QC Chemical Analysis
Comprehensive analytical testing for your pharmaceutical needs
QbD Group's GMP-certified QC laboratory provides reliable and accurate chemical analysis services for raw materials, APIs, IMPs, and finished medicinal products.
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 include:
- Pharmacopoeial testing: Verifying compliance with pharmacopoeial standards.
- Finished products: Testing for compliance with regulatory dossier.
- Advanced instrumentation: Using state-of-the-art technology to deliver precise results.
- Regulatory compliance: Ensuring methods align with GMP and other requirements.
Why is QC chemical analysis important?
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?
Our QC laboratory offers a wide range of chemical analysis services, including:
Identification tests
IR, TLC, and HPLC with multiple detectors.
Appearance testing
Assessing color and clarity.
Assays
Utilizing UV/Vis, automatic titration, HPLC/UHPLC, and GC techniques.
Dosage uniformity testing
Ensuring consistent dosing in medicinal products.
Impurity testing
Quantifying related substances, residual solvents, and elemental impurities.
Physical determinations
Measuring pH, viscosity, density, and more.
Solid oral dosage tests
Including disintegration, dissolution, hardness, and friability.
Specialized testing
DSC, TOC analysis, laser particle size distribution, and particulate matter evaluation.
Our process
We follow a structured approach to deliver reliable, GMP-compliant analytical results.
1. Consultation
Understanding your analytical needs and product requirements.
2. Method selection
Choosing the optimal analytical approach for your samples.
3. Analysis
Executing tests using advanced instrumentation under GMP conditions.
4. Reporting
Delivering comprehensive results with regulatory-compliant documentation.
Why QbD Group
Your trusted partner
When you partner with QbD Group for QC chemical analysis, you gain:
Comprehensive expertise
from general identification to advanced impurity testing, we cover a broad spectrum of analytical needs.
GMP certification
a licensed laboratory capable of handling psychotropics, narcotics, hormones, and highly potent products.
Advanced equipment
cutting-edge technology for precise and efficient testing.
Flexible support
full-service analysis to help you focus on your core business.
Regulatory assurance
services designed to meet global compliance standards.
Let's talk Lab Services
From method validation to stability testing, our lab experts are ready to support your analytical needs.