Quality Control (QC) Department at Taj Pharma

Ensuring Excellence in Pharmaceutical Manufacturing

Quality Control Department - Taj Pharma
Quality Control Department

The Quality Control (QC) department plays a crucial role in the pharmaceutical industry, ensuring that every product meets the highest standards of safety, efficacy, and quality. At Taj Pharma, our QC department is equipped with state-of-the-art instruments, highly qualified professionals, and stringent standard operating procedures (SOPs) to comply with global pharmaceutical regulations.

Primary Quality Control Equipment for Pharmaceutical Finished Formulation Manufacturing

1. High-Performance Liquid Chromatography (HPLC)

HPLC is used for accurate analysis of active ingredients, impurities, and stability testing in tablets, capsules, and liquid formulations to ensure correct potency and purity.

2. Gas Chromatography (GC)

GC helps analyze volatile substances and residual solvents in pharmaceutical products, ensuring compliance with safety and regulatory guidelines.

3. UV-Vis Spectrophotometer

This instrument measures the absorbance of solutions to determine the concentration of active pharmaceutical ingredients (APIs), confirming consistency across different batches.

4. Dissolution Test Apparatus

Essential for ensuring tablets and capsules release active ingredients at the correct rate under simulated stomach conditions.

5. Tablet Hardness Tester

Used to measure the mechanical strength of tablets, ensuring they withstand handling, packaging, and transportation without breaking.

6. Friability Tester

Tests tablet resistance to abrasion during handling, ensuring durability and minimal product loss in bulk production.

7. Disintegration Tester

Ensures tablets disintegrate within a specific timeframe, which is critical for bioavailability and therapeutic efficacy.

8. Moisture Analyzer

Measures moisture content in powders, granules, and creams, preventing microbial contamination and ensuring stability.

9. Microscope and Microbial Testing Equipment

Used for sterility and microbial contamination testing to meet global microbiological safety standards.

10. Viscometer

Measures the viscosity of creams, ointments, and oral jelly, ensuring proper texture and consistency for patient usability.

11. BOD Incubator

Provides controlled environmental conditions for microbial growth testing and stability studies, ensuring sterility compliance.

12. Automated Capsule/Tablet Counting Machines

Ensures accurate counting and packaging of tablets, capsules, and sachets, reducing human error and enhancing efficiency.

13. Stability Chambers

Stores finished products under controlled temperature and humidity conditions to study product stability and shelf life.

14. Particle Size Analyzer

Determines the particle size distribution of dry powders and granules, ensuring uniformity and optimal dissolution rates.

15. Packaging Integrity Tester

Ensures airtight sealing of packaging materials, preventing contamination and preserving product efficacy.

Quality Control Procedures at Taj Pharma

1. Personnel and Expertise

  • Highly Qualified Scientists trained in pharmaceutical chemistry, microbiology, and analytical techniques.
  • GMP and GLP Compliance ensuring regulatory adherence and best practices in quality assurance.

2. Advanced QC Facilities

  • Chemical Testing Labs for raw materials, in-process, and finished product analysis.
  • Microbiological Labs for sterility and endotoxin testing.
  • Stability Chambers for environmental impact studies on product longevity.
  • Dedicated Clean Areas for high-risk material and sterile product testing.

3. Rigorous QC Testing

  • Raw Material Testing: Analysis of identity, purity, and compliance with pharmacopoeial standards.
  • In-Process Control: Monitoring critical parameters like pH, viscosity, and temperature.
  • Final Product Testing: Ensuring compliance with potency, dissolution, and packaging integrity requirements.
  • Microbiological Testing: Sterility, endotoxin, and microbial contamination analysis to prevent patient risk.

4. Documentation & Compliance

  • Comprehensive SOPs for sampling, testing, calibration, and deviation handling.
  • Validation Protocols ensuring instrument validation, method validation, and process validation.
  • Batch Release Documentation confirming compliance with pharmacopoeial and regulatory standards.

5. Regulatory Adherence

  • Good Manufacturing Practices (GMP) ensuring the highest standards of safety.
  • Compliance with International Standards (FDA, EMA, WHO-GMP, and Indian Pharmacopoeia).
  • Regular Audits & Inspections to maintain quality assurance.

Taj Pharma: Commitment to Global Pharmaceutical Standards

State-of-the-Art Manufacturing Facility

  • Located in Sarigam GIDC, Gujarat, India
  • WHO-GMP, PICs, and ISO 9001:2018 Certified
  • EU GMP Approval in Progress

High-Volume Pharmaceutical Production

  • Tablets: 120 million per month
  • Capsules: 40 million per month
  • Dry Powders & Granules: 36,000 kg per month
  • Effervescent Tablets: 20 million per month
  • Oral Jelly: 60 million per month
  • Creams & Ointments: 40 million per month
  • Oral Sachets: 3 million per month

Why Choose Taj Pharma?

  • Uncompromised Quality Assurance
  • Advanced Analytical and Microbiological Testing
  • Stringent Compliance with Global Regulatory Standards
  • Innovative Pharmaceutical Manufacturing Solutions

Contact Information

Manufacturing Plant: TAJ PHARMA INDIA LTD.,
Plot No.1019, Vill. – Sarigam, G.I.D.C.,
Road No. 10, Dist. – Valsad,
Gujarat, India 396155.

WHO-cGMP, GMP, GLP Approved, EU-GMP, PICs, ISO 9001:2018, SGS Certified.

📞 Tel. No.: +91 – 22 – 2637 4592 / +91 -22 – 2637 4593
📠 Fax: +91-22-2634 1274
📞 Mobile: +91 84484 44095

Ensuring Excellence in Pharmaceutical Manufacturing

The Quality Control (QC) department at Taj Pharma is committed to ensuring safety, efficacy, and regulatory compliance in pharmaceutical manufacturing. Equipped with state-of-the-art instruments and highly trained professionals, Taj Pharma adheres to WHO-GMP, PICs, and ISO 9001:2018 standards, with EU GMP approval in progress.

Key QC Equipment and Testing

Taj Pharma’s QC department utilizes advanced analytical and microbiological testing instruments, including:

  • HPLC & Gas Chromatography (GC): Analyze active ingredients, impurities, and volatile substances.
  • Dissolution & Disintegration Testers: Ensure tablets release active ingredients correctly.
  • Microbial Testing Equipment: Ensures sterility and safety.
  • Stability Chambers: Monitor product durability under varying conditions.
  • Tablet Hardness & Friability Testers: Assess mechanical strength and durability.
  • Moisture Analyzer & Viscometer: Maintain consistency in formulations.
  • Automated Counting & Packaging Integrity Testers: Ensure accuracy in packaging.

Quality Control Procedures

  • Raw Material & In-Process Testing: Ensures quality at every production stage.
  • Finished Product Testing: Validates potency, dissolution, and microbiological safety.
  • Regulatory Compliance: Follows GMP, FDA, EMA, and Pharmacopoeial standards.
  • Data Management & Validation: Ensures traceability and accuracy in quality checks.