PATIENTS SAY: Jan Spokane WA (Monday, 12 September 2011 04:18)
PATIENTS SAY: Alex Los Angeles, CA (Monday, 12 September 2011 04:17)

Quality Assurance


From each batch of raw materials and additives, samples are evaluated and only approved batches as per applicant current regulatory systems requirements are released for production.Tablet & Capsule samples are checked during processing by a system of operator inspection, which consists or taking random samples at regular intervals. Dimensions, visual defects, moisture content, Color and microbial purity are thus regularly monitored during production, Further sampling inspection is carried out at the final stage. Stringent process control and monitoring ensure consistency, uniformity and conformance to specifications. before the release of each lot, a review is made of all process control documents and records to ensure conformance to in-process control and operator inspection during manufacture

 

  • Material conformity with IP, USP and BP
  • Colorants in conformance with pertinent regulatory systems
  • Adherence to cGMP facilitates manufacture of preservation free capsules
  • Continuous monitoring of critical process parameters and assessment of print quality.
  • Preshipment audit.
  • Low reject rates.