Actiza Pharmaceutical Pvt. Ltd. is emerging as a leader in pharmaceutical manufacturing, exporting, and supplying from India.
“Innovate and automate, with human touch in manufacturing process to provide affordable pharmaceutical products to make a healthier world.”
Actiza Pharmaceutical Pvt. Ltd. follows high global standards in formulation manufacturing with latest machinery. We are specialized in the manufacturing and exporting of finished formulations that cater to the most demanding global needs. We are on the verge of becoming one of the largest pharmaceutical companies in India when it comes to contract manufacturing of Tablets, Capsules, Injections,Creams/Ointments, Drops, Infusion, Inhaler, Lotion, Gel, Suspension / syrup, Nasal Drops/Sprays, etc.
The manufacturing and R&D facility of Actiza Pharmaceutical Pvt. Ltd. is located in Surat, Gujarat, India. It contains multiple formulation facilities in close proximity that are further sub-divided to specific zones dedicated to particular tasks. With well-established supply chain and vendor development systems, we have built an in-house pharmaceutical ecosystem.
Our world-class manufacturing plant is equipped with modern high-speed machines and integrated packaging lines. Our heavily automated systems include non-fill devices, collators, multi-station tablet presses, brevetti visual inspection machines, FFS machines and high-speed vial/ampoule filler/sealer. Our Highly professional research team works hand-in-hand with the machines to manufacture high-quality cost-efficient products.
To support our end-to-end pharmaceutical capabilities, Actiza Industry operates as a wholly owned subsidiary of Actiza Pharmaceutical Pvt. Ltd., specializing in the manufacturing of Active Pharmaceutical Ingredients (APIs) and pharmaceutical intermediates. This backward integration enhances our ability to maintain strict quality control, optimize supply chains, and ensure regulatory compliance across all markets. As a reliable API manufacturer, Actiza Industry plays a critical role in delivering high-quality raw materials that power our finished formulations, reinforcing our commitment to excellence from molecule to medicine.
From dossier preparation to marketing authorization filing, our Pharmaceutical Regulatory Services cover CTD, eCTD, and ACTD formats supporting product registration across 40+ countries in both regulated and semi-regulated markets.
These are Some of the Key Features of Our Pharmaceutical Manufacturing Plant:
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The continuous and uninterrupted flow of Process & Facilities that comply with Schedule “M” Specifications & WHO-GMP norms.
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Effective sanitation and fully automated HVAC System.
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Facility to manufacture every variety of tablets including un-coated, film-coated, double-layered, sugar-coated, enteric coated and slow release tablets.
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VAHP chillers that are 100% environment friendly.
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Duo Pass Reverse Osmosis water system/ de-mineralization plant.
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Multi-Stage Distillation plant.
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De-Humidification unit and dust extraction systems and separate AHUs for each zone.
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Zone-wise segregation of every critical processing activity, to prevent cross-contamination
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Even uniforms are marked with zone-specific colors to ensure complete segregation.
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Isolated and dedicated facilities for producing B-Lactam and Cephalosporin dosage forms.
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Area-specific Air Environment Conditioning with respect to temperature, pressure, humidity, filtration, etc.
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Zero-discharge Effluent Treatment Plant.
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Alternative power generation system to ensure uninterrupted production and Separate air handling units for each production department.
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In house R&D facility with experienced and talented researchers.
All the above-mentioned facilities are WHO, GMP certified and ISO 9001 accredited for systems. Regular global audits are conducted to further uplift our standards.
As a result, we have grown into leading pharmaceutical drug manufacturers over the years. With the goodwill and trust of our customers, the best is yet to come!
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