About Saar Biotech

Saar Biotech is one of the leading pharmaceuticals manufacturing company in India. We use latest techniques and technologies for performing test. We are engaged in third party manufacturing of varied pharmaceutical formulations and also manufactured products for domestic and international market. Our product range consists Syrups, Dry syrups, suspensions, Nasal spray, Roll On, Lotions, Drops, Ointment, Glycerine and Shampoo. Our plant is large, well-designed and comply with global requirements.

Infrastructure, processes and systems at our plants support a flexible product mix and quick product changeovers. We have wide product range which comprises Anti-Fungal, Anti-Bacterial, Anti-Inflammatory, Antitussive and Dermatological products. At our manufacturing site, the latest analytical instruments and tightly monitored quality assurance and quality control systems ensures consistent quality of our products.

Saar Biotech Pvt. Ltd. is a distinguished WHO-GMP certified pharmaceutical manufacturing company, renowned for its unwavering dedication to quality and innovation. Since our inception in 2005, we have been at the forefront of the industry, operating from our state-of-the-art manufacturing facility in Baddi, complemented by our centrally located head office in Chandigarh.

With over 15 years of experience, we have earned the trust of a diverse clientele comprising over 1700 companies, solidifying our position as a trusted partner in the pharmaceutical landscape. Our extensive product range encompasses a wide array of pharmaceutical formulations, including Oral Liquids, Ointments, Sprays, Mouthwash, and Paste, catering to various therapeutic segments.

At Saar Biotech, quality is our foremost priority. Our manufacturing processes adhere to stringent quality standards, ensuring that each product meets regulatory requirements and surpasses customer expectations. Our commitment to excellence extends beyond manufacturing; it permeates every aspect of our operations, from research and development to customer service.

Driven by a passion for innovation and a commitment to customer satisfaction, we continually strive to enhance our capabilities and expand our product portfolio. With a team of dedicated professionals and cutting-edge technology, we aim to redefine pharmaceutical manufacturing, setting new benchmarks for quality, efficacy, and reliability.

Partner with Saar Biotech and experience the difference in pharmaceutical excellence. Together, let's embark on a journey towards a healthier, brighter future.

WHO Certification

The "World Health Organization (WHO)" is a specialized agency of the "United Nations (UN)" that is concerned with international public health.

WHO identifies its role as:

Providing leadership on matters critical to health and engaging in partnerships where joint action is needed.

Shaping the research agenda and stimulating the generation, translation and dissemination of valuable knowledge.

Providing technical support, catalyzing change, and building sustainable institutional capacity; and

Monitoring the health situation and assessing health trends.

GLP Certification

Good Laboratory Practice (GLP) is an internationally recognized set of principles, which provides a framework within which laboratory studies are planned, performed, monitored, recorded, reported and archived.

Laboratories undertake studies to generate data, on the basis of which, hazards and risks to users, consumers and others including environment, can be assessed. Studies can be conducted on a variety of subjects including pharmaceuticals, agro-chemical, veterinary medicines, industrial chemicals, cosmetics, food, food additives and biocides.

GMP Certification

Good manufacturing practice" or "GMP"is part of a quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices. GMPs are guidelines that outline the aspects of production and testing that can impact the quality of a product.

Many countries have legislated that pharmaceutical and medical device companies must follow GMP procedures,and have created their own GMP guidelines that correspond with their legislation.