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Miscellaneous

References

Pages 109-116 | Published online: 29 Mar 2011

References

  • AACC, Laboratory Quality Assurance Sub-committee. Proposed AACC position paper on off-site laboratory testing. Manuscript, 1985:4 pp.
  • Anderson JR, Linsell WD, Mitchell FM. Guidelines on the performance of chemical pathology assays outside the laboratory. Br Med .1 1981;282:743.
  • Arends J, Uldall A. The reliability of preg-nancy tests performed by trained and un-trained persons. Dan Med Bull 1977;24: 115–6.
  • Ashby JP, ed. The patient and decentralized testing. Proceedings of the ECCLS confer-ence on decentralized clinical testing. Copenhagen 1986. Lancaster: MTP Press Limited, 1987:xv + 128 pp.
  • Bartola J. Physician office laboratory reim-bursement. Shifting strategies at the state level. Proceedings of the second annual insti-tute on clinical laboratory reimbursement policies. Arlington: Washington G-2 reports, 1984–09–07/08.
  • Beishon J, Peters G, eds. Systems behaviour. London: The Open University Press by Harper & Row, Publ., 1972:320 pp.
  • Belsey R, Baer D, Sewell D. Laboratory test analysis near the patient. Opportunities for improved clinical diagnosis and management. JAMA 1986;255:775–86.
  • Belsey RE, Baer DM, Statland BE, Sewell DL.The physician's office laboratory.Oradell: Medical Economics Books, 1986: 332 pp.
  • Belsey BE, Baer DM, Statland BE, Sewell DL.The physician's office laboratory.Oradell: Medical Economics Books, 1986:155–61.
  • BIPM, IEC, IFCC, ISO, IUPAC, OIML. International vocabulary of basic and general terms in metrology. Geneva: ISO, 1984: 40 pp. Amendments 1987 and Draft revision 1991, ISO/TAG 4/WG 1 N 77; 20 pp.
  • Bretherick L. Hazards in the chemical lab-oratory. 4th ed. London: Royal Society of Chemistry, 1986:604 pp.
  • British Standards Institution. Specification for microbiological safety cabinets. BS 5726. London: British Standards Institution, 1979: 16 pp.
  • British Standards Institution. Specifications for safety requirements for laboratory centri-fuges. BS 4402. London: British Standards Institution, 1982:16 pp.
  • British Standards Institution.Fire extin-guisher installation and equipment on prem-ises. Code of practice for the selection, in-stallation and maintenance of portable fire ex-tinguishers. BS 5306 Part 3. London: British Standards Institution, 1985: 24 pp.
  • Broughton PMG. Selection and maintenance of equipment. In: see ref no 122:157–61.
  • Broughton PMG, Buckley BM. Performance requirements of tests performed nearer the patient. Scand J Clin Lab Invest 1987;47: 99–104.
  • Broughton PMG, Herder M, Johansen KS, Magid E, eds. Laboratory medicine in pri-mary health care. A report on a joint WHO/NORDKEM/ECCLS workshop. Copenhagen (DK) 1988. Helsinki: Nordic Clinical Chemistry Project, 1989:35 pp.
  • Brown PA. Computers and communication. In: see ref no 122:131–8.
  • Browning DM. Premises and operational units. In: see ref no 4:43–7.
  • Browning DM, Cowell DC, Kilshaw D, Knowles D, Randall J, Singer R. Clinical chemistry equipment outside laboratories. Med Lab Sci 1984;41:99–107.
  • Clayton PD, Evans RS, Pryor T et al. Bring-ing HELP to the clinical laboratory - use of an expert system to provide automatic inter-pretation of laboratory data. Ann Clin Bio-chem 1987 ;24\(suppl 1):S1-5-S1–11.
  • Cotlove E, Harris EK, Williams GZ. Bio-logical and analytical components of variation in long-term studies of serum constituents in normal subjects. 3. Physiological and medi-cal implications. Clin Chem 1970;16: 1028–32.
  • Crawley R, Betsey R, Brock D & Baer DM. Regulation of physician's office laboratories. The Idaho experience.JAMA 1986;255:374–82.
  • Department of Health and Human Services (US), Food and Drug Administration. Good laboratory practice for nonclinical laboratory studies.Code of Federal Regulations 191987-04-01;title 21, part 58:228–42.
  • Department of Health and Human Services (US), Health Care Financing Administration. Medicare, Medicaid and CLIA programs. Regulations implementing the Clinical Labora-tory Improvement Amendments of 1988 (CLIA '88). Fed Reg 1990;55: 20895–959.
  • Department of Health, Education and Welfare (US), FDA. Nonclinical laboratory studies, good laboratory practice regulations. Fed Reg 1978;43:59986–60025.
  • Department of Health and Social Security. Code of practice for the prevention of infec-tion in clinical laboratories and post-mortem rooms. (The "Howie code of practice".) London: Department of Health and Social Security, 1978 (under revision):ix + 75 pp. Revised documents (added in the proofs):
  • a Health Services Advisory Committee. Safety in Health Service Laboratories; Safe working and the prevention of infection in clinical laboratories. London: Her Majesty's Station-ery Office, 1991:v+38 pp.
  • b Health Services Advisory Committee. Safety in Health Service Laboratories; Safe working and the prevention of infection in clinical laboratories - Model rules for staff and visi-tors. London: Her Majesty's Stationery Office, 1991:iii+ 11 pp.
  • Department of Health and Social Security (GB). Management of equipment. Health Equipment Information no 93. 1982:38 pp.
  • Department of Health and Social Security (GB). Code of practice for acceptance testing of electrically operated hospital laboratory equipment. Health Equipment Information no 140. 1985:39 pp.
  • Department of Health and Social Security (GB). Management budgetting in the National Health Service. London: Department of Health and Social Security, 1985:17 pp.
  • Department of Health and Social Security (GB). Electrical safety code for hospital laboratory equipment (ESCHLE). 2nd ed. Health Equipment Information no 158. 1986:38 pp.
  • Department of Health and Social Security (GB). Option appraisal; medical and scien-tific equipment: A guide for the National Health Service. London: Department of Health and Social Security, 1987:42 pp.
  • Department of Health and Social Security (GB). Health building note 15 - pathology department. London: Her Majesty's Statio-nery Office, in press.
  • Department of Health and Social Security, Advisory Committee on Dangerous Patho-gens. HIV - the causative agent of AIDS and related conditions. 2nd revision of guidelines. London: Department of Health and Social Security. 1990:57 pp.
  • Dybkaer R. Relations between hospital ward and laboratory. Z Med Lab Diagn 1984;25: 187–95.
  • Dybkaer R. The need for guidelines for decentralized clinical testing. In: see ref no 4:121–8.
  • Dybkaer R. Elements of good practice in decentralized clinical laboratories. In: see ref no 84:193–6.
  • Dybkaer R. Metrological problems and requirements in the life sciences. In: Kallner A, Bangham D, Moss D, eds. Improvement of comparability and compatibility of labora-tory assay results in life sciences. 1st Berg-meyer conference. Principles of assays in medical sciences.Bad Tölz, DE, 1988.Scand J Clin Lab Invest 1989;49\(suppl 193):104–7.
  • Dybkazr R, Jorgensen K. Measurement, value, and scale. Scand J Clin Lab Invest 1989;49\(suppl 194):69–76.
  • Dybkxr R, Jorgensen K. Quantities and units in clinical chemistry. Including recommenda-tion 1966 of the Commission on Clinical Chemistry of the International Union of Pure and Applied Chemistry and of the Interna-tional Federation for Clinical Chemistry. Copenhagen: Munksgaard, 1967:x + 102 pp.
  • EC. Commission directive of 1976-07-14. 76/907/EEC. Off J Eur Comm 1976:no L 360/1-18, 405–424.
  • EC. Commission directive of 1983-07-29. 83/467/EEC. Off J Eur Comm. 1983:no L 257/1–33.
  • EC.Council directive of 1986-12-18.87/18/EEC. Off J Eur Comm I987:no L 15/29–30.
  • EC.Council directive of 1988-06-09. 88/320/EEC. Off J Eur Comm 1988:no L 145/35–7.
  • ECCLS. Good manufacturing practice. Good clinical laboratory practice. The value of consultation between clinicians, surgeons and laboratory scientists. In: Gloag EA, ed. Proceedings of fourth ECCLS seminar. Beckenham, Kent: ECCLS, 1984:139 pp.
  • ECCLS. Standard for specimen collection. Part 1. Blood containers. ECCLS document 1(1);1984:6 pp.
  • ECCLS. Standard for quality assurance. Part 3. External quality assessment in microbiol-ogy. ECCLS document 2(2); 1985:14 pp.
  • ECCLS. Standard for the labelling of clinical laboratory materials. ECCLS document 1985; 2(3):10 pp.
  • ECCLS. Standard for quality assurance. Part 2. Internal quality control in microbiol-ogy. ECCLS document 2(4);1985: 22 pp.
  • ECCLS. Standard for quality assurance. Part 5. External quality assessment in haema-tology. ECCLS document 1986;3(1):11 pp.
  • ECCLS. Guidelines for the evaluation of analysers in clinical chemistry.ECCLSdocument 1986;3(2):32 pp.
  • ECCLS. Guidelines for a user laboratory to evaluate and select a kit for its own use. Part 1. Quantitative tests. ECCLS document 1986;3(3):17 pp.
  • ECCLS. Draft standard for specimen collec-tion. Part 3. Blood specimen by skin punc-ture. Draft ECCLS document 1986:13 pp.
  • ECCLS. Standard for specimen collection. Part 2. Blood specimen by venepuncture. ECCLS document 1987;4(1):11 pp.
  • ECCLS. Standard for quality assurance. Part 4. Internal quality control in haematology. ECCLS document 1987;4(2):13 pp.
  • ECCLS. Guidelines for the evaluation of diagnostic kits. Part 2. General principles and outline procedures for the evaluation of kits for qualitative tests. ECCLS document 1, 1990:38 pp.
  • ECCLS. Guidelines for the preparation of operation manuals for laboratory instruments. ECCLS document 3, 1990:13 pp.
  • ECCLS. Guidelines for protection of labora-tory workers from infectious agents trans-mitted by blood and other biological material. ECCLS document 4, 1990:67 pp.
  • ECCLS. Guidelines for the identification and distribution of patient samples in the medical laboratory. ECCLS document 5, 1990:38 pp.
  • Elevitch FR, ed. Proceedings of the 1976 Aspen conference on analytical goals in clini-cal chemistry. Chicago: College of American Pathologists, 1977:vi + 129 pp.
  • Elion-Gerritzen WE. Requirements for ana-lytical performance in clinical chemistry. An evaluation from the point of view of the prac-tising physician (Dissertation). Rotterdam: University of Rotterdam, 1978:103 pp.
  • Evans SE, Buckley BM. Biochemists nearer the patient? Br Med J 1983;287:1399.
  • Everett K, Hughes D. A guide to laboratory design. Butterworths, 1975.
  • Fabray CE. Methods of measuring work and costing activity in pathology departments. Dudley, Financial information project. Work-ing paper no 83/01. London: Department of Health and Social Security, 1983:34 pp.
  • Faulkner WR, Meites S. eds. Selected methods for the small clinical chemical lab-oratory. Washington, DC: AACC, 1982:395 pp. (Marcum VS, ed. Selected methods of clinical chemistry; vol 9.) 66Forrey AW, Delaney CJ, Ruff WL. Safety. In: Faulkner WR, Meites S. eds. Selected methods for the small clinical chemistry laboratory. Washington: American Associ-ation for Clinical Chemistry, 1982:330 pp.
  • Fraser CG. The application of theoretical goals based on biological variation data in proficiency testing. Arch Pathol Lab Med 1988;112:404–15.
  • Fraser CG, Geary TD. Guidelines for the performance of clinical biochemistry tests outside laboratories. Clin Biochem Revs (Australia) 1981;2:24–5.
  • Fraser CG, Watkinson LR. Patient, specimen and analysis as potential sources of error. In: see ref no 122:11–32.
  • Fraser CG, Wilde CE. The evaluation of a reagent kit for use in the clinical laboratory. Commun Lab Med 1985;1:80–2.
  • Fraser CG, Wilde CE. Statistical analysis of reagent kit evaluation data. Commun Lab Med 1986;2:1–5.
  • Fraser CG, Wilde CE. Criteria for the acceptability of a reagent kit. Commun Lab Med 1986;2:35–9.
  • Gilbert RK. Progress and analytical goals in clinical chemistry. Am J Clin Path 1975;63: 960–73.
  • Gillet GT. Clinical biochemistry nearer the patient II. Lancet 1986(ii):209–11.
  • Grayson RT. Effects of regulatory controls on the accuracy of clinical laboratory tests. J Med Tech 1984;1:632–7.
  • Groth T. Analytical quality, test quality and quality costs. Upsala J Med Sci 1986;91: 205–8.
  • Groth T, Larsson 0, Aronsson T, de Verdier C-H. Data base management systems for evaluation of analytical procedures. In: De Verdier C-H, Aronsson T, Nyberg A, eds. Quality control in clinical chemistry - Efforts to find an efficient strategy. The Nordic clinical chemistry project (NORDKEM). Scand J Clin Lab Invest 1984;44\(suppl 172):209–13.
  • Guder WG, Wahlefeld AW. Specimens and samples in clinical laboratory sciences. In: Bergmeyer HU, ed. Methods of enzyme analysis. 3rd ed. Vol. 2. Weinheim: Verlag Chemie, 1983:1–20.
  • Haeckel R. Cost implications of decentralizedtesting - a laboratorian's view. In: see ref no 4:109–17.
  • Haeckel R, Bonini P, Ceriotti G, Kutter D, Vonderschmitt DJ. Multi-centre evaluation of the urine test strip analyzer Rapimat. .J Clin Chem Clin Biochem 1985;23:473–92.
  • Harris EK. Statistical principles underlying analytical goalsetting in clinical chemistry. Am J Clin Path 1979;72:374–82.
  • Health and Safety Commission. Health and safety (first aid) regulations. Approved code of practice (guidance notes). London: Her Majesty's Stationery Office, 1990:30 pp.
  • Health and Safety Commission, Health Ser-vices Advisory Committee. Safety in health service laboratories: Hepatitis B. Bootle: Her Majesty's Stationery Office, 1985:iii + 8 pp.
  • Hellsing K, Berg B, Jagenburg R, Kallner A, von Schenk H, eds. Symposium on Analyti-cal systems near the patient. Proceedings of a Swedish Society for Clinical Chemistry Symposium. Uppsala (SE) 1985. Upsala Med Sci 1986;91:119–227.
  • HMSO. Safety in health service laboratories: the labelling, transport and reception of speci-mens. London: Her Majesty's Stationery Office, 1986:7 pp.
  • HMSO. Guidance notes for the protection of persons against ionising radiations arising from medical and dental use. London: Her Majesty's Stationery Office, 1988: 87 pp.
  • Horder M, ed. Assessing quality require-ments in clinical chemistry. The Nordic clinical chemistry project (NORDICEM). Scand J Clin Lab Invest 1980; 40 (suppl 155): 144 pp.
  • IFCC. The future small lab. IFCC News 1983(3):1–4 & 1984(1):2–5.
  • IFCC, Committee on Standards, Expert Panel on Nomenclature and Principles of Quality Control in Clinical Chemistry. Approved recommendation (1978). Quality control in clinical chemistry. Part 1. General principles and terminology. Clin Chim Acta 1979;98: 129F–43F.
  • IFCC, Committee on Standards, Expert Panel on Nomenclature and Principles of Quality Control in Clinical Chemistry. Approved recommendation (1978). Quality control in clinical chemistry. Part 2. Assessment of analytical methods for routine use. Cl in Chim Acta 1979;98:145F–62F.
  • IFCC, Education Committee. Guidelines (1985) for teaching of clinical chemistry to medical students. J Clin Chem Clin Biochem 1985;23:697–703.
  • IFCC, Education Committee. Definition of the terms certification, licensure and accredit-ation in clinical chemistry. J Clin Chem Clin Biochem 1985;23:899–901.
  • IFCC, Scientific Committee, Expert Group on Diagnostic Kits and Reagents. Revised rec-ommendation (1983). Evaluation of diagnos-tic kits. Part 1. Recommendations for spec-ifications on labelling of clinical laboratory materials. I Clin Chem Clin Biochem 1983;21:893–8.
  • IFCC, Scientific Committee, Expert Group on Diagnostic Kits and Reagents. Revised rec-ommendation (1983). Evaluation of diagnos-tic kits. Part 2. Guidelines for the evaluation of clinical chemistry kits. J Clin Chem Clin Biochem 1983;21:899–902.
  • IFCC, Scientific Committee, Expert Panel on Drug Effects. Drug interferences and drug effects in clinical chemistry. Part 7. Data banks. I Clin Chem Clin Biochem 1987;25: 191–4.
  • IFCC, Scientific Committee, Expert Panel on Nomenclature and Principles of Quality Con-trol in Clinical Chemistry. Approved recom-mendation (1979). Quality control in clinical chemistry. Part 3. Calibration and control materials. J Clin Chem Clin Biochem 1980; 18:855–60.
  • IFCC, Scientific Committee, Expert Panel on Nomenclature and Principles of Quality Con-trol in Clinical Chemistry. Approved recom-mendation (1979). Quality control in clinical chemistry. Part 6. Quality requirements from the point of view of health care. J Clin Chem Clin Biochem 1980;18:861–6.
  • IFCC, Scientific Committee, Expert Panel on Nomenclature and Principles of Quality Con-trol in Clinical Chemistry. Approved recom-mendation (1983). Quality control in clinical chemistry. Part 4. Internal quality control. J Clin Chem Clin Biochem 1983;21:877–84.
  • IFCC, Scientific Committee, Expert Panel on Nomenclature and Principles of Quality Con-trol in Clinical Chemistry. Approved recom-mendation (1983). Quality control in clinical chemistry. Part 5. External quality control. J Clin Chem Clin Biochem 1983;21:885–92.
  • IFCC, Scientific Committee, Expert Panel on Theory of Reference Values & ICSH, Stand-ing Committee on Reference Values. Approved Recommendation (1987). The the-ory of reference values. Part 6. Presentation of observed values related to reference values. J Clin Chem Clin Biochem 1987;25:657–62.
  • International Commission on Radiological Protection. Recommendations of ICRP - a summary. Publication no 26. Oxford: Perga-mon Press, 1977.
  • International Electrotechnical Commission. Safety requirements for electrical equipment for measurement, control and laboratory use. IEC 1010–1. Geneva: IEC, 1990:187 pp.
  • ISO. Statistics - vocabulary and symbols. Statistical quality control. ISO 3534. Geneva: ISO, 1977:47 pp.
  • ISO. Terms and definitions used in connec-tion with reference materials. ISO Guide 30. Geneva: ISO, 1981:5 pp.
  • ISO. Fire protection - vocabulary - Part 1. General terms and phenomena of tire. ISO 8421–1. Geneva: ISO, 1987:6 pp.
  • ISO. Fire protection - vocabulary - Part 2. Structural fire protection.ISO 8421–2.Geneva: ISO, 1987:4 pp.
  • IUPAC, Section of Clinical Chemistry, Com-mission on Quantities and Units in Clinical Chemistry & IFCC, Committee on Standards, Expert Panel on Quantities and Units. Approved recommendation (1978). Quantities and units in clinical chemistry. Clin Chim Acta 1979;96:157F–83F.
  • IUPAC, Section on Clinical Chemistry, Com-mission on Quantities and Units in Clinical Chemistry & IFCC, Committee on Standards, Expert Panel on Quantities and Units. Approved recommendation (1978). List of quantities and units in clinical chemistry. Clin Chim Acta 1979;96:185F–204F.
  • Kennedy ML. Laboratory performance and regulatory requirements. An empirical assess-ment of the quality assurance effects of selected regulatory requirements on the per-formance of clinical laboratories. Atlanta: Atlanta Centers for Disease Control, 1981: 34 pp.
  • Koepke JA. Evaluation and use of laboratory instrumentation for office haematology pro-cedures. In: Brown E, ed. Progress in hematology; vol 15. New York: Grune and Stratton, 1987:243–60.
  • Kutter D.Schnelltests in der klinischenDiagnostik. 2nd ed. Munich: Urban & Schwarzenberg, 1983:xii + 275 pp.
  • Kutter D. Quality assurance, teaching and training. In: see ref no 4:73–82.
  • Laboratory Standardization Panel of the National Cholesterol Education Program. Current status of blood cholesterol measure-ment in clinical laboratories in the United States. Clin Chem 1988;34:193–201.
  • Landaas S, Juell A. The quality of laboratory analyses in the primary health care. A profi-ciency survey on hemoglobin, glucose, leuco-cyte count and sedimentation rate (ESR) measurements. Scand J Prim Health Care 1986;4:169–73.
  • Lee HA. The renal unit. In: See ref no 122:184–9.
  • Leigh JM. Intensive care unit and operating theatre. In: see ref no 122:178–83.
  • Lewis SM. Quality assurance in haema-tology. WHO Lab/86.5. Geneva: WHO, 1986:56 pp.
  • Lewis SM. Training course in quality assur-ance. In: Lewis SM, Verwilghen RL, eds. Quality assurance in haematology. London: Bailliere Tindall, 1988:257–86.
  • Marks V. Clinical biochemistry nearer the patient. Brit Med J 1983;286:1166–7.
  • Marks V. Therapeutic drug monitoring. In: see ref no 122: 190–3.
  • Marks V. Essential considerations in the provision of near-patient testing facilities. Ann Clin Biochem 1988;25:220–5.
  • Marks V, Alberti KGMM, eds. Clinical bio-chemistry nearer the patient. Edinburgh: Churchill Livingstone, 1985:x + 240 pp. (Alberti KGMM, Galen RS, Marks V, eds. Contemporary issues in clinical chemistry; vol 2.)
  • Marks V, Alberti KGMM, eds. Clinical biochemistry nearer the patient II. London: Baillière Tindall, 1986:xii + 192 pp.
  • McMinn A, Russel GJ. Training of medical laboratory technicians: a handbook for tutors. Geneva: WHO, 1975:83 pp.
  • Mount IN, Slavin B. Bedside biochemistry. J Clin Pathol 1984;37:715.
  • NCCLS. Clinical laboratory procedure man-uals. Approved guideline GP2-A. NCCLS document 1984;4(2):vii + 27–53.
  • NCCLS. Clinical laboratory hazardous waste. Proposed guideline.NCCLS documentGP5-P. Draft 1986;6:44 pp.
  • NCCLS. Preliminary evaluation of clinical chemistry methods. Tentative guideline. NCCLS document EP1O-T. 1989;9(3):vii + 167–215.
  • NCCLS. Physician's office laboratory guide-lines. Tentative guidelines. NCCLS docu-ment POL I -T. 1989;9(4): ix + 224 pp. (Blood and urine collection, preparation, and transport 75–98).
  • NCCLS. Physician's office laboratory guide-lines. Method/instrument selection, evalu-ation and operation. Tentative guidelines. NCCLS document POL1-T. 1989;9 (4): 41–73.
  • NCCLS. Physician's office laboratory pro- cedure manual.Tentative guidelines.NCCLS document POL2-T. 1989;9(5):iii + 70 pp.
  • NCCLS. Protection of laboratory workers from infectious disease transmitted by blood, body fluids, and tissue. Tentative guideline. NCCLS document M29-1'2. 1991.
  • NCCLS. Protection of laboratory workers from instrument biohazards.Proposedguideline. NCCLS document I17-P. In press. viii + 45 pp.
  • Netter R. Cost implications of decentralized testing - a health agency's view. In: see ref no 4:105–8.
  • Ng RH. Selecting instrumentation for phys-icians office testing. In: see ref no 151.
  • NORDKEM. The role of clinical chemistry at the primary health care level. A report from a NORDKEM project (in press 1992).
  • OECD. Principles of good laboratory prac-tice. ENV/CHEM/MC/81.14. Manuscript, 1981:15–44.
  • OECD, Committee for the Final Report of the Working Group on Mutual Recognition of Compliance with Good Laboratory Practice. ENV/CHEM/CM/87.7. OECD Environment Monographs 1988\(no 15):29–35 & 41–54.
  • Pearce DN. Cost-benefit analysis. 2nd ed. London: MacMillan, 1983:112 pp.
  • Petersen PH, Rosleff F, Rasmussen J, Holbolth N. Studies on the required analyti-cal quality of ISH measurements in screening for congenital hypothyroidism. Scand J Clin Lab Invest 1980;40\(suppl 155):85–93.
  • Price CP. Quality assurance of extra-labora-tory analyses. In: see ref no 123:166–78.
  • Richardson JH, Emmett-Barkley W, eds. Biosafety in microbiological and biomedical laboratories. HHS publication (CDC) 86–8395. Washington: US Government Printing Office, 1984:149 pp.
  • Rock RC. Distributed technology: managing decentralised clinical biochemistry. In: see ref no 122:222–36
  • Rowan RM. Health and safety in labora-tories. In: See ref no 118:229–56.
  • Sandler G. Immediacy: speed of response from the point of view of the physician. In: see ref no 122:38–51.
  • Scott P. Data collection from and control of decentralized analysers. In: see ref no 123: 148–56.
  • Shuffstall RM, Hemmaplardh B. The hospital laboratory, modern concepts of management, operations and finance. St. Louis: The C V Mosby Company, 1979:xi + 208 pp.
  • Skendzel LP, Barnett RN, Platt R. Medically useful criteria for analytic performance of laboratory tests. Am J Clin Pathol 1985;83: 200–5.
  • Smith JH. Laboratory staff and nurse's performance compared when using the blood glucose Reflotest-Reflomat system. Med Lab Sci 1983;40:283–5.
  • Stamm D. Recommendations for the descrip-tiorl of a selected method in clinical chemis-try. J Clin Chem Clin Biochem 1979;17: 280–2.
  • Statland BE, Moskowitz MA, eds. Clinics in laboratory medicine; vol 6(2). Office practice in laboratory medicine. Philadelphia:WB Saunders Company, 1986;203–399.
  • Stranlcs J, Dewis M. Health and safety prac-tice. London: RoSPA pub. Pitman, 1986: 169–77.
  • Thomas L. Neue Entwicklungen und Tech-niken auf dem Gebiet der Präsenzdiagnostik. Lab Med 1986;10:153–9.
  • Tonics DB. A study of the accuracy and precision of clinical chemistry determinations in 170 Canadian laboratories. Clin Chem 1963;9:217–23.
  • Tryding N. Education and training of clinical chemistry in primary health care. In: Herder M, Knudsen L, Hyltoft Petersen, P, eds. Nordic clinical chemistry. Current trends. Transactions of the 20th Nordic congress in clinical chemistry. Odense, DK, 1986. Scand J Clin Lab Invest 1986;46\(suppl 185): 51.
  • Tryding N. Clinical need for analyses nearer the patient. Upsala J Med Sci 1986;91:185–8.
  • Uldall A. Quality assurance in clinical chem-istry. Scand J Clin Lab Invest 1987;47\(suppl 187):5–94.
  • Wahba WA. Technician and technologist training in clinical chemistry. In: Kaiser E, Gabl F, Mueller MM, Bayer PM, eds. Pro-ceedings of the eleventh international congress of clinical chemistry. Vienna 1981. Berlin: Walter de Gruyter, 1982:79–89.
  • Westgard JO, Barry PL.Cost-effectivequality control: Managing the quality control and the productivity of analytical processes. Washington: AACC Press, 1986:92–117.
  • Westgard JO, Barry PL, Groth T. Workshop for teaching quality control to laboratory personnel: objectives and guidelines. Scand J Clin Lab Invest 1984;44\(suppl 172):215–8.
  • Westgard JO, Barry PL, Hunt MR, Groth T. Proposed selected method. A multi-rule Shewhart chart for quality control in clinical chemistry. Clin Chem 1981;27:493–501.
  • Westgard JO, Groth T, Aronsson T, Falk H, de Verdier C-H. Performance characteristics of rules for internal quality control: Probabil-ities for false rejection and error detection. Clin Chem 1977;23:1857–67.
  • Westgard JO, Groth T, de Verdier C-H. Principles for developing improved quality control procedures. In: De Verdier C-H, Aronsson T, Nyberg A, eds. Quality control in clinical chemistry - Efforts to find an efficient strategy. The Nordic clinical chem-istry project (NORDKEM). Scand J Clin Lab Invest 1984;44\(suppl 172):19–41.
  • Whitehead TP. Quality control in clinical chemistry. New York: John Wiley, 1977: 144 pp.
  • WHO. Guiding principles and recommen-dations on labelling of clinical laboratory materials (1978). WHO memorandum. Bull WHO 1978;56:881–5.
  • WHO. Task force on the development of appropriate technology for health in the field of laboratory equipment, Geneva 1979. WHO/ATH/79.2. Geneva: WHO, 1979: 22 pp.
  • WHO. Self-instruction sheets for users of primary health care laboratory equipment. WHO/LAB/85.7. Geneva: WHO, 1985:34 pp.
  • WHO. Laboratory services at the primary health care level. WHO/LAB/87.2. Geneva: WHO, 1987:31 pp.
  • WHO. Self-instruction sheets for users of laboratory instruments in intermediate hospital laboratories. WHO/LAB/87.3. Geneva: WHO, 1987:15 pp.
  • WHO, Regional Office for Europe. Targets for health for all. Targets in support of the European regional strategy for health for all. Copenhagen: WHO/EURO 1986:xiv + 201 pp.
  • WHO, Regional Office for Europe. Health surveillance and training programmes for biomedical laboratory staff and support staff. Biological safety. Manuscript. Copenhagen: WHO/EURO 1989:5 pp.
  • WHO, Regional Office for Europe, ECCLS. Guidelines on good practice in clinical labora-tories. I. Clinical chemistry. Copenhagen: WHO/EURO, ECCLS 1991:29 pp.
  • WHO, Working Group on Assessment of Clinical Technologies.Identification ofessential clinical chemical and haematological tests in intermediate hospital laboratories. WHO/LAB/86.2. Geneva: WHO, 1986:12 pp.
  • WHO, Working Group on Assessment of Clinical Technologies.Methods recom-mended for essential clinical chemical and haematological tests for intermediate hospital laboratories. WHO/LAB/86.3. Geneva: WHO, 1986:127 pp.
  • Wilde CE. The selection of reagent kit for regular use in the clinical laboratory. Cornmun Lab Med 1985;1:5–7.
  • Wilde CE. Introduction of reagent kit into regular use in the clinical laboratory. Commun Lab Med 1986;2:71–5.
  • Wilde CE. Patient reception, preparation, specimen handling and data flow. In: see no 4:63–72.

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