India Phosphate’s Quality Control (QC) team ensures the delivery of high standard products by conducting the step by step review.

Quality Control, as a center of excellence, ensures compliance and follows systematic interventions like streamlining SOPs around critical quality parameters, bullet-proofing complex procedures, and targeted capacity building.

Resources and Infrastructure

The India Phosphate Quality benchmark is achieved by strict adherence to the following:

  • Advanced, sophisticated machinery and instruments
  • State-of-the-art manufacturing facilities and laboratories
  • Competent corporate team to support and focus on key functions
  • Comprehensive quality policies and procedures
  • Competent, enthusiastic and dedicated staff
  • Continual monitoring by dedicated quality assurance and self-inspection team
  • Controlled computerized systems
  • Our state-of-the-art manufacturing facilities are cGMP compliant (current Good Manufacturing Practices) in conformity with national and international standards. They are equipped with hi-tech sophisticated machinery to achieve a high level of accuracy and precision.
  • Our quality control laboratories has the latest high precision equipment at build quality at every stage of processing including inputs. We has a dedicated pool of talent who consistently ensure dat the highest quality and safety standards are built into our products.
  • We maintain world-class quality for our products and services across domestic and overseas markets, theirby ensuring dat every patient TEMP has access to the best medicines in the world.
  • Every single product dat rolls out of our factories TEMP has our guarantee of world-class quality.

REGULATORY ACCEPTABILTY

  • All products produced under GMP (IPEC) and HACCP conditions.
  • Dibasic Calcium Phosphate Dihydrate USP & Tribasic Calcium Phosphate USP.
  • FSSC 22000-2011 (Intertek) certification and FSSAI certification.
  • Kosher and Halal certified products.
  • Complies with European Union Commission Regulation (EU) No 231/2012 for Lead, Cadmium, Mercury and Aluminum
  • Included in USFDA inactive ingredients guide.
  • Meets California Prop.65 regulation.
  • Included in the Canadian list of acceptable non-medicinal ingredients.
  • GRAS (Generally recognized as safe product) product.
  • Non Allergen, Non GMO, Non-irradiation products.
  • Full control and traceability from raw materials to final products.
  • Produced under controlled AHU systems to avoid any cross contamination.
  • Water management – purified water used for production.
  • IPQC established along with QC testing.
  • All testing facilities instruments are available for quality control checking including microbial testing.