The Clinic Sample Clauses

The Clinic. CompBioMed will target the clinical stakeholders, including health care professionals such as doctors and surgeons. We expect that computational modelling of the human body and physiology will impact the field of biomedicine by fundamentally altering the basis for the diagnosis and treatment of disease into a personalised, predictive, participatory and preventative process. In the future, medical innovation will be directed towards optimising treatments using integrated functional simulation in silico, assembling a customised computer model of a patient's condition across multiple organ systems and length scales (from molecular to human to population), across timescales from nanoseconds to years, and allowing for the influence of the environment. The quality and usability of our software will put us in an influential position in terms of promoting modelling and associated software standards internationally. The presence of clinical partners within our consortium will ensure that we exploit any potential impact of these modelling tools in a clinical context. Through integration into clinical decision support systems, computer based modelling and simulation will be able to advise courses of action ahead of treatments, including interventions, which will lead to improved outcomes for patients and enhance the health and wellbeing of the European Union. An important impact of the in silico technologies we are promoting will be to reduce, refine and eventually replace animal experimentation in biomedical research, putting simulation on an equal footing with sequencing and imaging. Various computational biomedicine projects that have developed advanced technologies are struggling to move to clinical trials phases because the technological expertise is lacking from many research hospitals. However, once any one of these computational workflows is established and put in use in a clinical setting, it is possible to amass hundreds of patient-specific simulations. Even if the primary data had to be destroyed on grounds of privacy, these data can be used to identify input parameter distributions that characterise well in silico populations, with respect to the particular pathophysiological process captured by the simulation. If these data can be combined with a simulation of an intervention, what we obtain are so-called ‘in silico clinical trials’, wherein a new surgical procedure, the insertion of a new medical device, or the assumption of a new drug is simulated with...
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The Clinic. The Corporation is duly authorized to operate the Clinic under California law as an outpatient rehabilitation clinic. The Personal Property is all of the property necessary for the lawful operation of the Clinic at its current level of business.
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The Clinic 
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Related to The Clinic

  • Medi Cal PII is information directly obtained in the course of performing an administrative function on behalf of Medi-Cal, such as determining Medi-Cal eligibility or conducting IHSS operations, that can be used alone, or in conjunction with any other information, to identify a specific individual. PII includes any information that can be used to search for or identify individuals, or can be used to access their files, such as name, social security number, date of birth, driver’s license number or identification number. PII may be electronic or paper. AGREEMENTS

  • Manufacturing and Marketing Rights The Company has not granted rights to manufacture, produce, assemble, license, market, or sell its products to any other person and is not bound by any agreement that affects the Company's exclusive right to develop, manufacture, assemble, distribute, market, or sell its products.

  • Training and Education SECTION 1 – Law Enforcement Supervisors’ Training The state and the PBA recognize the importance of supervisor training programs to develop management skills in our law enforcement supervisors. The state will make a reasonable effort to continue existing training programs in law enforcement techniques and to develop new programs in performance review techniques, supervisory skills, and managerial techniques.

  • Manufacturing Technology Transfer With respect to each Technology Transfer Product, upon AbbVie’s written request after the Inclusion Date for the Included Target to which such Technology Transfer Product is Directed, Morphic shall effect a full transfer to AbbVie or its designee (which designee may be an Affiliate or a Third Party manufacturer) of all Morphic Know-How and Joint Know-How relating to the then-current process for the Manufacture of such Technology Transfer Product (the “Manufacturing Process”) and to implement the Manufacturing Process at facilities designated by AbbVie (such transfer and implementation, as more fully described in this Section 5.3, the “Manufacturing Technology Transfer”). To assist with the Manufacturing Technology Transfer, Morphic will make its personnel reasonably available to AbbVie during normal business hours for up to [***] FTE hours with respect to each Included Target (in each case, free of charge to AbbVie) to transfer and implement the Manufacturing Process under this Section 5.3. Thereafter, if requested by AbbVie, Morphic shall continue to perform such obligations; provided, that AbbVie will reimburse Morphic for its full-time equivalent (FTE) costs (for clarity, in excess of [***] FTE hours) and any reasonable and verifiable out-of-pocket costs incurred in providing such assistance. CERTAIN CONFIDENTIAL INFORMATION CONTAINED IN THIS DOCUMENT, MARKED BY [***], HAS BEEN OMITTED BECAUSE IT IS NOT MATERIAL AND WOULD LIKELY CAUSE COMPETITIVE HARM TO THE COMPANY IF PUBLICLY DISCLOSED.

  • Manufacturing and Supply Genentech shall be responsible for manufacturing and supplying Licensed Products for clinical use and commercial sale in the Genentech Field.

  • Compliance Program The Company has established and administers a compliance program applicable to the Company, to assist the Company and the directors, officers and employees of the Company in complying with applicable regulatory guidelines (including, without limitation, those administered by the FDA, the EMA, and any other foreign, federal, state or local governmental or regulatory authority performing functions similar to those performed by the FDA or EMA); except where such noncompliance would not reasonably be expected to have a Material Adverse Effect.

  • Quality Assurance The parties endorse the underlying principles of the Company’s Quality Management System, which seeks to ensure that its services are provided in a manner which best conforms to the requirements of the contract with its customer. This requires the Company to establish and maintain, implement, train and continuously improve its procedures and processes, and the employees to follow the procedures, document their compliance and participate in the improvement process. In particular, this will require employees to regularly and reliably fill out documentation and checklists to signify that work has been carried out in accordance with the customer’s specific requirements. Where necessary, training will be provided in these activities.

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time.

  • Information Technology The following applies to all contracts for information technology commodities and contractual services. “Information technology” is defined in section 287.012(15), F.S., to have the same meaning as provided in section 282.0041, F.S.

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