Quality Control
Our rigorous testing and verification processes confirm that pharmaceutical products meet all quality standards before release to the market.
At Sovvaka Global, quality control represents the final verification step in our comprehensive quality system, ensuring that only products meeting our stringent quality standards reach patients and healthcare providers.
Comprehensive Quality Testing
Our quality control laboratories employ a wide range of testing methods to ensure pharmaceutical products meet all specifications and quality standards.
Physical Testing
Evaluation of physical properties such as appearance, color, odor, particle size, dissolution rate, and hardness to ensure product consistency.
Chemical Analysis
Precise determination of chemical composition, including assay of active ingredients, impurity profiling, and content uniformity testing.
Microbiological Testing
Assessment of microbial contamination, sterility, and antimicrobial effectiveness to ensure product safety and stability.
Stability Testing
Evaluation of product stability under various environmental conditions to confirm shelf life and storage requirements.
Instrumental Analysis
Advanced analytical techniques including HPLC, GC, UV spectroscopy, and mass spectrometry for precise quantitative and qualitative analysis.
Packaging & Labeling Inspection
Thorough examination of packaging integrity, label accuracy, and product information compliance with regulatory requirements.
Quality Control Process
Our systematic quality control process ensures thorough evaluation of pharmaceutical products at every critical stage.
Sampling
01Statistical sampling of raw materials, in-process materials, and finished products according to established sampling plans to ensure representative testing.
Testing
02Comprehensive testing using validated analytical methods to evaluate product characteristics against predetermined specifications.
Data Analysis
03Thorough analysis of test results using statistical methods to ensure accuracy, precision, and reliability of findings.
Compliance Evaluation
04Assessment of test results against established specifications and regulatory requirements to determine product compliance.
Documentation
05Comprehensive documentation of all testing activities, results, and conclusions in accordance with GMP requirements.
Release Decision
06Final review and approval by qualified personnel to authorize product release based on complete quality control data.
Laboratory Capabilities
Our state-of-the-art quality control laboratories are equipped with advanced analytical instruments and staffed by highly qualified scientists to ensure accurate and reliable testing.
Advanced Instrumentation
Our laboratories feature cutting-edge analytical equipment including HPLC, GC-MS, FTIR, UV-Vis spectrophotometers, and dissolution testers for comprehensive product analysis.
Specialized Testing Areas
Dedicated areas for microbiological testing, stability studies, and physical testing ensure optimal conditions for each type of analysis.
Expert Personnel
Our team of experienced analysts and microbiologists possesses specialized knowledge in pharmaceutical testing methods and regulatory requirements.
Method Development & Validation
Capabilities for developing and validating analytical methods tailored to specific product requirements, ensuring accurate and reliable testing.
Benefits of Our Quality Control System
Our comprehensive quality control system provides numerous benefits that ensure product quality and patient safety.
Product Consistency
Ensures batch-to-batch consistency through rigorous testing against established specifications and standards.
Patient Safety
Protects patient health by verifying product safety, potency, and purity before market release.
Regulatory Compliance
Facilitates compliance with regulatory requirements through comprehensive testing and documentation.
Early Issue Detection
Identifies potential quality issues early in the process, preventing costly recalls and market withdrawals.
Data-Driven Decisions
Provides objective data for informed decision-making regarding product release and continuous improvement.
Brand Protection
Safeguards brand reputation by ensuring only high-quality products reach customers and patients.
Learn More About Our Quality Control
Contact our quality team to learn more about our quality control processes and how they ensure the highest standards for pharmaceutical products.
Our Quality Control Expertise
- Pharmacopoeial testing (USP, BP, EP, IP)
- Method development and validation
- Stability testing and monitoring
- Microbiological testing
- Advanced analytical techniques