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US Pharma Lab

US Pharma Lab Chooses AmpleLogic Stability Management Software to implement at their facilities

AmpleLogic is pleased to announce that US Pharma Lab (United States) has chosen AmpleLogic Stability Management Software for automating and managing their stability process.

To learn more, or request a free demo of AmpleLogic Stability Study Management Software, contact us today at info@amplelogic.com

About US Pharma Lab

Us Pharma Lab Founded in 1996, the company is head-quartered in North Brunswick, New Jersey and has 20 years of experience providing custom formulations, manufacturer, and supplier of premium dietary supplement ingredients, premixes, and products to a list of clientele around the world.

They have served clients in the pharmaceutical and nutraceutical industry with great success. As a global company, they have the ability to manufacture ingredients to meet your needs. Today, the company spans the globe with a manufacturing imprint of over 500,000 sq. ft. within its seven NSF cGMP certified and US FDA audited facilities located in the United States, India, and China.

For more information, visit https://www.uspharmalab.com/

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Windlas Goes Live with AmpleLogic Electronic Document Management System

Windlas Goes Live with AmpleLogic EDMS System AmpleLogic is delighted to announce the successful implementation of the Electronic Document Management (EDMS) System at Windlas. We would like to take the opportunity to thank everyone involved in this implementation for their support, enthusiasm, and hard work during the course of this project. Our GMP Software Solutions is purpose-built for the life sciences sector, and eases the burden of managing quality processes, as well as solving non-quality related issues within your company and all solutions are compliant with FDA, WHO, EU Annex 11, cGMP, MHRA, ISO, and other regulations and standards that apply to their drug products. To learn more about the electronic document management software (EDMS) offered by AmpleLogic, please feel free to contact us Explore Our DMS Software About Windlas Windlas Biotech is renowned for its unwavering commitment to providing top-notch pharmaceutical development services, large-scale manufacturing services, and authentic yet affordable products to customers and consumers worldwide. With a firm belief in the power of innovation and quality, the company has become a trusted name in the pharmaceutical sector. At the heart of Windlas Biotech’s success are its dedicated employees. With a workforce of 954 talented individuals, the company operates from four state-of-the-art manufacturing facilities nestled in the beautiful city of Dehradun, Uttarakhand, India. These facilities serve as the backbone of the company’s operations, ensuring the production of high-quality pharmaceutical products. But it doesn’t stop there. Windlas Biotech has also built an extensive salesforce and distribution network that spans across 14 states. This strategic approach allows the company to market its own manufactured nutraceutical, pharmaceutical, and ayurvedic products directly to semi-urban and rural communities. By cutting out middlemen and focusing on direct outreach, Windlas Biotech aims to make its authentic products accessible to those who need them most, at affordable prices. To further strengthen its commitment to transparency and authenticity, Windlas Biotech operates under the registered name of Windlas Biotech Limited (formerly known as Windlas Biotech Private Limited). This name change reflects the company’s growth and transformation over the years while retaining its core values and dedication to providing quality healthcare solutions.

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umedica (1)

Umedica successfully went live with EDMS System

AmpleLogic is delighted to announce the successful implementation of Electronic Document Management (EDMS) System at Umedica Labs We would like to take the opportunity to thank everyone involved in this implementation for their support, enthusiasm, and hard work during the course of this project. Our GMP Software Solutions is purpose-built for the life sciences sector, and eases the burden of managing quality processes, as well as solving non-quality related issues within your company and all solutions are compliant with FDA, WHO, EU Annex 11, cGMP, MHRA, ISO, and other regulations and standards that apply to their drug products. To learn more about the electronic document management software (EDMS) offered by AmpleLogic, please feel free to contact us About Umedica Labs UMEDICA is one of the leading manufacturer of pharmaceutical formulations and  export house in India, offering a broad spectrum of chronic and acute therapies UMEDICA’s manufacturing facility, located in Vapi, Gujarat is a WHO GMP approved, US FDA, EU, Health Canada, TGA & UAE MoH approved facility. The facility has also been audited and approved by Regulatory authorities of various countries viz. USA, EU, Australia, Canada, UAE, Zimbabwe, Ethiopia, Tanzania, Nigeria, Uganda, Kenya, Ghana, Ivory Coast, Malawi etc.

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laurus labs (1)

Laurus Labs chooses AmpleLogic to implement Calibration & Preventive Maintenance Software

Laurus Labs chooses AmpleLogic for the implementation of another GMP Compliant solution – Calibration and Preventive Maintenance Software as part of their digital transformation journey. It helps them to fully digitize their manual paper-based process and streamline operations to increase efficiency and reduce errors.  Calibration and PM Software (CAPS) is AmpleLogic’s 4th product that went live at Laurus after BIMS, LMS & DMS.  Its been 6 years working with Laurus Labs and both teams still continue the same energy and commitment from the first Implementation. With 100+ Global clients, our quality solutions are trusted by Fortune 500 companies. With rapid deployment and faster go-to-market speed, our solutions help the clients achieve compliance. Our GMP Compliance Solutions is purpose-built for the life sciences sector, and eases the burden of managing quality processes, as well as solving non-quality related issues within your company and all solutions are compliant with FDA, WHO, MHRA, ISO, and other regulations and standards that apply to their drug products. To learn more, or request a free demo of AmpleLogic Calibration Management Software, contact us today at info@amplelogic.com About Laurus Labs Laurus is a leading research based pharmaceutical and biotechnology company, which aims to improve the quality of medical services around the world. They work with some of the top generic pharmaceutical firms and sell their APIs in 56 countries with major focus areas include anti-retroviral, Hepatitis C and Oncology drugs. Laurus’s facilities are certified and approved by WHO, USFDA, NIP Hungary, PMDA, KFDA and BfArM. They have a strong R&D and API manufacturing capabilities. For more information, visit https://www.lauruslabs.com/

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