Pharma
Pharma machinery solutions support the full spectrum of aseptic pharmaceutical manufacturing, from pharma processing, precise filling to safe transfer and quality control. Designed around advanced isolation technology, they create controlled, contamination-free environments that protect both operators and products. Fully GMP-compliant, these systems ensure reliability and safety in applications such as injectables, vaccines, and high-potency compounds, playing an important role in driving the advancement of Pharma 4.0.
Pharma Isolator
Function and Purpose
A pharmaceutical isolator is a fully enclosed, gas-tight, and sterile system that provides a physical barrier to ensure contamination control and operator protection.
Depending on process requirements, isolators can operate under:
- Positive pressure for product protection
- Negative pressure for product & operator safety
They are essential for aseptic compounding, fill-finish operations, and handling of potent compounds.
Tailin Isolator Portfolio
Tailin provides customized isolation systems that comply with GMP, USP, and EP standards, including:
- Sterility Test Isolators
- Aseptic Filling Isolators
- Containment Isolators for APIs and HPAPIs
These systems effectively reduce contamination risks and ensure consistent, reliable performance in drug production.
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Pharmaceutical Dispensing
Precision and Automation
Tailin High-Precision Pharmaceutical Dispensing Solutions enable automated aseptic filling, capping, and stopper operations for R&D, trial and pilot-scale production.
They ensure GMP compliance, and deliver precise, zero-waste performance to accelerate lab-to-clinic development.
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Sterile Transfer
Safe and Contamination-
Free Transfer
Sterile Transfer ensures materials or products move safely between cleanrooms or controlled environments. It maintains aseptic conditions, prevents cross-contamination, and ensures compliance with GMP standards in pharmaceutical operations.
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Integrity Testing
Glove Integrity Testing
In aseptic production, isolators and RABS systems require regular integrity verification to maintain sterility.
For isolators, leak testing of the glove system should be performed using a methodology demonstrated to be suitable for the task and criticality.
For RABS, gloves should be visually examined with each use, and integrity testing should be performed at periodic intervals.
Filter Integrity Testing
Sterilizing-grade filters are essential barriers ensuring product sterility. Integrity testing verifies
filter performance, confirming compliance with global GMP requirements.
Tailin Filter Integrity Testers offer multiple standard functions:
Forward Flow Test
Bubble Point Test
Water Intrusion Test
Combined Forward Flow and Bubble Point Test
Pressure Hold Test
Container Closure Integrity Testing (CCIT)
Container closure integrity (CCI) refers to the ability of a pharmaceutical packaging system to prevent product loss, microbial ingress, and the entry of other gases. For sterile products, a robust packaging system is essential to ensure product safety and quality.
Typical testing methods include:
- Vacuum/Pressure Decay
- High-Voltage Leak Detection
- Headspace Analysis
- Microbial Challenge Testing
Tailin Container Closure Integrity Tester (CCIT) is a high-precision leak testing solution specifically designed for the pharmaceutical and biopharmaceutical industries, providing reliable and compliant verification of packaging integrity.
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