Security

Pharma IT is experienced in Security Management. We have consultants working with general security management activities ensuring the requirements for establishing, implementing, maintaining and continually improving an Information Security Management System.

We have certified consultants in the General Data Protection Regulation area that can help setting the right level of compliance. See more here.

Besides that, we can Implement and Audit against ISO27001 standard.

Our services include:

  • Risk Assessments
  • Business Impact Assessment
  • Data Privacy Impact Assessment
  • Software Vendor Audit
  • Built and maintain Standard Operating Procedures and related processes
  • Build and maintenance of an Information Security Management System (ISMS)

We hold certifications within CISSP (IT security), ISO27001, CISA (Information System Audit), CISM (Security Manager), GxP, Computerized System Validation, Data Integrity, ALCOA principles, 21 CFR Part 11 / EU Annex 11

If you need support don’t hesitate to contact us.

Meet the Security team:

Business Consultant
Steen Lindebjerg

IT Program/Project Manager and Senior Pharma Consultant within Identity Management and GDPR with more than 20 years of experience from the IT industry within Pharmaceutical, Finance, Food and Public sectors. Experience with wide range of projects and operation in Infrastructure, IAM & Security, Application development, process optimization and IT service management.

SAFe 4 Agilist, PRINCE2, ITIL, GDPR Practitioner, CIPP/E and Certified Engineer in Microsoft Infrastructure MSCE and Nowell Network CNE
DanAndersenR
Quality & Compliance Consultant
Dan Andersen

30 years of pharma experience from multiple area of business and levels of responsibility with a constant focus of delivering compliant solutions. Hands on experienced as a Security Manager, QA, Compliance Specialist, Validation Specialist, Project Manager and Process Technician.

Certified in CISSP (IT security), CISA (IS Audit), CISM (Security Manager), GxP, Computerized System Validation, 21 CFR Part 11 / EU Annex 11, LEAN and ITIL, Veeva