IT Applications

Specializing within Pharma, Biotech and Medical Device Industry Pharma IT possess deep insight into the sector specific IT applications used. Below an indication of the applications we are working with, but the list is by no means exhaustive so don’t hesitate to contacts us to discuss you needs:

  • Electronic Document Management Systems (EMDS)
  • Training Management Systems
  • Records Management Systems
  • Change Management Systems
  • Test Management Systems
  • Security Management Systems
  • Master Data Management Systems
  • Laboratory Information Management Systems
  • Clinical Trial Management Systems (CTMS)
  • eCRF Systems
  • eTMF Systems
  • SEND/CDICS Systems
  • Submission Systems
  • Regulatory Information Management Systems (RIMS)
  • ERP Systems
  • Product Life Management Systems
  • Serialisation
  • Safety and Pharmacovigilance Systems
  • Signal Detection Systems
  • Pharmacovigilance System Master File Systems (PSMF)
  • Healthcare Professional Management Systems (HCP/HCO/PO)
  • Interlectual Property Management Systems
  • Service Management Systems

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

Meet the IT Applications team:

Business Consultant
Sara Halsskov

Holds more than 15 years of experience working in the pharmaceutical industry, working with IT systems and processes, primarily within Regulatory Affairs.  Sara has performed the role as Clinical Publisher, Regulatory Application Professional, eSubmission Manager, Senior QMS Professional/Project manager within Regulatory Affairs and Release Manager as part of System Management.

ITIL Foundation Certification, SOP Expert training, Writing effective standard operating procedures and other process documents (CfPIE), Computer Validation, Veeva
Business Consultant
Peter Noes

Information technology professional with more than 13 years of experience from the pharmaceutical industry. Extensive business understanding and experience from IT projects mainly within the areas of Regulatory Operations – eSubmission (eCTD), Electronic Documents Management Systems (EDMS), Regulatory Information Management Systems (RIMS), XEVMPD and IDMP. Broad experience with project management, system administration and system implementation and with establishing and optimizing business processes within GxP areas.

Certified Veeva Vault Administrator, Computerized System Validation/GAMP5 and GDPR Foundation, Veeva
BenedikteMarieDueBW
Quality & Compliance Consultant
Benedikte Marie Due

More than 10 years of experience with IT compliance. Working as Validation Track Lead in IT implementation projects and as Business Consultant in system operation and maintenance.

Experience primarily with corporate GxP systems within the Regulatory, Quality and R&D area. Also experience with international projects, external vendors and offshore personnel.

Certified in Computerized System Validation/GAMP5, Certified Veeva Vault Administrator, Veeva
Business Consultant
Luise Søgaard Rosendahl

Holds extensive experience in the pharmaceutical industry working with IT Service Management, IT implementation projects, and IT Transition and Transformation programmes. Has played pivotal roles in IT system management organisations responsible for applications supporting Product Supply. Furthermore hands on experience as Business Consultant, IT Management SME, and Track Lead as part of a Management Consultancy organization.

ITIL®V3 Foundation, ITIL®V3 Intermediate RCV, NLP Business Practitioner, SAFe Agilist
Business Consultant, Quality & Compliance Consultant
Lene Hyldgaard Jensen

Experienced Business Consultant with more than  10 years’ experience in the pharmaceutical industry working in various business partnering roles, preparing business analysis, facilitating workshops, transforming business requirements into IT development and implementation projects and delivering subject matter expert assignments, especially in the Regulatory area. Hands on Quality and Compliance experience with GxP IT systems and writing of Standard Operating Procedures.

ISPE GAMP 5, ITIL, Project Management, GLP, GCP, Veeva
JakobJuulRasmussen
Partner, Management Consultant
Jakob Juul Rasmussen
+ 45 24 34 26 55

IT Program/Project Manager with 16 years of experience within the pharmaceutical industry, finance and the public sector. Experience with infrastructure, service delivery management, application development, SOA and SAP projects

Project and Program Management certified in IPMA level A, PMP, MoP, PRINCE2, MSP and Professional SCRUM master
JRK 2017 BW
Business Consultant
Jannie Rosenkjær Melbye

Senior Pharma Consultant with 11 years’ experience within document/information and application management. 17 years’ of experience in the field between IT and business. Experience with GxP, application management – especially document management, functional and technical support, test and validation. Furthermore, experience within ITIL, vendor management, communication with end users, transition and application management.

Certified in ITIL, Computerized System Validation, SAFe Agilist