In the highly regulated pharmaceutical industry careful quality control and documentation is expected throughout all areas of operations. This includes EHS-related compliance. Corporate sustainability reporting, U.S. Title V permit management, ISO 14001 conformance and corporate sustainability reporting are just a few of the new environmental management challenges faced by pharmaceutical EHS staff. ESP's opsEnvironmental™ software helps you respond effectively to these and other pharmaceutical industry environmental information management challenges. The software helps you maximize operational efficiency while assuring compliance with both internal corporate and regulatory standards. A fully scalable system lets you easily manage emissions in diverse locations. Web-based task management and reporting lets users throughout the facility or global corporation all access, input and retrieve data from a single, centralized system. And automated, escalating time-driven and data-driven e-mail notifications enable proactive environmental management and increased compliance visibility.

Typical environmental challenges in the pharmaceutical industry

Challenge	ESP Solution
Sustainability and GRI Data Collection	opsEnvironmental™ makes collecting data from all your facilities efficient and easy, allowing corporate wide metrics data entry and reporting from the web.
Annual Certification of U.S. Title V permit/s	Task management helps ensure that all permit conditions are tracked and the data is available for easy certification of permit compliance. Optional “Evergreening” ensures that your system receives automatic, regular updates whenever regulations change.
U.S. Pharmaceutical MACT	The software tracks the monitoring, recordkeeping and reporting requirements required by the MACT standard. Easily track your Pharmaceutical Manufacturing Process Unit/s (PMPU).
Wastewater Treatment Plant Compliance Reporting	The opsEnvironmental™ water module makes easy work of integrating with your LIMS system to import the lab data needed to generate necessarily regulatory reports.