In addition to the pressure of maintaining a positive public image, pharmaceutical companies have EHS compliance obligations from regulatory agencies, as well as a separate set of obligations with the Food and Drug Administration (FDA). FDA regulations are complex and stringent, adding to the burden of EHS staff, and increasing demand on the organization to remain in compliance and subsequently avoiding bad press.
Pharmaceutical companies are implementing the Enviance System as an all-in-one solution that covers their entire compliance management program, maximizing their investment and saving time by streamlining processes and improving data quality. Pharmaceutical software like this has a number of important benefits.
Most pharmaceutical companies have compliance requirements that span a variety of regulatory agencies and cover everything from air, water, and waste to vaccine sampling by the FDA. Seeking to ease the burden on your compliance staff, without requiring additional support from the Information Solutions department? The Enviance System is the answer. Its Internet platform and ability to handle tasks, calculations, and reporting for multiple regulatory agencies are big benefits. Data only needs to be entered once, and is manipulated to fit any requirement:
- Title V (Air Compliance)
- Effluent Discharge Monitoring Report (DMR)
- Infectious and hazardous waste tracking
- FDA's current Good Manufacturing Practice (cGMP)
- Sustainability and annual shareholder reporting
- Green reporting in Canada
- And more
To find out more about current uses of the Enviance System by pharmaceutical industry clients, see our
case studies or
Resource Library.
If you are a pharmaceutical company and are facing compliance pressures or are managing Green House Gas and Sustainability initiatives,
contact Enviance for a complimentary assessment.