Insights, News, and Answers

Pharma Packaging Systems Resources Hub

Here you’ll find the latest company updates, product developments, and useful information to help you get the most from our packaging solutions.

Updates from PPS

Latest News & Industry Insights

Stay up to date with the latest company news, industry developments, and expert insights from our team. 

Frequently Asked Questions

Our FAQs cover the most frequently asked questions about our systems and services. If you can’t find what you’re looking for, our technical team is always ready to help.

What types of machines do you offer?

We design and manufacture electronic counting systems for tablets and gel capsules, available as stand-alone units or fully integrated into complete packaging lines.

Are your systems cGMP compliant and FDA-ready?

Yes. All equipment complies with current Good Manufacturing Practices and, where applicable, supports 21 CFR Part 11. Documentation includes manuals, certifications, and IQ/OQ validation packages.

Can your counting machines integrate with existing packaging lines?

Yes. Our systems are modular and can be integrated into existing lines or operate independently, depending on your requirements.

What throughput do your counting systems offer?

Performance depends on model configuration. Our high-speed Pharmacount range is built for high-volume tablet and capsule applications.

What support and training do you provide?

We offer full lifecycle support: on-site training, remote assistance, service visits, and spare parts. Validation documentation and operator training can be included with each purchase.

How adaptable are your machines for different product types?

Our systems can handle a wide range of solid dose products including tablets, capsules, soft gels, gummies, dishwasher pods, chocolate wafers, and even hardware components. Format parts are adjustable for product size, shape, and material.

Do you offer customisation for specific needs?

Yes. We can customise both hardware and software to meet your product characteristics, regulatory environment, and facility layout.

What’s included in the IQ/OQ documentation?

Each system includes an optional validation package with Installation Qualification (IQ), Operational Qualification (OQ), test reports, and traceable records suitable for regulatory submission.

How do we start the procurement process?

Contact our sales team via phone, email, or the online enquiry form. We’ll assess your production needs, recommend suitable equipment, and coordinate pricing, demonstrations, and lead times.

Can we see the equipment before buying?

Yes. You're welcome to visit our UK site in Pershore to see the machines in operation. We also offer virtual demos or visits to existing customer installations, subject to availability.

Downloads

Brochures, Datasheets & Technical Documentation

Access our latest product literature, specifications, and validation documents — available on request.

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