Pharmaceutical Data Security Solutions
Achieve Data Privacy Compliance
Protect IP and PII
GRC / Risk & Audit Reports
Sensitive clinical trial result information is tracked and audited.
Research / CRO
Contract Research Organizations (CRO) provide clinical-study and clinical-trial research for new drugs and medicine that is shared with the sponsoring company. Information is also shared with manufacturers, laboratories, and university scientists.
R&D / IP & New Technology
Guidelines produced by the R&D team contain critical Intellectual Property (IP) related to the manufacturing process and are often shared with suppliers. Product dossiers contain details of a new pharmaceutical product and are shared with multiple internal and external parties.
QA / Reports & Incident Management
The Issue Management team manages concerns between departments and produces highly sensitive documents containing compliance and quality issues such as patient safety risk.
Patent application processes and lawsuits require the exchange of sensitive data with third parties.
Legal / Trade Schemes
Highly confidential schemes containing incentive plans are shared with Retailers and Distributors for a particular product.
HR / Employee Data
Employee data is shared across business units and with outsourced agencies such as payroll and benefit companies.