NEW: 256 pages book to be published in October 2008:

International IT Regulations and Compliance

Segalstad, Kierulf, Langseth-Manrique, and Storstein: Free Digitoxin in Normal and Albumin-Deficient Serum as estimated by Centrifugal Ultrafiltration, Clinical Chemistry 4 (1988) 766-777.

Segalstad and Synnevåg: A practical guide to validating LIMS, Laboratory Information Management 26 (1994) 1-12 (Tutorial).

Segalstad: Quality Assurance of Computer Systems What is needed to comply with ISO 9000, GMP, GLP, and GCP?, Laboratory Automation and Information Management 31 (1995) 11-24.

Segalstad: Quality Assurance of Computer Systems Compliance with GMP, GLP, GCP and ISO Standards, LIMS Letter Vol II - Issue I, Spring 1996.

Segalstad: LIMS 95 - LIMS 1995 - A delegate’s view, Laboratory Automation and Information Management 31 (1995) 151-153.

Segalstad: Vendor audits for Computer Systems: An ISO 9000-3 approach, Laboratory Automation and Information Management 32 (1996) 23-31.

Segalstad: Validation of computer databases for GxP. Chapter in book Good Research Practices, edited by Nigel Dent, Butterworth and Heineman (1996) 475-485.

Segalstad: Book review, Laboratory Automation and Information Management, 1996.

Segalstad: Supplier Auditing and Software, European Pharmaceutical Review Vol. 1 Issue 3, (1996) 37-44.

Segalstad: Quality Assuring the Laboratory Computer - keeping it in compliance. Proceedings from 18th Nordic Conference on Measuring Techniques, November 1996.

Segalstad: Outsourcing work in the pharmaceutical industry - a challenge to quality, European Pharmaceutical Review Vol.1 Issue 4, (1996) 59-63.

Segalstad: Validation Issues Update, LIMS/Letter Spring 1997, 6-7.

Segalstad: Can You Rely on Your Information Technology, Inside Laboratory Management, Vol. 1 No. 4 (May 1997) 16-17.

Segalstad: Kvalitetssikring av laboratorier - Ufullstendig uten validering av IT-systemer. (Quality assurance of laboratories - incomplete without validation of IT systems), Kjemi 8, 1997, 16-18.

Segalstad: Software validation according to EU GMP Annex 11, European Pharmaceutical Review, Vol. 2 Issue 4, (1997) 55-64.

Segalstad, Florén, Nilsson: Choosing and installing the right LIMS, Scientific Computing World, Issue 39 June 1998, 25-26. (Re-written by the journal’s editor without authors’ approvals)

Segalstad: Cr 2000-problemet: Datakaos slett ikke umulig (Year 2000: Data chaos not inconceivable), Kjemi 6, 1998, 11.

Segalstad: LIMS: M is for Management, Process Information Technology, June 2000 54-56.

Segalstad: The WWW (Who-Why-What) of 21 CFR Part 11 Electronic Records and Electronic Signatures, European Pharmaceutical Review Vol. 5 Issue 2 (2000) 69-74.

Segalstad: The User Requirements Specification – The most Important Tool in the Validation, Scientific Computing and Instrumentation, Fall 2000 (24-25)

Segalstad: Development Qualification: Selecting the right LIMS vendor, European Pharmaceutical Review, Vol. 5 Issue 4 (2000) 58-61 Also published in: American Pharmaceutical Review, Vol. 3, Issue 4 Winter 2000-2001 (84-87)

Segalstad: Instrument validation, Managing the Modern Laboratory In press spring 2001

Segalstad: Elektroniske data og elektronisk signatur, (electronic data and electronic signatures) Kjemi, April 2001 (9-12)