Facilities
Manufacturing Facilities
We operate two manufacturing units strategically located in Tamil Nadu. Unit I, based in Mangadu, Chennai, and Unit II, located in Thiruvallur, approximately 40 km from Chennai, are both equipped with advanced cGMP-compliant manufacturing facilities.
Specializing in third-party manufacturing, we produce a wide range of pharmaceutical finished products. Our product portfolio includes Pharmaceuticals, Nutraceuticals, and Food Supplements, available in various dosage forms such as tablets, capsules, powders for oral suspension, and liquids.
Unit I, located in Mangadu, Chennai, is GMP-compliant and has been operational since its approval in 2007. Unit II, established in 2024 in Thiruvallur (approximately 40 km from Chennai), is also GMP-compliant and adheres to the more stringent Revised Schedule M guidelines set by the Indian Government.
We are committed to enhancing our manufacturing standards and are planning to pursue WHO-cGMP certification for Unit II in the future to align with global benchmarks.


Key Features
Total Site Area: Approximately 2.15 acres.
Total Plinth Area: Around 25,600 sq. ft..
Dedicated QC Laboratory: A state-of-the-art facility spanning 3,500 sq. ft., equipped with the latest sophisticated instruments adhering to GLP norms.
Advanced Manufacturing Equipment: Outfitted with the latest cGMP-compliant machinery, ensuring adherence to current Good Manufacturing Practices.
Unit II Compliance: Our new Unit II is approved as per Revised Schedule M, reflecting our commitment to stringent manufacturing standards. We are actively working towards obtaining WHO-cGMP certification to meet international quality benchmarks.
Mechanized Handling Systems: Designed in accordance with international quality standards, our mechanized handling systems enhance efficiency and maintain product integrity.
Comprehensive HVAC System: Fully equipped with a robust Heating, Ventilation, and Air Conditioning (HVAC) System, ensuring optimal environmental conditions throughout the facility.
Environmental Monitoring and Validation: Implementing a rigorous environmental monitoring, calibration, and validation program to maintain a flawless production environment.
Expertise in Solid Oral Dosage Forms: Well-established capabilities in the development and commercialization of solid oral dosage formulations, including tablets, capsules, powders for oral suspension, and liquids.
Quality Assurance
Our Quality Assurance (QA) Department is equipped with state-of-the-art instruments, including High-Performance Liquid Chromatography (HPLC) systems, ensuring the production of top-tier pharmaceutical products in strict adherence to regulatory guidelines.
We implement rigorous quality control procedures at every stage, beginning with source validation, sampling, and analysis of raw materials, and extending through to meticulous documentation and the release of finished products.
A comprehensive Quality Management System (QMS) is integral to our operations, with all manufacturing processes and analytical methods fully validated.
Our team is dedicated to embracing the latest technologies for continuous improvement, recognizing that quality is an ongoing journey rather than a finite goal.
This commitment ensures that our products consistently meet the highest standards of safety and efficacy.
Research and Development
We are in the process of establishing a dedicated Research and Development (R&D) Division to drive innovation and enhance our product offerings. This strategic initiative underscores our commitment to advancing pharmaceutical research and delivering high-quality, effective solutions to meet the evolving needs of healthcare.
Environental Sustainability
At AASSK Pharmaceuticals, we prioritize environmental sustainability by closely monitoring our production lines to ensure that our operations and by-products do not harm the ecosystem.
Our facilities are designed to manage waste effectively and minimize pollution.
We utilize an Effluent Treatment Plant (ETP) to treat wastewater, ensuring that harmful substances are removed before discharge, thereby protecting aquatic life and public health.
Maintaining environmental cleanliness and safety is among our top priorities.
Our commitment to environmental sustainability is reflected in our continuous efforts to adopt and implement eco-friendly practices across all operations.