Expert data management system for the 21st century in particulate & defect tracking.

InQuest Science troubleshoots product defect issues and provides training and guidance on particulate matter control, optimized inspection and 21CFR part 11 compliant electronic particulate and physical container/closure defect tracking systems. Focusing on Parenteral, Ophthalmic and Medical Devices to achieve a robust product lifecycle knowledge and control basis. These standardized systems are designed to assure routine particulate and defect control compliance for raw materials, API, incoming single use materials, primary components, 100% in-process inspection and AQL inspection meeting USP<1790>, USP<790>, USP<787>, USP<788> and USP<789> requirements.

In addition, we have developed logical control processes for inspector training and qualification standards management which is unsurpassed in the industry. All this, in conjunction with the appropriate forensics for defect identification and CAPA remediation leads to a high degree of sophistication in day to day process monitoring.

Be a leader in the eyes of the FDA with InQuest Science’s defect management software. Take the next steps into the future of Pharma 4.0.

Are you still working with paper and Excel spreadsheets?

Are you barcode blinding your test kits?

Is your defect library stored in a digital database?

Did you know The Identifier software will:

  • Eliminate paper scattered around multiple departments.
  • Centralize all data in one relational database.
  • Organize your blinded test kits.
  • Store your defect library so it is accessible from anywhere.

Schedule a free demo!

FEATURED VIDEOS

2:47 InQuest - Identifier
Why Choose The Identifier Software?

Unlock Pharma 4.0 for injectable drug inspection. Learn about a system that transforms data management, offering immediate access and global regulatory compliance.

CONTACT INFORMATION

InQuest Science

617 Stokes Rd STE 4334

Medford, NJ 08055

UNITED STATES

Phone: 855-522-2100

FEATURED INSIGHTS