QC Chemical Analysis
Comprehensive analytical testing for your pharmaceutical needs
At QbD Group, our GMP-certified QC laboratory provides reliable and accurate chemical analysis services to meet the demands of the pharmaceutical industry. Whether it’s raw materials, APIs, IMPs, or finished medicinal products, we offer tailored solutions to support your analytical needs. With advanced capabilities and a team of experts, we ensure your products meet the highest standards of quality and compliance.
What is QC chemical analysis?
Quality Control (QC) chemical analysis involves a series of analytical tests and procedures to verify the quality, safety, and efficacy of pharmaceutical products. From raw materials to finished dosage forms, QC chemical analysis ensures compliance with stringent regulatory standards and helps maintain product integrity. Key aspects of QC chemical analysis include:
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Pharmacopoeial testing: Verifying compliance with pharmacopeial standards for raw materials and products.
- Finished products: testing for compliance with regulatory dossier.
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Advanced instrumentation: Using state-of-the-art technology to deliver precise results.
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Regulatory compliance: Ensuring methods align with GMP and other regulatory requirements.
Why is QC chemical analysis important?
QC chemical analysis is critical for:
- Product safety: Ensures pharmaceutical products are free from harmful impurities.
- Regulatory compliance: Meets GMP standards and pharmacopoeial requirements.
- Quality assurance: Confirms the quality and consistency of raw materials and finished products.
- Operational efficiency: Reduces risks of recalls and non-compliance by identifying issues early.
- Process validation: Supports robust manufacturing processes with reliable data.
How can we help?
Identification tests
Appearance testing
Appearance testing
Assessing color and clarity.
Assays
Assays
Utilizing UV/Vis, automatic titration, HPLC/UHPLC, and GC techniques.
Dosage uniformity testing
Dosage uniformity testing
Ensuring consistent dosing in medicinal products.
Impurity testing
Impurity testing
Quantifying related substances, residual solvents, and elemental impurities.
Physical determinations
Physical determinations
Measuring pH, viscosity, density, and more.
Solid oral dosage tests
Solid oral dosage tests
Including disintegration, dissolution, hardness, and friability.
Specialized testing
Specialized testing
DSC, TOC analysis, laser particle size distribution, and particulate matter evaluation.
Why partner with QbD Group?
When you partner with QbD Group for QC chemical analysis, you gain:
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Comprehensive expertise: From general identification to advanced impurity testing, we cover a broad spectrum of analytical needs.
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GMP certification: A licensed laboratory capable of handling psychotropics, narcotics, hormones, and highly potent products.
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Advanced equipment: Cutting-edge technology for precise and efficient testing.
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Flexible support: Full-service analysis to help you focus on your core business.
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Regulatory assurance: Services designed to meet global compliance standards.