TajMedico is a science-driven pharmaceutical organization committed to delivering safe, effective, and high-quality medicines through a robust Quality Control (QC) system. The company ensures that every product released to the market meets strict national and international regulatory standards, including WHO-GMP, IP, USP, BP, and ICH guidelines.

At the heart of TajMedico’s manufacturing excellence lies its well-equipped Quality Control laboratory, designed to perform comprehensive testing of raw materials, in-process samples, and finished products. The QC system ensures complete assurance of purity, potency, safety, and consistency across all pharmaceutical formulations.

🔬 Advanced QC Laboratory Infrastructure

TajMedico’s QC lab is equipped with modern analytical instruments such as:

  • High-Performance Liquid Chromatography (HPLC)
  • Gas Chromatography (GC)
  • UV-Visible Spectrophotometer
  • FTIR Spectroscopy
  • Dissolution & Disintegration Test Apparatus
  • Hardness, Friability & Thickness Testers
  • Microbiological Testing Facilities

These systems ensure precise, reliable, and reproducible testing results for all dosage forms.

💊 Quality Control for OSD & External Preparations

Oral Solid Dosage (OSD)

Includes tablets, capsules, granules, and pellets.

Key QC Tests:

  • Assay of active ingredients
  • Content uniformity
  • Dissolution profiling
  • Hardness & friability
  • Moisture analysis
  • Stability testing

External Preparations

Includes creams, ointments, gels, lotions, and liquids.

Key QC Tests:

  • pH and viscosity analysis
  • Homogeneity & spreadability
  • Microbial limit testing
  • Preservative efficacy testing
  • Stability and compatibility studies

⚙️ In-Process Quality Control (IPQC)

TajMedico ensures real-time monitoring during production to maintain consistency and prevent deviations. Key parameters include:

  • Blend uniformity
  • Granulation quality
  • Tablet weight variation
  • Coating uniformity
  • Filling accuracy for topicals

This proactive system ensures zero-defect manufacturing approach.

📊 Stability Studies & Regulatory Compliance

All products undergo accelerated and long-term stability studies as per ICH guidelines to determine shelf life, storage conditions, and product performance over time.

Every batch is released only after:

  • Full analytical testing
  • QA approval
  • Compliance verification
  • Documentation review (CoA, BMR, BPR)

👩‍🔬 Skilled Quality Team

TajMedico’s QC division is managed by highly trained professionals including:

  • Analytical Chemists
  • Microbiologists
  • Quality Assurance Experts
  • Validation Specialists

Continuous training ensures alignment with evolving global regulatory standards.

🌍 Commitment to Global Quality Standards

TajMedico operates under a Quality by Design (QbD) approach, ensuring every product is:

✔ Safe for patients
✔ Consistent in performance
✔ Compliant with global regulations
✔ Manufactured with precision and control

Contact Details – TajMedico

Corporate Office:
TajMedico India Limited
Mumbai, Maharashtra, India

Manufacturing Facility:
Sarigam GIDC Industrial Area
Gujarat, India

Business Enquiry Email:
📧 info@tajpharma.com
📧 tajgroup@tajpharma.com

Phone:
📞 +91-7400009975/76 (Sales & Business Support)