IPS India Capabilities



IPS serves pharmaceutical, biotechnology and medical device and diagnostic companies with worldwide, full-service engineering service dedicated to improve operations, revitalize facilities and stay compliant in a global regulatory environment.

By focusing on technically complex and high performance disciplines, IPS delivers compliance-driven projects that improve operational performance and accelerate time-to-market clients worldwide. In addition, IPS possesses the expertise and the technical know how in Oral Solid Dosage (OSD), Biopharmaceutical and Injectable facilities using potent and cytotoxic compounds.

For over 18 years, our industry-trained professionals have provided:

  • Design
    • Architectural
    • Civil / Mechanical / Process / Electrical / Permitting
    • Conceptual Design
    • Environmental / Effluent Treatment
    • Health and Safety
    • Manufacturing Equipment
    • Automation
  • Technical Consulting
  • Engineering
  • Process Engineering
  • Commissioning & Validation
    • Qualification and Validation
    • Impact Assessments and Master Planning
    • Construction & Design Interface/Review
    • Equipment Selection
    • Project Management
    • Quality System Implementation
    • Calibration System Consulting
    • Audits
      • Quality Systems
      • FDA-Style
      • cGMP
    • Remediation of FDA Form 483s/Warnings
    • Validation and cGMP Training
    • Process and Cleaning Validation
    • Automation and Computer Systems Validation
    • Document Development/Management
      • Specification/SOP Preparation
      • Site/Project Document Control
      • Custom Protocols
      • Factory/Site Acceptance Test
    • 21 CFR Parts 111 and 112, Dietary Supplement Final Rule
    • Whole Building Commissioning
    • LEEDŽ Commissioning
    • Maintenance and Reliability Programs
    • Energy Studies
    • RetroCommissioning