertise, and comprehensive reporting ensure that your forced degradation studies are conducted with precision and expertise, supporting your drug development and regulatory submission requirements.
Get in touch with ARSI Canada Inc. for comprehensive forced degradation study services and ensure the stability and safety of your drug substances and products.
We clarify targets, specs, safety, and timelines; align on success criteria and CDA/IP terms.
Route scouting, risks, and costed plan with deliverables, data package, and milestones.
Synthesis, in-process controls, purification, and analytical verification at each stage.
Materials shipped per spec with full documentation and optional tech transfer support.
Share your target, quantity, and timeline — we’ll return a clear, cost-effective proposal.
We operate with rigorous QC, data integrity, and traceability aligned with international guidelines. Every shipment includes complete analytical documentation and batch records.
Explore our range of specialized solutions designed to support your unique needs with quality, reliability, and expertise.
