solution by Industry

End-to-End Pharmaceutical Manufacturing Solutions Built to Global GMP Standards

From IV infusion lines to oral solid dosage plants — IVEN delivers turnkey pharmaceutical production systems trusted across 70+ countries.

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Industry Overview

The Industry at a Glance

The global pharmaceutical manufacturing market is projected to exceed $1.5 trillion by 2028, driven by rising demand for injectable drugs, biologics, and generic medicines in emerging markets. Governments worldwide are tightening GMP compliance requirements, pushing manufacturers to upgrade aging facilities and adopt automated, validated production lines. For pharmaceutical companies scaling capacity or entering new markets, choosing an engineering partner with proven international regulatory expertise is critical to speed-to-market and long-term ROI.

Product Applications

Where Our Products Are Used

  • 1

    IV Infusion Production Lines

    Complete systems for Non-PVC soft bag, PP bottle, and glass bottle IV solutions, from compounding to filling and sterilization.
  • 2

    Ampoule & Vial Filling Lines

    High-speed aseptic filling and sealing lines for injectable formulations, fully compliant with cGMP requirements.
  • 3

    Oral Solid Dosage (OSD) Plants

    Integrated granulation, tablet pressing, capsule filling, coating, and blister packaging for tablets and capsules.
  • 4

    Pharmaceutical Water Treatment Systems

    Purified water (PW) and water for injection (WFI) generation, storage, and distribution systems meeting pharmacopeia standards.
  • 5

    Cleanroom & HVAC Engineering

    Full facility design including classified cleanrooms, HVAC zoning, and environmental monitoring systems.

technology

Pain Points & Solutions

  • Pain Point: Navigating multi-standard GMP compliance (EU, FDA, WHO) across different export markets is complex and costly.

    Solution: IVEN engineers every project to meet EU GMP, US FDA cGMP, WHO GMP, and PIC/S GMP simultaneously — one build, multiple certifications.

  • Pain Point: Coordinating dozens of equipment vendors leads to integration failures and project delays.

    Solution: Single-source turnkey delivery — from facility design and equipment manufacturing to installation, commissioning, and validation under one contract.

  • Pain Point: Lack of post-installation support causes extended downtime and failed audits.

    Solution: Lifetime after-sales service including spare parts supply, remote diagnostics, on-site maintenance, and revalidation support.

  • Pain Point: Scaling production while maintaining quality consistency is a persistent challenge.

    Solution: Fully automated production lines with in-line quality monitoring, reducing human error and ensuring batch-to-batch consistency.

Advantages

Why Choose Us

  • 20+ years of specialized pharmaceutical engineering experience

  • 4 dedicated manufacturing facilities ensuring quality control and delivery speed

  • 40+ turnkey projects delivered across 70+ countries on 5 continents

  • Multi-standard GMP compliance — EU GMP, FDA cGMP, WHO GMP, PIC/S built into every project

  • Full lifecycle service — consulting, design, manufacturing, installation, validation, training, and lifetime support

  • Proven regulatory track record — facilities engineered by IVEN have passed inspections by EU, FDA, and WHO auditors

case

Success Snapshot

  • Leading Pharmaceutical Group

    Southeast Asia

    Delivered a complete IV soft bag infusion plant with an annual capacity of 100 million bags. The facility passed WHO GMP pre-qualification on the first inspection, enabling the client to supply national tenders within 14 months of project kickoff.

  • Major Generics Manufacturer

    Africa

    Provided a full OSD turnkey plant covering tablets and capsules. Production efficiency increased by 60% compared to the client’s legacy facility, achieving EU GMP certification and opening access to regulated export markets.

testimony

Trusted by Industry Leaders

  • “IVEN handled everything from cleanroom design to production line validation. We passed our WHO audit on the first attempt — that speaks for itself.”

    Mr. K

    Plant Director

  • “What impressed us most was the seamless integration. One partner, one timeline, zero finger-pointing between vendors. Our line was operational 2 months ahead of schedule.”

    Ms. R

    VP of Operations

Support

FAQ

All systems are engineered to meet EU GMP, US FDA cGMP, WHO GMP, and PIC/S GMP standards simultaneously.

Yes. We deliver full turnkey projects — from feasibility study and facility design to equipment supply, installation, validation, and operator training.

Depending on scale and complexity, most projects are completed within 12–18 months from contract signing to commercial production.

Absolutely. We offer lifetime global after-sales service including on-site engineers, remote support, spare parts, and revalidation assistance in 70+ countries.

Yes. We provide retrofit and expansion solutions for existing plants, upgrading equipment and facilities to meet current GMP standards.

Related Industry Solutions

  • End-to-End GMP Manufacturing Solutions for Oncology Drug Production

    From injectable chemotherapy filling lines to oral solid dosage systems and turnkey oncology facilities — purpose-built infrastructure to bring cancer therapies to market faster.

  • GMP-Compliant Production Systems for Vaccine Fill-Finish & Biomanufacturing

    From vial and ampoule filling lines to bioreactors, cleanrooms, and water systems — integrated vaccine manufacturing infrastructure engineered for global regulatory approval.

  • Pharmaceutical Water Purification Systems & Cleanroom Engineering Solutions

    GMP-compliant PW, WFI, and clean steam generation systems paired with ISO-classified cleanroom design — the critical utility backbone for every pharma manufacturing facility.

  • Integrated Bioprocessing Systems & Turnkey Biopharmaceutical Factory Solutions

    From bioreactors and aseptic filling lines to cleanroom and water systems — complete GMP-compliant manufacturing infrastructure for biologics producers worldwide.

  • Turnkey Injectable & IV Solution Production Lines — From Design to GMP Delivery

    Integrated manufacturing systems built to EU GMP, US FDA cGMP, WHO & PIC/S standards — trusted by pharmaceutical producers in 60+ countries.

  • Automated Production Lines for Medical Devices & Consumables Manufacturing

    High-speed assembly systems for blood collection tubes, syringes, blood bags, and needles — engineered to international quality standards and delivered turnkey worldwide.

  • Automated Production Lines for Blood Bags, Collection Tubes & Transfusion Devices

    GMP-compliant, fully integrated manufacturing systems for blood banking consumables — from blood bag making to vacuum tube assembly and collection needle production.

  • Complete GMP Production Lines for Oral Solid Dosage Manufacturing

    From granulation and tableting to coating, capsule filling, and packaging — turnkey OSD plant solutions engineered for global regulatory approval.