Time Pharmaceuticals

Production Units & Capabilities

The Production Department operates in strict compliance with established quality and regulatory standards, ensuring that all products consistently meet global benchmarks. Designed with efficient spatial configurations and equipped with state-of-the-art technology, the facility supports high-throughput manufacturing across multiple dosage forms to address evolving market needs.

The department maintains close integration with the R&D division to enable the seamless transfer of technology and the commercialization of innovative, safe, and efficacious pharmaceutical products. A team of highly skilled professionals, supported by robust quality systems and a culture of continuous process improvement, drives operational excellence and manufacturing efficiency.

Dosage Capabilities:

The production facility is equipped to manufacture a diverse range of pharmaceutical dosage forms, including Tablets, Capsules, Oral Liquids (Syrups/Suspensions), and Topical Preparations (Ointments/Creams).

Infrastructure & Equipment:

State-of-the-art, high-efficiency manufacturing equipment enables scalable production while ensuring consistency, precision, and minimal product variability across all dosage forms.

Quality & Compliance:

All operations are conducted in full adherence to current Good Manufacturing Practices (cGMP) and WHO GMP guidelines, ensuring regulatory compliance and the highest standards of product quality, safety, and efficacy.

Penicillin Manufacturing Unit

A dedicated, standalone facility established in 2063 B.S., the Penicillin Unit is designed to handle β-lactam antibiotics with complete containment and compliance.

Dosage Forms Handled:

• Tablets
• Capsules
• Powder for Oral Suspension

Facility Highlights:

• Operates as an independent block to ensure complete segregation from non-β-lactam production areas.
• Implements validated cleaning protocols, dedicated HVAC systems, and unidirectional personnel and material flow to guarantee zero cross-contamination.
• Adheres strictly to cGMP and WHO GMP standards to ensure product safety, efficacy, and regulatory compliance.

Cephalosporin Manufacturing Unit

A purpose-built, dedicated facility commissioned in 2072 B.S., the Cephalosporin Unit is engineered to handle cephalosporin-class antibiotics with the highest standards of containment and compliance.

Dosage Forms Manufactured:

• Tablets
• Capsules
• Powder for Oral Suspension

Facility Features:

• Utilizes closed processing systems and dedicated equipment to ensure product integrity and operator safety.
• Equipped with independent Air Handling Units (AHUs) for each operational area to prevent cross-contamination and maintain classified cleanroom environments.
• Designed with stringent contamination control measures, including pressure differentials, validated cleaning procedures, and restricted access protocols, in full alignment with cGMP and WHO GMP guidelines.

Sterile Manufacturing Unit

Commissioned in 2067 B.S., the Sterile Unit is a dedicated facility designed specifically for the aseptic manufacturing of sterile pharmaceutical products, ensuring the highest levels of product safety and compliance.

Dosage Forms Produced:

• Eye Drops
• Ear Drops
• Nasal Drops

Facility Highlights:

• Operates under validated aseptic processes in classified cleanroom environments, supported by Laminar Air Flow (LAF) systems, HEPA filtration, and pressure cascade controls.
• Utilizes high-purity raw materials and sterile-grade excipients, sourced and handled under strict quality standards.
• Comprehensive quality control and in-process monitoring ensures microbial and particulate control in accordance with cGMP, WHO GMP, and pharmacopeial guidelines (IP, BP, USP).
• All equipment, utilities (HVAC, compressed air), and personnel undergo regular validation and training to maintain sterility assurance levels (SAL).

Non-Penicillin Manufacturing Unit

The Non-Penicillin Section at TIME Pharmaceuticals Limited is a fully segregated, WHO-GMP–compliant facility designed to ensure zero cross-contamination with Penicillin products. Equipped with dedicated HVAC systems, modern production lines, and validated cleaning protocols, we manufacture tablets, capsules, ointments, creams, and oral liquids across a wide range of therapeutic areas, including cardiovascular, antidiabetic, CNS, gastrointestinal, dermatology, and nutrition. Every batch undergoes stringent in-process controls and quality testing in our advanced QC laboratory. With dedicated staff, specialized equipment, and a robust documentation system, we consistently meet WHO-GMP standards, delivering safe, effective, and high-quality medicines for both domestic and international markets.