Infrastructure & Facilities

Our Advanced Packaging Infrastructure

Right Angle Pharmapack is a premier pharmaceutical packaging specialist committed to excellence and regulatory compliance. We manufacture high-precision caps, closures, measuring cups and other primary packaging components in a fully controlled, classified production environment tailored to pharma norms.

Our operations are backed by prestigious certifications: a US DMF Type III registration, ensuring our product dossiers meet stringent U.S. drug master file standards; and accreditation by TÜV SÜD for ISO 9001 quality-management systems along with GMP compliance, reinforcing our dedication to consistent process control, traceability and product integrity. With this certification trifecta, Right Angle Pharmapack assures customers of world-class manufacturing practices, robust documentation and readiness to serve regulated markets with confidence and reliability.

High-Precision Moulding Facility

At Right Angle Pharmapack we deploy high-precision injection-moulding capabilities using the world-class machines from Milacron, ensuring best-in-class quality and consistency for our pharmaceutical packaging components. Production takes place entirely within our classified clean-room zones which are designed to meet rigorous pharma-industry norms for cleanliness, contamination control and process traceability.

We maintain strict environmental controls, validated work flows and hygiene protocols to uphold regulatory compliance. Our integrated manufacturing environment allows us to mould critical packaging components in-house — from raw resin handling to the final inspection — thereby reducing external dependencies, shortening lead-times and enhancing quality oversight. With Milacron’s state-of-the-art injection platforms and our dedicated classified production area, Right Angle Pharmapack delivers robust packaging solutions that meet the demanding standards of the pharmaceutical sector while ensuring operational excellence, regulatory readiness and a premium outcome for our customers.

Customized Packaging & Cap Assembly

Our in-house child-resistant cap (CRC) assembly machine is engineered to deliver high-precision, clean, and reliable performance tailored for pharmaceutical packaging. Built with industrial-grade stainless steel frames and enclosed hygienic modules, the system integrates automated cap feeding, liner insertion and cap locking mechanisms to accommodate our full range of PP child-resistant caps (20 mm–53 mm diameter).

The feeder bowl orients caps and feeds them into an assembly station where the machine inserts seal-liners and then completes the push-down-and-turn or squeeze-and-turn locking action that defines child-resistant closures. Sensors monitor each cycle to detect misfeeds, missing liners or mis-assembled caps, rejecting non-conforming units in real time. The machine supports adjustable settings for torque, dwell time and cap height, enabling quick change-overs between sizes and variants. Designed for full integration into our capping line, the system ensures secure closure while maintaining throughput and hygiene demands of pharmaceutical primary packaging. With our in-house assembly capability, Right Angle Pharmapack ensures strict quality control, traceability of each cap batch and regulatory compliance—with minimal external dependencies.

Rigorous In-Process Inspection Setup

At Right Angle Pharmapack, our designated Quality Assurance (QA) team undertakes rigorous inspections of every cap and measuring cup produced, ensuring absolute adherence to pharmaceutical industry standards. From the moment components emerge from our injection-moulding lines, the QA team undertakes detailed visual checks to identify surface defects, dimensional inconsistencies and any signs of contamination — in line with accepted packaging inspection protocols.

• Micro-processor machine controls for dimensional accuracy.
• Automated torque and dwell-time sensing controls.
• Cleanroom environmental validation logs recorded per shift.

Final QA Release Testing & Dispatch

Before any batch is released, each cap and cup batch undergoes final QA release testing. Records capture batch numbers, inspection outcomes, deviations, and corrective-action details, ensuring full traceability. This diligence guarantees that our closures and dosing cups not only meet specified tolerances and functional requirements but also maintain the hygiene, safety and quality standards critical for pharmaceutical packaging.

All finished products are double-bagged in food-grade liners inside heavy-duty corrugated shippers, labeled with batch details, and stored in a temperature-controlled dust-free storage area prior to secure shipment in clean, sanitized transit vehicles.