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.