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.

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/