PHARMACEUTICAL MANUFACTURING TURNKEY SOLUTIONS

End-to-end pharma plants, engineered for global compliance.

AVILOG Global Limited is a world-class provider of fully integrated turnkey solutions for pharmaceutical manufacturing. We design, supply, and coordinate ready-to-operate facilities across Africa, Asia, and the Middle East that meet WHO, cGMP, EU, and FDA standards.

About AVILOG Global Limited

Based in Mauritius with an execution network across India and globally, AVILOG Global Limited specializes in delivering comprehensive solutions for pharmaceutical, biotechnology, nutraceutical, and healthcare manufacturing industries.

Our core strength lies in integrating engineering, equipment, cleanroom technology, validation, and project execution into one seamless solution—reducing risk, cost, and complexity for our clients.

We serve both private sector investors and government institutions, supporting pharmaceutical manufacturing growth, import substitution programs, and national healthcare expansion initiatives.

What we deliver

  • Greenfield & brownfield pharma facilities
  • GMP-compliant cleanrooms & utilities
  • Integrated production & packaging lines
  • QC & microbiology laboratories
  • Regulatory-ready documentation & validation

Turnkey Solution Capabilities

From concept to commissioning, AVILOG acts as a single integrator for every technical and regulatory aspect of your pharmaceutical manufacturing facility.

1. Facility Design & Engineering

We create complete architectural and engineering plans for new builds, expansions, and retrofits:

  • Conceptual & detailed engineering
  • Process flow design
  • Architectural layouts & GMP zoning
  • Structural, mechanical, electrical & plumbing (MEP) engineering
  • HVAC, cleanroom, and utility load calculations
  • Equipment integration design
  • Regulatory design compliance for WHO / GMP / EU

2. Cleanroom & Controlled Environments

We provide end-to-end cleanroom solutions that support critical pharma processes:

  • Modular cleanroom construction
  • HVAC, filtration, and air-handling systems
  • Environmental monitoring & pressure zoning
  • GMP-compliant materials and finishes
  • Epoxy flooring, covings, and sanitary fittings

Cleanroom applications:

  • Oral solid dosage (OSD)
  • Liquid & semi-solid production
  • Injectables & aseptic areas
  • Microbiology & QC labs
  • Packaging halls & warehouse handling zones

3. Pharmaceutical Production Equipment

AVILOG supplies, installs, and validates best-in-class pharmaceutical machinery for:

  • Tablets & capsules production
  • Granulation, compression, coating & polishing
  • Liquid oral formulations
  • Blister packaging & cartoning lines
  • R&D and IPQC equipment
  • Barcode, serialization & track-and-trace systems

We work with leading manufacturers globally to ensure high reliability, automation, and efficiency.

4. QC & Microbiology Laboratories

We design and equip fully compliant QC and microbiology labs for:

  • Analytical chemistry & assay testing
  • Stability & dissolution testing
  • HPLC, FTIR, UV-VIS, GC & related instrumentation
  • Microbial testing, sterility & environmental monitoring

We ensure laboratories meet current Good Laboratory Practices (GLP) and regulatory requirements.

5. Utility Systems Integration

We supply and integrate all essential utilities for a modern pharma plant:

  • Purified water systems (RO / EDI / distribution loops)
  • Steam boilers & compressed air systems
  • Chillers, cooling towers & HVAC utilities
  • Standby power & industrial generators
  • Clean steam, nitrogen, vacuum & process gases

Our turnkey approach ensures utilities are engineered for maximum uptime and energy efficiency.

6. Electrical, Safety & Fire Protection

AVILOG provides integrated electrical and safety systems:

  • Complete electrical distribution networks
  • Control panels & automation systems
  • Lighting & emergency lighting
  • Earthing & lightning protection
  • Fire alarms, hydrants, sprinklers & suppression systems

All systems adhere to NFPA, IEC, and WHO-GMP safety guidelines.

7. Warehouse & Material Handling

We design and equip efficient, GMP-aligned warehousing solutions:

  • GMP-compliant warehouses
  • Racking & shelving systems
  • Cold and humidity-controlled rooms
  • Weighbridges, handling equipment & safety systems

8. Installation, Commissioning & Validation

Our engineers supervise and support all critical start-up activities:

  • Installation of equipment & cleanrooms
  • Utility integration
  • Calibration & functional testing
  • Commissioning protocols (IQ, OQ, PQ)
  • Documentation packages for WHO / GMP regulatory audits

We ensure your plant is ready for licensing, inspection, and full-scale production.

9. Project Management & Approvals

We manage the full project lifecycle for predictable delivery:

  • Site planning & execution scheduling
  • Vendor coordination & expediting
  • Design-build supervision
  • Validation documentation
  • Support for regulatory submissions and licensing

10. After-Sales Support & Services

Beyond commissioning, AVILOG remains a long-term partner:

  • Spare parts & preventive maintenance
  • Annual service contracts
  • Technical training for operators & engineers
  • Remote support & site visits

Industries We Serve

AVILOG supports a broad spectrum of life-science and healthcare manufacturing clients.

Pharmaceutical manufacturers Government medical supply agencies Contract manufacturing organizations (CMOs) Nutraceutical & herbal companies R&D centers and laboratories Healthcare manufacturing initiatives

Our Approach

A structured, engineering-led model that takes projects from vision to validated operation.

  1. 1. Understand Client Vision

    We define capacity, regulatory targets, investment level, and product mix.

  2. 2. Engineer the Manufacturing Ecosystem

    We design facility layouts, cleanrooms, utilities, equipment, and automation as a single integrated system.

  3. 3. Manufacture, Procure & Integrate

    We coordinate global supply, fabrication, and delivery of all equipment and systems.

  4. 4. Supervise Installation & Commissioning

    Our engineers ensure safe installation, testing, and performance verification.

  5. 5. Validate & Prepare for Regulatory Approval

    We support documentation, training, and audit readiness for WHO, GMP, and other authorities.

Why AVILOG Global Limited?

  • Complete turnkey integrator—from concept to commissioning
  • Deep expertise in emerging market pharmaceutical manufacturing
  • Compliance with WHO, GMP, EU-GMP, PIC/S, and FDA guidelines
  • Access to globally reputable equipment manufacturers
  • Strong engineering & project management capability
  • Transparent delivery timelines
  • Efficient cost structures and value-driven solutions
  • Global execution experience with local understanding

Contact Us

Share your project vision, and our team will help you define the optimal path to a fully compliant pharmaceutical manufacturing facility.

AVILOG GLOBAL LIMITED

Unit 5ABC, 5th Floor, Standard Chartered Tower
19 Cybercity, Ebene, Mauritius

Email: info@avilogglb.com

Website: www.avilogglb.com

Phone: +230 (to be updated)

Project Enquiries

Provide a brief overview of your facility requirements:

  • Location & project stage
  • Target dosage forms & capacity
  • Regulatory markets (local / export)
  • Expected go-live timeline

Our team will respond with an initial concept and engagement model.