Quality Assurance Policy
As a manufacturer of bulk drugs, intermediates and fine chemicals, we at Supriya Lifescience, have a moral and social responsibility to ensure the highest quality from process to product. We are committed to driving the growth of our organisation by continually enhancing customer satisfaction, by providing a safe and congenial working environment to employees and by treating suppliers as business partners.

Quality Assurance
At Supriya Lifescience, we take our commitment to Quality very seriously. Every plant has well defined processes and systems in place, to comply with Current Good Manufacturing Practices (cGMP) laid down by Schedule M, Schedule L, ICH Q7 and TRS guidelines.

Well-defined Standard Operating Procedures (SOPs) and protocols have been documented and implemented for our quality system based on the various guidelines laid down by regulatory bodies WHO, PIC’s and EU GMP . These are reviewed at regular intervals to keep pace with global standards.

  • Our processes , cleaning , analytical method transfers & technology are all validated by regulatory authorities.
  • All Vendors and Contract Laboratories are subject to the most demanding global quality standards.
  • However , our toughest challenge is to meet our own internal Quality Standards. We set the bar for ourselves much higher than those set by International Regulatory bodies

Quality Control

  • A dedicated Quality Control Department is committed to setting the gold standard for quality in every aspect- processes , systems and products.
  • They are helped in their mandate by a State-Of-the-Art Quality Control laboratory complex spread over an area of 10,000 sq.ft.
  • The Laboratory is equipped with Ultra-modern & Sophisticated High precision instruments like – GC – HS, HPLC with PDA and UV Detectors, Spectrophotometers, Digital Polarimeter, UV Spectrophotmeter, FTIR, ATR, Auto Titrators, Karl Fischer, IR moisture balance, TOC, Autoclave, Incubators, Malvern Particle Size Analyzer, RO – TAP Sieve Analyzer, Bulk Density Apparatus, TLC Analyzer etc
  • The complex includes a Microbiology & Endotoxin testing Laboratory
  • Stability chambers for stability monitoring as per ICH guidelines 25°C-60%RH, 30°C- 65%RH , 35°C- 75%RH & 40°C-75%RH, 60°C
  • Reserve sample management: Storage area with controlled room temperature (Below 25°C).

Our Strength

  • At the core of our success , is our committed and dedicated staff.
  • Every Team member is trained and qualified to play specialised roles in various functional areas
  • Regular training programmes and workshops are conducted to expose them to rapidly evolving global technological changes
  • Attractive career & growth opportunities keep the team energised and inspired
  • A range of welfare measures keep the team motivated and contented