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8.    Without prejudice to the foregoing if injury is suffered by a Subject while participating in the
                 Study, the Sponsor agrees to operate in good faith the Guidelines published in 1991 by The
                 Association of the British Pharmaceutical Industry and entitled “Clinical Trial Compensation
                 Guidelines” (where the Subject is a patient) and the Guidelines published in 1988 by the same
                 Association and entitled “Guidelines for Medical Experiments in non-patient Human
                 Volunteers” (where the Subject is not a patient) and shall request the Investigator to make clear
                 to the Subjects that the Study is being conducted subject to the applicable Association
                 Guidelines.

           9.    For the purpose of this indemnity, the expression “agents” shall be deemed to include without
                 limitation any nurse or other health professional providing services to the Authority under a
                 contract for services or otherwise and any person carrying out work for the Authority under such
                 a contract connected with such of the Authority’s facilities and equipment as are made available
                 for the Study under paragraph 2 above.

           10.   This indemnity shall be governed by and construed in accordance with English/Scottish* law.





           SIGNED on behalf of the Health Authority!
           Health Board/NHS Trust                      ........................................................................
                                                                             Chief Executive/
                                                                      District General Manager








           SIGNED on behalf of the Company









                                                      Dated












           *     Delete as appropriate
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