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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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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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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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Bharat Serums and Vaccines Limited went live with APQR System

AmpleLogic is delighted to announce the successful implementation of Annual Product Quality Review (APQR) System at Bharat Serums and Vaccines Limited (BSV) 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. AmpleLogic Annual Product Quality Review (APQR) Software helps to automate and streamline the paper-based documentation required for review of every batch product manufactured. This PQR Solution also meets the compliance requirements and ensure the data integrity. Our GMP Compliance 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, GMP, MHRA, ISO, and other regulations and standards that apply to their drug products. About Bharat Serums and Vaccines Limited Bharat Serums And Vaccines Limited is one of the fastest growing bio pharmaceutical companies in India. BSV is amongst the top 10 Biotech companies in India. The Company has in its portfolio over 145 brands. The company has over 1000 employees selling its products across the country. Our brands are marketed all over India and exported to over 70 countries across the world. BSV has used its scientific resources to develop a range of biological, biotech and pharmaceutical products. Today, as we influence patient outcomes in the therapeutic areas of Women’s health and Critical Care and IUI-IVF, we have the privilege of being a partner of choice. For more information, visit https://bsvgroup.com/

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indoco

Indoco Remedies Goes Live with AmpleLogic DMS System

AmpleLogic is delighted to announce the successful implementation of Electronic Document Management (EDMS) System at Indoco Remedies. 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 Indoco Remedies Indoco Remedies Ltd. is a pharmaceutical company based in India. The company was founded in 1947 and has since then grown into a leading player in the Indian pharmaceutical industry. Indoco Remedies is primarily engaged in the development, manufacture, and marketing of a wide range of pharmaceutical products including active pharmaceutical ingredients (APIs), finished dosage forms, and biologics. Indoco Remedies has a diverse product portfolio that includes medicines for various therapeutic areas such as anti-infectives, pain management, respiratory care, gastroenterology, cardiovascular, and central nervous system disorders. The company’s products are sold in India and exported to over 55 countries across the world. Indoco Remedies has a strong research and development (R&D) focus and invests heavily in developing new products and technologies. The company has state-of-the-art R&D facilities that are equipped with advanced analytical, process development, and formulation development capabilities.

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fdc

Quality Management System Goes Live at FDC Limited

FDC Ltd Goes Live with AmpleLogic Quality Management System (QMS) AmpleLogic is delighted to announce the successful implementation of Electronic Quality Management System (QMS) at FDC Limited 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. AmpleLogic web-based Electronic Quality Management System (EQMS) which enables them to manage, monitor and control the required quality processes. This Digital QMS Software will also streamline the process of meeting regulatory compliance standards and in ensuring data integrity. Our GMP Compliance 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, GMP, MHRA, ISO, and other regulations and standards that apply to their drug products. About FDC Lmited FDC carries forward the flaming spirit of it’s first dream, achieving accreditations from the US-FDA, UK-MHRA, MCC-RSA, and the UAE, to cite a few. FDC is a forerunner in the manufacture of ORS and Ophthalmics, by setting up, globally approved, multi-location manufacturing facilities for Active Pharmaceuticals Ingredients (APIs) and Finished Dosage Forms. These facilities are located at Roha, Waluj and Sinnar in Maharashtra, Verna in Goa and Baddi in Himachal Pradesh. FDC has over 300 products and exports the same to over 50 countries, worldwide. FDC strives to explore, innovate and integrate solutions with modern technology, empowering talent and expanding healthcare horizons for a better quality of life to millions globally. Since 1936, FDC has been dedicated to innovating, manufacturing, and marketing high-quality healthcare products, in India, and abroad. FDC has over 300 products and exports to over 50 countries worldwide. For more information, visit https://www.fdcindia.com/

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umedica

QMS Solution implementation at Umedica Laboratories Pvt. Ltd

Umedica Laboratories Pvt. Ltd Goes Live with AmpleLogic QMS Solution AmpleLogic is delighted to announce the successful implementation of Electronic Quality Management Software Solution (QMS) 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.AmpleLogic web-based Electronic Quality Management Solution (EQMS) which enables them to manage, monitor and control the required quality processes. This Electronic EQMS Software will also streamline the process of meeting regulatory compliance standards and in ensuring data integrity. Our GMP Compliance 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, GMP, MHRA, ISO, and other regulations and standards that apply to their drug products About Umedica Laboratories Pvt. Ltd UMEDICA is one of the leading manufacturer of pharmaceutical formulations & export house in India, offering a broad spectrum of chronic and acute therapies. Since its inception, UMEDICA has established itself as a company delivering products meeting international quality standards. UMEDICA is a Government recognized Export House, with global business in over 85 countries viz US, EU, Canada, Australia, Middle East, Central & South American countries, Africa, Asian & CIS countries. For more information, visit https://www.umedicalabs.com/

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serum inst

Serum Institute of India Pvt. Ltd Goes Live with AmpleLogic LMS Software

Serum Institute of India Pvt. Ltd Goes Live with Amplelogic LMS Software AmpleLogic is delighted to announce the successful implementation of eLMS Software at Serum Institute of India Pvt. Ltd 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. Based on the client’s requirements, AmpleLogic offered its proven Learning Management Software System that could be easily extended to address the needs of our client requirements. AmpleLogic Employee Training Management Software is a web-based solution that enables you to easily develop and manage learning programs including instructor-led classroom sessions, on-the-job training, and induction programs as well as track, report and deliver them online and offline AmpleLogic eLMS Software is designed to effectively and efficiently automate all your employee training programs. This LMS Solution gives you a complete, real-time visibility of training programs. Our GMP Learning Management Software provides your company with a complete audit trail and is fully compliant with 21 CFR PART 11, FDA, MHRA, EU Annex 11 and other regulatory standards. Are you interested in learning more about our GMP and SOP Training Management Solution? Click here to explore About Serum Institute of India Serum Institute of India Pvt. Ltd. is the world’s largest vaccine manufacturer by number of doses produced and sold globally (more than 1.5 billion doses) which includes Polio vaccine, Diphtheria, Tetanus, Pertussis, Hib, BCG, r-Hepatitis B, Measles, Mumps, Rubella as well as Pneumococcal and Covid-19 vaccines. Vaccines manufactured by the Serum Institute are accredited by the World Health Organization, Geneva and are being used in around 170 countries across the globe in their national immunization programs, saving millions of lives throughout the world. Serum Institute of India is ranked as India’s No. 1 biotechnology company, manufacturing highly specialized life saving biologicals like vaccines using cutting edge genetic and cell based technologies, antisera and other medical specialties For more information, visit https://www.seruminstitute.com/

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Bharat Serums and Vaccines Limited Goes Live with AmpleLogic LMS System

Bharat Serums and Vaccines Limited Goes Live with AmpleLogic LMS System AmpleLogic is delighted to announce the successful implementation of LMS System at BSV Group 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. Based on the client’s requirements, AmpleLogic offered its proven Learning Management Software System that could be easily extended to address the needs of our client requirements. AmpleLogic GMP Training Software is a web-based solution that enables you to easily develop and manage learning programs including instructor-led classroom sessions, on-the-job training, and induction programs as well as track, report and deliver them online and offline AmpleLogic LMS Software is designed to effectively and efficiently automate all your employee training programs. This LMS Solution gives you a complete, real-time visibility of training programs. Our Learning Management Solution provides your company with a complete audit trail and is fully compliant with 21 CFR PART 11, FDA, MHRA, EU Annex 11 and other regulatory standards. About Bharat Serums And Vaccines Limited Bharat Serums And Vaccines Limited is one of the fastest growing bio pharmaceutical companies in India. BSV is amongst the top 10 Biotech companies in India. The Company has in its portfolio over 145 brands. The company has over 1000 employees selling its products across the country. Our brands are marketed all over India and exported to over 70 countries across the world. BSV has used its scientific resources to develop a range of biological, biotech and pharmaceutical products. Today, as we influence patient outcomes in the therapeutic areas of Women’s health and Critical Care and IUI-IVF, we have the privilege of being a partner of choice. For more information, visit https://bsvgroup.com/

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Slayback Pharma Goes Live with AmpleLogic EDMS Solution

Slayback Pharma Goes Live with AmpleLogic EDMS Solution AmpleLogic is delighted to announce the successful implementation of EDMS Solution at Slayback Pharma 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. Based on the client’s requirements, AmpleLogic offered its proven Electronic Document Management Software System that could be easily extended to address the needs of our client requirements. AmpleLogic EDMS Solution is a web-based document management solution that allows users to create, manage, retrieve, upload, track and share documents in a highly secure environment. The DMS Solution can enable greater control over how documents are stored, better visibility for audits, improved retention policy for different departments and a simplified data structure. Our Electronic Document Management Solution provides your company with a complete audit trail and is fully compliant with 21 CFR PART 11, FDA, MHRA, EU Annex 11 and other regulatory standards. About Slayback Pharma Slayback Pharma is a New Jersey-based company focused on complex generic and specialty pharmaceutical products with a team of 85 employees and operations in the U.S., India and Europe. Since its inception in 2011, Slayback has demonstrated a spectacular track record of numerous sole first-to-file ANDAs, 505(b)(2)s and complex generic filings, approvals and launches. For more information, visit https://slayback-pharma.com/

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