Quality Control
Area of Expertise
At Alapati Pharma, we prioritize quality, efficacy, and purity in every product we manufacture. Our commitment to excellence is reflected in our stringent quality control (QC) and quality assurance (QA) processes, ensuring compliance with global regulatory standards.
Comprehensive Quality Control & Assurance
- Expert Analytical Team Our highly skilled team of professionals specializes in analytical procedures, ensuring that every product meets strict quality specifications at every stage of production.
- Stringent Raw Material & Excipient Testing
- We source all raw materials and excipients exclusively from approved vendors to maintain consistency and quality.
- Every material undergoes thorough analysis at the initial stage before being used in production.
- In-Process Quality Checks
- Each product is monitored and analyzed at every stage of manufacturing to ensure it meets the required specifications and quality parameters.
Our facility is equipped with state-of-the-art analytical instruments, including:
- HPLC (Shimadzu / Agilent) – For precise quantitative analysis of drug components.
- Dissolution Apparatus (8 Phase) – To study drug release profiles.
- Disintegration Apparatus – To evaluate tablet and capsule breakdown time.
- Spectrophotometer – For accurate material identification and purity assessment.
- IPQA & IPQC Equipment – To monitor quality in real-time during production.
Stability Testing & Validation
To ensure precision, efficacy, and enhanced patient compliance, we implement a variety of cutting-edge pharmaceutical technologies based on product classification, including:
- Dedicated Sampling Booth & Stability Chambers
- We conduct accelerated and long-term stability studies to ensure that our products maintain efficacy and quality throughout their shelf life.
- Complete Process & Product Validation
- Every commercially manufactured product undergoes extensive validation, ensuring consistent quality and compliance with industry standards.
