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Welcome To NANDANI MEDICAL LABORATORIES PVT LTD

Our Primary Focus is to address the healthcare needs of patients and enhance their quality of life

NANDANI MEDICAL LABORATORIES PVT LTD, which is WHO-GMP & ISO 9001-2015 certified manufacturing plant based out of ‘INDORE’, the commercial capital of central India.

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Welcome To NANDANI MEDICAL LABORATORIES PVT LTD

Our Primary Focus is to address the healthcare needs of patients and enhance their quality of life

NANDANI MEDICAL LABORATORIES PVT LTD, which is WHO-GMP & ISO 9001-2015 certified manufacturing plant based out of ‘INDORE’, the commercial capital of central India.

WORK PROCESS

Our Expertise

At Nandani Medical Laboratories, our expertise in the pharmaceutical industry is unrivaled. With years of experience and a dedicated team of highly skilled professionals, we have established ourselves as leaders in the field. Our in-depth knowledge and understanding of pharmaceutical processes, regulations, and market dynamics enable us to deliver exceptional results.
Excellence Worldwide

Delivering Sterile Excellence Worldwide (Export)

At Nandani Medical laboratories we take pride in our global presence, serving customers and healthcare providers around the world. With our commitment to excellence, quality, and innovation, we have established a strong foothold in various regions, making a positive impact on the global healthcare landscape.With a remarkable 25 plus years of experience serving throughout India as well as in other countries, we are one of the most trusted Pharmaceutical manufacturing organizations in India. Our products are being supplied to every nook and corner of the country, having a potent hold over domestic and international markets.CTD and A-CTD dossiers available as per guideline for most of the products.We have spread our wings on international platforms with direct and merchant exporter supplies to African, Asian, CIS and Latam American countries. We are Present in Brazil, Columbia, Chile, Venezuela, Peru, Ecuador Uzbekistan, Kazakhstan, Tajikistan,Azerbaijan,Kenya,Ivory Coast, Liberia Gambia, Burundi, Myanmar, Cambodia, Yemen etc
Contract Manufacturing

Urge to Contract Manufacturing

We have a unique opportunity to provide manufacturing services to pharmaceutical companies seeking to outsource their production needs. Our contract manufacturing services, emphasize the value in terms of quality, reliability, and regulatory compliance Today we are one of the paramount and most trusted Pharma giants in India, having bagged multi-fold awards and recognitions in our crown to boast with; as on date our human & veterinary division have range of more than 1000+ drugs of the below ranges.

Sl.No

Range

Production capacity per day

1

Liquid Injection Vials

50000 Nos.

2

Liquid Injection ampoules

2 lacs  Nos.

3

Dry Injections

1 lac  Nos.

Research & Development

Research & Development

Our R&D teams focus on developing new formulations or improving existing ones for sterile pharmaceutical products. This involves research on novel drug delivery systems, stability studies, compatibility assessments, and optimization of formulation parameters to enhance product efficacy, safety, and stability.it plays a vital role in optimizing manufacturing processes for sterile products.

This includes studying different process parameters, evaluating the impact of process changes on product quality and sterility, and identifying opportunities for efficiency gains. The goal is to streamline and enhance the manufacturing process while maintaining the required sterility and quality standards.

Sterile Processing Techniques

Sterile Processing Techniques

Sterile processing techniques are applied to the unit in which a set of practices and procedures are employed to maintain a sterile or aseptic environment in healthcare facilities or pharmaceutical manufacturing units. These techniques are crucial for preventing contamination and ensuring the safety of patients, healthcare workers, and the products being manufactured. Adhering to these sterile processing techniques like Cleanroom Design and Maintenance,Gowning and Sterile Attire, Environmental Monitoring, Aseptic Techniques, Training and Education etc we prevent contamination, maintain sterility, and ensure the safety and efficacy of products produced in sterile manufacturing units or provided in healthcare settings. Compliance with regulatory guidelines and best practices is essential for successful sterile processing operations.
Quality Assurance

Quality Assurance, Control & Regulatory Compliance

Quality assurance and control play a vital role in ensuring the safety, efficacy, and consistency of products produced in a sterile manufacturing unit. By implementing comprehensive quality assurance and control measures,our sterile manufacturing unit maintains high standards of product quality, comply with regulatory requirements, and ultimately ensure the safety and effectiveness of the sterile products produced.we apply Quality Management System (QMS), GMP Compliance, Batch Record Documentation, Process Validation, Quality Control Testing, Deviation Management, to assure our quality products.We Ensure compliance with regulatory guidelines and standards such as FDA , cGMP or other applicable regulations. Conduct regular internal audits and inspections to maintain compliance.

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