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AmpleLogic eQMS Solution implementation ‘Go-Live’ at Medopharm

AmpleLogic eQMS Solution implementation ‘Go-Live’ at Medopharm

We are pleased to announce that Medopharm successfully went live with AmpleLogic Electronic Quality Management Software (EQMS) for use at their facility. AmpleLogic eQMS will help enable continuous improvement, and help achieve higher operating efficiency and improve productivity. AmpleLogic EQMS Solution will also increase transparency of information allowing users to make fact-based decision making driven by the data gathered from a comprehensive eQMS system.

Contact us for more information about how your organization can benefit from AmpleLogic Electronic Quality Management Software

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windlas (1)

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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