Pharmaceutical Manufacturing & CDMO Automation

Precision-engineered systems to optimize production, ensure compliance, and reduce downtime.

Automation Solutions for Pharma and CDMO Production Lines

FP Developments partners with pharmaceutical manufacturers and CDMOs to deliver advanced automation systems for filling, labeling, and packaging operations.

Our equipment is designed for scalability, data integrity, and long-term reliability across aseptic and non-aseptic processes. From small-batch R&D to full production lines, we help contract manufacturers achieve consistent quality and compliance with every run.

With over 60 years of engineering experience, we understand the operational challenges of pharma production—and we build systems that improve efficiency, traceability, and throughput without compromising safety.

Pharma Manufacturing Service, Support, Parts & Material Handling

With over 50 years as an American OEM for the pharmaceutical industry, we aim to fill the service gap by supporting our own equipment as well as other brands. We provide preventative maintenance, emergency service, internal maintenance support, upgrades and alterations as well as custom solutions to difficult engineering problems.

Label Removal

We offer purchase, leasing, on-premises removal, and buyback options of the HURST Corporation Label Stripper.

Automated Syringe Filling Pump

Our Rotary Model pump delivers a streamlined path to USP compliance while strengthening sterility assurance.

F.P. Equipment Support

We provide preventative maintenance, emergency service, maintenance support, upgrades and more.

Some Frequently Asked Questions

A CDMO (Contract Development and Manufacturing Organization) provides outsourced services for drug development, formulation, scale-up, and commercial production for pharmaceutical companies.

While CMOs focus primarily on manufacturing, CDMOs handle both development and production — supporting formulation optimization, analytical method development, and regulatory submission support

The FDA (U.S.), EMA (Europe), and MHRA (U.K.) regulate manufacturing under cGMP requirements to ensure quality, safety, and traceability across all production stages.

Key trends include continuous manufacturing, single-use bioprocessing, serialization, and automation to improve quality and efficiency.

It involves transferring validated manufacturing processes, analytical methods, and quality documentation under strict data and IP controls to ensure reproducible performance at scale.

Capacity constraints, complex biologic formulations, and increasing regulatory scrutiny. Many CDMOs are investing in digital quality management systems and flexible aseptic fill-finish lines.

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Contact FP Developments

Ready to enhance your production capabilities with precision and innovation? Whether you’re looking to optimize an existing line, implement cutting-edge automation, or develop a custom solution, FP Developments Inc. is here to help. With over 60 years of expertise in pharmaceutical, biotech, and medical device packaging and machinery, we deliver solutions that meet your unique challenges.

Get in Touch Today

Connect with us to learn more about how we can support your business:

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Our team is ready to answer your questions, offer insights, and provide tailored solutions to meet your manufacturing and compliance needs.

Let’s create a solution that works for you—today and tomorrow.

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