Manufacturing Services

Manufacturing Services

Pagari Pharma is client First CDMO believes in quality product at affordable price from concept to commercialization with state of art Tablet Compression Machine, Encapsulation Machine, and Bottle filling Packaging line.

Over The Counter (OTC) Solid Oral Dosage Form (Tablets And Capsules)

Liquid capability (Small Scale up to 200 Liter)

Bottle Filling Tablets And Capsules

Prescription (Rx) Solid Oral Dosage Form (Tablets and Capsules)

Pharmaceutical Manufacturing Equipment

01

Weighing Balance

At our facility, the Weighing Balance is one of the most essential tools, ensuring precision and consistency in every batch we produce. It is used to measure raw materials, active ingredients, and excipients with high accuracy—often down to the milligram level—crucial for maintaining formulation integrity and meeting regulatory compliance.

Our balances are regularly calibrated and validated to comply with USP <41> and <1251> standards for repeatability and accuracy.

02

Sifter

At our facility, the Sifter plays a vital role in ensuring consistent particle size and quality of raw materials used during formulation. It is primarily used to separate particles based o nthe size before they proceed to mixing or granulation. This helps maintaining uniformity and flowability—both critical for accurate dosing and tablet/capsule consistency.

Our sifter is made of high-grade stainless steel and designed to meet stringent cGMP and hygiene standards. It features interchangeable sieves, allowing us to adapt to different product requirements with ease. The equipment’s easy dismantling and cleaning reduce downtime and ensure minimal cross-contamination risk.

03

V-blender

Our facility is equipped with 20 Cu. ft. V-blenders to support Large Scale production. The V-blender is essential for achieving a homogenous mixture of powders and granules, which is critical for uniform drug content in each dose. Its gentle tumbling action is ideal for heat-sensitive or fragile materials. The unit is designed with stainless steel contact parts and easy-clean access for batch-to-batch changeovers.
04

Lab Washer

Our Lab Washer is a vital part of maintaining cleanliness and compliance across cGMP manufacturing facility. Designed for efficient cleaning of glassware, stainless steel tools, and lab instruments, it ensures consistent and validated cleaning cycles that meet stringent pharmaceutical Cleaning Validation standards.

Equipped with programmable wash cycles, HEPA filtration, and drying capabilities, our lab washer minimizes the risk of cross-contamination and reduces manual handling errors. It supports both high-throughput and delicated lab operations by providing repeatable, validated cleaning performance. All cleaning processes are thoroughly documented, supporting traceability for audits and regulatory inspections. This system plays a key role in maintaining a sterile environment, ultimately contributing to the accuracy and reliability of our lab results.

05

Tablet Press

Our facility features a state of art new Tablet press with high-output rotary presses like the 39-Station D and 45-Station B turret systems for commercial manufacturing. These machines are essential for producing uniform tablets with consistent weight, hardness, Friability, and disintegration profiles. Located in our Texas cGMP facility, Tablet press is housed in ISO-classified cleanrooms and maintained under strict preventive maintenance programs. They comply with 21 CFR Part 11 requirements for electronic batch records. Whether for pilot batches or full-scale runs, our tablet compression equipment ensures quality, compliance, and performance.
06

Encapsulation Machine

Our encapsulation machine supports production-scale capsule filling, with a capacity of up to 90,000 capsules per hour. This high-efficiency equipment enables precise dosing of powders, pellets, or granules into hard gelatin or HPMC capsules. Used extensively in both clinical development and commercial manufacturing, the system ensures consistent fill weight and low rejection rates. Its modular design allows rapid format changes between capsule sizes, making it ideal for flexible batch requirements. The unit is equipped with in-line sensors for real-time fill monitoring and rejection of underfilled capsules. This machine plays a critical role in solid oral dosage manufacturing, providing scalability, accuracy, and speed—all with a focus on regulatory compliance and patient safety.
07

200 L Jacketed Vessels

Our 200 L Jacketed Vessels are essential for batch processing under controlled temperature conditions. Designed for use in cGMP manufacturing, they support mixing, heating, and cooling of pharmaceutical liquids while maintaining process integrity and uniformity.

The Overhead Mechanical Shaker facilitates consistent agitation and ensure homogenity.

An equipment is maintained per cGMP and validated to meet pharmaceutical regulatory standards at our newly built facility.

07

Air Compressor

Our pharmaceutical-grade air compressor provides a reliable source of clean, compressed air required for various equipment operations and pneumatic controls across R&D, cGMP manufacturing, and laboratory areas. Designed for continuous duty, it ensures consistent airflow and pressure stability, critical for maintaining process accuracy.

Equipped with oil-free technology, the compressor helps eliminate the risk of product contamination—meeting the stringent air quality standards required in regulated pharmaceutical environments. It supports key processes such as capsule filling, fluid bed drying, and granulation where clean compressed air is essential.

Integrated filtration systems and dryers ensure the output air is free from moisture, oil, and particulates. Regular validation and maintenance are performed in line with cGMP protocols to ensure operational safety and compliance.

The air compressor serves as the backbone of many automated systems, providing clean, pressurized air that supports efficiency, hygiene, and regulatory adherence across our Texas-based facility.

08

Purified Water System

Our Purified Water System is a critical utility in both R&D and cGMP manufacturing areas, designed to produce high-quality water that meets USP and EP standards. It employs multi-stage purification—typically involving reverse osmosis, deionization, and UV treatment—to ensure the removal of organic and inorganic contaminants, bacteria, and endotoxins. This validated system supports formulation, equipment cleaning, and analytical processes, helping maintain product integrity and regulatory compliance. With continuous monitoring and 21 CFR Part 11-compliant data logging, it ensures consistent water quality for pharmaceutical applications. Installed in our Texas-based facility, the system is maintained under strict cGMP protocols, supporting reproducible results and minimizing contamination risks.
09

Stability Chamber

Our Stability Chamber plays a vital role in conducting accelerated and long-term stability studies for pharmaceutical products. It is designed to simulate various environmental conditions such as temperature, humidity, and light, enabling us to evaluate the shelf life and performance of drugs under controlled settings. Equipped with precise temperature and humidity control, our chamber supports ICH guidelines (Q1A) and ensures consistent conditions throughout the testing period. The chamber includes features like uniform airflow, automatic alarms, and data logging capabilities for comprehensive monitoring and compliance documentation. We use the Stability Chamber for storing samples during real-time and accelerated testing phases, helping us generate reliable data required for regulatory submissions. Its performance supports our commitment to developing high-quality, stable pharmaceutical formulations. Our Texas-based facility uses validated, 21 CFR Part 11-compliant stability chambers, monitored continuously to maintain integrity. They play a crucial role in quality assurance, ensuring products remain effective and safe throughout their intended lifecycle.
10

Bio Safety Cabinets

Our ISO Class 5 biosafety cabinets ensure aseptic sample handling in a sterile, HEPA-filtered airflow environment. They are used during microbiological testing, sample preparation, and dispensing of potent or sensitive APIs. Each cabinet includes UV sterilization, airflow monitoring, and safety interlocks to protect both product and personnel. Located in controlled areas of our Texas facility, these cabinets support sterile applications, including endotoxin testing and environmental monitoring. Their use is critical in preventing cross-contamination and maintaining cGMP-compliant handling procedures.