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Section 8 of the Regulation then prescribes, in part: The following are prescribed as matters for a head to consider in deciding whether to waive all or part of a payment required to be made under the Act 1 In this appeal, the Ministry agreed to disclose 72 pages of the hundreds of responsive records. Under section 57 5 ; , an appellant has the right to ask the Commissioner to review an institution's decision not to waive the fee. The Commissioner may then either confirm or overturn this decision based on a consideration of the criteria set out in section 57 4 ; of the Act Order P-474 ; . Many previous orders have held that the onus is on the appellant to demonstrate that a fee waiver would be justified. Orders M-429, M-598 and M-914 ; . I also conscious of the Legislature's intention to include a user pay principle in the Act, as evidenced by the provisions of section 57. The appellant submits that he is entitled to a fee waiver on the basis that "the outcome of this issue effects sic ; the public and drug prices the public pays and the issues from records received should be disseminated and reported to the public". However, the appellant provides no evidence or further elaboration in support. In its representations, the Ministry submits that the general public will not benefit from the dissemination of the information in the records since the majority of the people in Ontario are not users of the drugs that are the subject of the records. The appellant, in his reply, provided no evidence to refute the Ministry's statement. I satisfied that the subject matter of the requested records, the interchangeability of drugs, is a matter of public rather than private interest and related directly to a public health or safety issue. However, I not convinced that dissemination of the record would yield a public benefit by either disclosing a public health or safety concern or contributing meaningfully to the development or understanding of an important health or safety issue. I accept the Ministry's position that dissemination of the record will not provide a substantial benefit to public health and safety since the pool of potential beneficiaries is small. I further find it unlikely that the Whether the person requesting access to the record is given access to it and
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Chicago, Illinois PRWEB ; August 27, 2007 - People who have suffered for years from degenerative discs in their neck now have an option that may relieve the pain in their neck and arm, allow quick recovery and enable them to lead active and productive lives. On July 17, the Food and Drug Administration FDA ; cleared the Prestige ST Cervical Disc System. Used extensively in Europe, FDA clearance of the Prestige disc from Medtronic follows a unanimous recommendation for approval from the FDA advisory board. The artificial disc for the cervical neck ; region is expected to impact more than 200, 000 Americans who suffer from degenerative disc disease. Currently, the most common treatment for patients with degenerative discs in the cervical spine is spinal fusion. In this procedure a surgeon removes the damaged disc then implants a bone graft and metal plate to fuse the vertebrae together. During artificial disc replacement surgery, the damaged disc is removed and replaced with an artificial disc, a stainless-steel device with a ball-in-trough design intended to allow for replication of normal motion. The disc stays in place with bone screws. The hospital stay for this procedure is approximately 1-2 days. Patients can begin rehabilitation and return to daily activities soon after surgery. In fact, patients receiving the Prestige ST artificial disc returned to work in 45 days, 16 days earlier than the fusion patients. "Compared to spinal fusion, this surgery allows patients to maintain normal neck motion, and study has shown a lower rate of additional surgery for degeneration of adjacent segments, " says Noam Stadlan, M.D., CINN neurosurgeon CINN ; . "Unlike with fusion, patients who've received the disc don't have to bother with a hard collar following surgery." "Study results show that artificial cervical disc patients regain function faster, and have a higher rate of neurological success as measured by muscle tone, strength, sensation, as well as responsiveness of reflexes than those who undergo spinal fusion, " says Dr. Dean Karahalios, CINN neurosurgeon. "Furthermore, the study demonstrated that at two year follow-up the overall success rate for the artificial disc group was 79.3% compared to the fusion group at 67.8%. These reasons are compelling enough for potential candidates to consider the option of an artificial disc." The Chicago Institute of Neurosurgery and Neuroresearch is one of the nation's leading organizations for the diagnosis, treatment and rehabilitation of people with brain and spine disorders. Originally founded in 1987, CINN is one of the Midwest's largest teams of neurosurgeons, physiatrists and neurologists known for their pioneering treatments in minimally invasive techniques. Through a network of seven hospitals throughout Chicagoland, CINN is a market leader in treating patients with brain tumors and spine disorders. For more information on the cervical artificial disc, call: 1-800-446-1234 or visit cinn and sinequan.
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1. In recognition that problems affecting the global environment are serious matters for all mankind, harmony with the environment will be a top management priority throughout the Company. 2. By establishing a structure for the promotion of environmental protection, enacting regulations relating to the environment, setting environmental impact reduction targets and similar measures, officers and site directors in charge of environmental promotion will promote environmental preservation activities. Moreover, environmental audits will be used to confirm the efficacy of activities and in efforts for continued improvement. 3. By accurately understanding how best to resolve environmental problems facing the world, the Company will work to make contributions to society through the development of highly reliable technologies and products that meet those needs. 4. The Company gives due consideration to reducing the effect on the environment a product will have throughout its entire life cycle, from R&D and design stages through production, logistics, use and disposal. 5. The Company will investigate and examine the effect of its business operations on the environment and seek to introduce new technologies and materials with superior functionality regarding environmental safety, energy conservation and resource conservation. 6. In addition to observing international, national and local regulations with regard to the environment, the Company will develop its own standards where necessary to maintain environmental conservation. 7. With regard to overseas activities and the export of products, the Company will give consideration to the effects on the local environment and implement measures in response to the wishes of the local society. 8. In addition to working to enhance the environmental awareness of its employees, the Company will focus such activities on society at large, contributing to the society, of which Hitachi is a part, with environmental protection activities from a broad perspective. 9. Should an environmental problem arise as a result of the Company's business activities, the Company will take appropriate steps to minimize the impact on the environment.
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