Quality Control Department
Presented by: Padsala Bansi Sanjaybhai
Sal Institute of Pharmacy
Quality Control Department
Cropel Lifesciences Pvt. Ltd.
Training Duration: 15/09/2025 – 04/10/2025
Established company in the pharmaceutical and life sciences sector.
Focused on producing quality medicines and healthcare products.
Committed to innovation, safety, and patient well-being.
Pharmaceuticals and life sciences expertise
Dedicated to quality and safety standards
Gain real-world experience in the Quality Control (QC) department.
Understand laboratory practices and documentation procedures.
Learn about testing methods and quality standards.
Exposure to pharmaceutical manufacturing processes
Develop practical skills in quality control
QC ensures the safety, purity, and quality of products before release.
It involves chemical, physical, and microbiological testing.
QC is a key department in every pharmaceutical company.
Crucial for product safety
Testing raw materials and finished products
Separate areas for chemical, instrumental, and microbiology sections.
Strict adherence to lab safety rules: lab coat, gloves, goggles.
Proper waste disposal and instrument maintenance.
Organized lab for efficient testing
Following safety guidelines
High-Performance Liquid Chromatography (HPLC).
UV–Visible Spectrophotometer.
pH Meter and Analytical Balance.
Dissolution and Disintegration Test Apparatus.
Essential analytical tools
Identification tests to verify raw materials.
Assay tests to determine drug content.
Dissolution and uniformity tests for tablets.
Documentation of all results in logbooks.
Verifying quality at each stage
Prepare sample and standard solutions.
Inject into HPLC system and record chromatogram.
Compare sample peak area with standard to calculate assay.
Ensure accuracy and precision of results.
Quantifying drug concentration
Follow SOPs for every test and procedure.
Maintain cleanliness and calibration of instruments.
Ensure data integrity and traceability.
Wear proper protective gear at all times.
Following the guidelines
All tests are recorded in controlled notebooks.
Reports must be reviewed and signed by supervisors.
Data must be traceable and stored safely.
Ensures transparency during audits.
Maintaining accurate records
Understanding complex instruments like HPLC.
Learning proper sample preparation techniques.
Maintaining accuracy in documentation.
Adapting to a professional laboratory environment.
Overcoming learning curves
Improved practical knowledge of analytical techniques