PharmaLTx Software Development EDC EMR eCRF eREGISTRY Cloud Based

ABOUT US

PharmaLTX has a development team that has many years of development experience using the latest technologies to ensure that our development platforms are current and relevant to the industry changes. Although we abide by the strict rules set out by the FDA on developing applications storing sensitive information, we are forward thinking in our processes and venture to produce market relevant and user friendly systems.

ABOUT US

PharmaLTX (Pty) Ltd is an eClinical Solutions Company launched in 2015 to provide EMR (Electronic Medical Records) & EDC (Electronic Data Capture) solutions within clinical research, eliminating the problems inherent to paper-based data collection methods. PharmaLTX has a development team that has many years of development experience using the latest technologies to ensure that our development platforms are current and relevant to the industry changes. Although we abide by the strict rules set out by the FDA on developing applications storing sensitive information, we are forward thinking in our processes and venture to produce market relevant and user friendly systems.

OUR APPROACH

Our EMR solution provides cleaner data more quickly by eliminating paper-based data collection – reducing costs and time to market for pharmaceutical and medical device companies. Our solution maintains the workflow of paper while allowing fast, secure transmission of source data via an online interface.

Our uniquely designed framework allows all the stakeholders within the product development lifecycle to work on a central, cloud-hosted platform sharing the same database. The entire portal is governed using role-based access and has been implemented and built with the FDA’s CFR Part 11 regulations and HIPAA privacy laws as foundation.

OUR APPROACH

Our EMR solution provides cleaner data more quickly by eliminating paper-based data collection – reducing costs and time to market for pharmaceutical and medical device companies. Our solution maintains the workflow of paper while allowing fast, secure transmission of source data via an online interface. Our uniquely designed framework allows all the stakeholders within the product development lifecycle to work on a central, cloud-hosted platform sharing the same database. The entire portal is governed using role-based access and has been implemented and built with the FDA’s CFR Part 11 regulations and HIPAA privacy laws as foundation.