Pharmaceutical

We Serialise, Resource and Optimise Packaging Lines for Compliance, Operational Efficiency and Speed to Market 

The manufacturing and packaging of pharmaceutical product is highly regulated. At CXV Global, we have a deep understanding of the processes and challenges occurring in the industry. For over 30 years, CXV Global have been assisting pharmaceutical manufacturers who face significant challenges in advancing product quality and still meeting the demands of growing the bottom line and overall business profitability. A case in point is our innovative 360 Degree Bottle and Vial Inspection System specifically designed for the pharmaceutical industry.

CXV Global is an ideal partner to help pharmaceutical manufacturers design and develop products that meet industry connectivity and interoperability requirements and standards. Our solutions and services are geared towards reducing development costs, improving time to market, and reducing the barriers to market entry.

Helping You Achieve Maximum Patient Safety

Our solutions comprise of machine vision inspection, vial and blister inspection, vial counting, robotics, serialisation, line clearance assistance, digitalisation and resourcing. Our solutions provide compliance with industry regulations including the Falsified Medicines Directive, FDA CFR 21 Part 11 and GAMP standards.

CXV Global has played a key role in helping our clients succeed in all aspects of the Pharmaceutical Industry from Drug Discovery and Research & Development to Pre-Clinical & Clinical Operations to Automated Manufacturing and Packaging / Supply Chain, including Regulatory and GXP Compliance.

CXV Global Value Chain
Drug Development Lifecycle

Discovery

  • End-to-End System, Data & Process Integration
  • Total Laboratory Automation
  • Laboratory Informatics
  • Web Based Materials Management System

Development

  • Laboratory Informatics
  • Laboratory Automation
  • GxP Compliance

Clinical Trials

  • Clinical Trials Data Management
  • Clinical Supply Chain
  • GxP Regulatory Compliance
  • GxP Computer Systems Validation

Manufacturing

  • Manufacturing Process Automation
  • Automation Layer Data Aggregation
  • Process Control
  • Automation
  • Supervisory Control Data Acquisition
    (SCADA)
  • Manufacturing Informatics
  • GxP Computer Systems & Equipment
    Validation

Packaging

  • Machine Vision Systems
  • Robotics
  • SCADA
  • Manufacturing Informatics
  • Total Packaging Line Automation
  • GxP Computer Systems & Equipment Validation
  • Warehouse Management Systems (WMS)
    Serialization Returns & Verification
  • Warehouse Performance Monitoring / Energy
    Usage E Commerce Fulfilment Solutions
  • Automated Sorting
  • Automated Storage and Retrieval Systems (ASRS)
  • Location Monitoring (GPS Enabled RFID Tags)
  • Supply Chain Security – Serialization – DSCSA
    Solutions
  • Machine Vision & RFID Systems
  • Robotics
  • GxP Computer Systems & Equipment Validation

Automate & Improve the Inspection of Pharmaceutical Products & Packaging 

CXV Global automate many inspection and automation functions around your sterile fill-finish and oral solid dose manufacturing and packaging operations.

The inspection of pharmaceutical products and packaging to ensure patient safety is a critical quality control function. Machine vision technology delivers standards of resolution, speed and repeatability not possible with manual visual inspection. 

Digitalising The Line Clearance Process

Using patent pending technology to reduce line changeover times is the single greatest potential for improving line availability: entire shifts worth of availability can be unlocked by deploying a machine vision system that conducts inspections in milliseconds that would normally take operators minutes.

The CXV Global SmartFactory LineClearance Assistant (LCA) is a machine vision system which assesses the line clearance during line changeovers through objective electronic decisions that are quicker to achieve and repeatable when compared with manual line clearance procedures.

 

Resourcing Models Designed Around Your Needs

 

Project Resourcing 

CXV Global provides a specific engineering resource, or alternatively, a cross-functional engineering team.

Managed Service Provision
Insource CXV Global expertise to take responsibility for productivity, compliance and quality while operating under client SOPs, KPIs and final approval. The client has visibility and control as CXV Global staff carry out the work.

Functional Service Provision
CXV Global manage the delivery of a function to the pharmaceutical manufacturer customer using CXV Global people to deliver and manage the agreed customers goals. You the customer own the assets  – CXV Global fully manages them for you.

Regulation

The pharmaceutical industry is secured globally through a complex network of regulations. From research and patent applications to packaging and prescribing, each stage in a drug’s life cycle requires compliance with an associated regulation. We support compliance with constantly evolving regulations, from GAMP to anti-counterfeiting.

How can we help?

We’ve been leading the way in the solutions we bring to customer problems and in the deployment of leading edge technologies for over 30 years.

We are proud of our long-term customer relationships, where knowledge, experience and trust come together to forge strong partnerships.

Upcoming Pharma Events 
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