Terms of agreement Pharmaceutical Society of Australia Sample Clauses

Terms of agreement Pharmaceutical Society of Australia. April 26th, 2018 - This sample contract has been provided as part of the Pharmaceutical Society of Australia Guidelines for Pharmacists The Provision of Pharmacy Services to Residential Aged Care Facilities November 2001'
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Terms of agreement Pharmaceutical Society of Australia. April 26th, 2018 - This sample contract has been provided as part of the Pharmaceutical Society of Australia Guidelines for Pharmacists The Provision of Pharmacy Services to Residential Aged Care Facilities November 2001' 'Independent Nurse Contractor Discover Nursing May 8th, 2018 - You’ll work on a contract basis providing care for those most in need You can be self employed or work with an agency Independent Nurse Contractor' 'Contract No PROFESSIONAL SERVICES AGREEMENT May 7th, 2018 - Page 1 Sample Contract Contract No PROFESSIONAL SERVICES AGREEMENT THIS AGREEMENT made and entered into this day of 20 by and between the SANTA' 'guidance on the nhs standard contract for care home april 21st, 2011 - this document is the guidance on the nhs standard contract for care home services 2011 12 to be read be in conjunction with the nhs standard contract for care homes' 'Core Set for PACE CRSP National PACE Association April 27th, 2018 - SAMPLE PROVIDER CONTRACT FOR NURSING HOME SERVICES CRSP Core Resource Set for PACE 000 Xxxxx Xxxxxxx Xxxxxx • Suite 309 • Alexandria Virginia 22314 Phone 000 000 0000 • Fax 000 000 0000 • www NPAonline org' 'HEALTH CARE SERVICE PROVIDER AGREEMENT May 8th, 2018 - HEALTH CARE SERVICE PROVIDER AGREEMENT Hereinafter Referred To As Provider A Physician Group Of Physicians Or Similar Provider Of Health Care Services Or''service agreement new era support services may 8th, 2018 - page 2 of 3 5 rates fees amp deposits agency will provide the services at the rates set out in the attached rate sheet 6 billing payment and overdue accounts' 'CONTRACT TEMPLATES LHIN HOME AND COMMUNITY CARE MAY 5TH, 2018 - CONTRACT TEMPLATES CURRENT SERVICE PROVIDERS ARE REQUIRED TO COMPLY WITH CURRENT OUR TERMS CONDITIONS AND SCHEDULES WE UPDATE OUR CONTRACTS AS NEEDED IN CONSULTATION WITH SERVICE PROVIDER STAKEHOLDERS AND MAKE THEM AVAILABLE HERE' 'NETWORK PROVIDER NURSE PRACTITIONER CONTRACT MAY 8TH, 2018 - NETWORK PROVIDER NURSE PRACTITIONER CONTRACT 2 6 HOSPITAL SERVICES MEANS THOSE ACUTE CARE INPATIENT AND OUTPATIENT HOSPITAL SERVICES THAT ARE''how to prepare an agreement to care for a family member march 7th, 2018 - the purposes of a written personal care agreement and what personal services agreement assistance for in home care the 'Sample Contract for Consulting Services thebalancesmb com 'service agreement contract amity in home care services inc may 6th, 2018 - service agreement contract amity in home care services inc rates are object to change upo...
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Terms of agreement Pharmaceutical Society of Australia. April 26th, 2018 - This Sample Contract Has Been Provided As Part Of The Pharmaceutical Society Of Australia Guidelines For Pharmacists The Provision Of Pharmacy Services To Residential Aged Care Facilities November 2001' 'reviewing the nursing home contract caregivers library may 6th, 2018 - reviewing the nursing home contract before your loved one signs a nursing home contract of health and human services health care financing''Sample Contract For Nursing Services pdfsdocuments2 com May 4th, 2018 - Sample Contract For Nursing Services pdf Free Download Here CONTRACTUAL AGREEMENT Skilled Nursing Services http www a1premierhca com contractual 20agreement 20skilled 20nursing 20services pdf' 'Sample Contract for Professional Service Businesses May 8th, 2018 - Here s a contract template you can use to create a personalized service contract It works well for any business that sells professional services''PERSONAL CARE AGREEMENTS A MUST FOR CAREGIVER 'SERVICE AGREEMENT NEW ERA SUPPORT SERVICES MAY 8TH, 2018 - PAGE 2 OF 3 5 RATES FEES AMP DEPOSITS AGENCY WILL PROVIDE THE SERVICES AT THE RATES SET OUT IN THE ATTACHED RATE SHEET 6 BILLING PAYMENT AND OVERDUE ACCOUNTS' 'TEMPORARY STAFFING AGREEMENT
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Terms of agreement Pharmaceutical Society of Australia. April 26th, 2018 - This Sample Contract Has Been Provided As Part Of The Pharmaceutical Society Of Australia Guidelines For Pharmacists The Provision Of Pharmacy Services To Residential Aged Care Facilities November 2001''guide to admission agreements for residential care may 6th, 2018 - guide to admission agreements for residential care admission agreements for residential care third party services a the agreement must' 'Guidance on the NHS Standard Contract for Care Home April 21st, 2011 - This document is the Guidance on the NHS Standard Contract for Care Home Services 2011 12 to be read be in conjunction with the NHS Standard Contract for Care Homes'
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Terms of agreement Pharmaceutical Society of Australia. APRIL 26TH, 2018 - THIS SAMPLE CONTRACT HAS BEEN PROVIDED AS PART OF THE PHARMACEUTICAL SOCIETY OF AUSTRALIA GUIDELINES FOR PHARMACISTS THE PROVISION OF PHARMACY SERVICES TO RESIDENTIAL AGED CARE FACILITIES NOVEMBER 2001' May 5th, 2018 - This basic four page contract form is a general agreement for staffing services General Staffing Agreement 6 Exhibit B Sample Benefits Waiver for Assigned Employees' MAY 2ND, 2018 - CREATE YOUR OWN CUSTOM VERSION OF THIS SENIOR HOME CARE SAMPLE PROPOSAL IN 5 STEPS OF A SENIOR HOME CARE SERVICES PROPOSAL AND CONTRACT'
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Terms of agreement Pharmaceutical Society of Australia. April 26th, 2018 - This Sample Contract Has Been Provided As Part Of The Pharmaceutical Society Of Australia Guidelines For Pharmacists The Provision Of Pharmacy Services To Residential Aged Care Facilities November 2001' 'NETWORK PROVIDER HOME HEALTH CARE AGENCY CONTRACT MAY 7TH, 2018 - 1 NETWORK PROVIDER HOME HEALTH CARE AGENCY CONTRACT IT IS HEREBY AGREED BETWEEN THE OFFICE OF MANAGEMENT AND ENTERPRISE SERVICES EMPLOYEES GROUP INSURANCE''General Staffing Agreement May 5th, 2018 - This basic four page contract form is a general agreement for staffing services General Staffing Agreement 6 Exhibit B Sample Benefits Waiver for Assigned Employees'
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Terms of agreement Pharmaceutical Society of Australia. Client Service Agreement
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Related to Terms of agreement Pharmaceutical Society of Australia

  • Tests and Preclinical and Clinical Trials The preclinical studies and clinical trials conducted by or, to the Company’s knowledge, on behalf of the Company, that are described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, as applicable, and are intended to be submitted to the U.S. Food and Drug Administration (the “FDA”) or other comparable government entities, were and, if still ongoing, are being conducted in all material respects in accordance with experimental protocols, procedures and controls pursuant to accepted professional scientific standards and all Authorizations and Applicable Laws, including, without limitation, current Good Clinical Practices and Good Laboratory Practices and any applicable rules and regulations of the jurisdiction in which such trials and studies are being conducted; the descriptions of the results of such studies and trials contained in the Registration Statement, the Pricing Disclosure Package and the Prospectus are, to the Company’s knowledge, accurate and complete in all material respects and fairly present the data derived from such studies and trials; except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package and the Prospectus, the Company is not aware of any studies or trials, the results of which the Company believes reasonably call into question the study or trial results described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus when viewed in the context in which such results are described and the clinical stage of development; and, except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package or the Prospectus, the Company has not received any written notices or written correspondence from the FDA or any governmental entity requiring the termination or suspension of any preclinical studies or clinical trials conducted by or on behalf of the Company, other than ordinary course communications with respect to modifications in connection with the design and implementation of such trials, copies of which communications have been made available to you.

  • Publicity; Terms of Agreement (a) The Parties agree that the material terms of this Agreement are the Confidential Information of both Parties, subject to the special authorized disclosure provisions set forth in Section 12.2 and this Section 12.3. The Parties have agreed to make a joint public announcement of the execution of this Agreement substantially in the form of the press release attached as Exhibit F on or after the Effective Date. (b) After issuance of such joint press release, if either Party desires to make a public announcement concerning the material terms of this Agreement, such Party shall give reasonable prior advance notice of the proposed text of such announcement to the other Party for its prior review and approval (except as otherwise provided herein), such approval not to be unreasonably withheld, except that in the case of a press release or governmental filing required by Applicable Law (where reasonably advised by the disclosing Party’s counsel), the disclosing Party shall provide the other Party with such advance notice as it reasonably can and shall not be required to obtain approval therefor. A Party commenting on such a proposed press release shall provide its comments, if any, within five (5) Business Days (or within three (3) Business Days in the event that Ambrx (or its Affiliate) is a public reporting company) after receiving the press release for review and the other Party shall give good faith consideration to same. Ambrx shall have the right to make a press release announcing the achievement of each milestone under this Agreement as it is achieved, and the achievements of Regulatory Approvals as they occur, subject only to the review procedure set forth in the preceding sentence. In relation to BMS’ review of such an announcement, BMS may make specific, reasonable comments on such proposed press release within the prescribed time for commentary, but shall not withhold its consent to disclosure of the information that the relevant milestone or Regulatory Approval has been achieved and triggered a payment hereunder. Neither Party shall be required to seek the permission of the other Party to repeat any information regarding the terms of this Agreement that have previously been publicly disclosed by such Party, or by the other Party, in accordance with this Section 12.3. For clarity, neither Party shall disclose the financial terms of this Agreement without the prior written approval of the other Party, except as and to the extent otherwise expressly permitted under this Agreement. (c) The Parties acknowledge that either or both Parties may be obligated to file under Applicable Law a copy of this Agreement with the SEC or other Government Authorities. Each Party shall be entitled to make such a required filing, provided that it requests confidential treatment of at least the financial terms and sensitive technical terms hereof and thereof to the extent such confidential treatment is reasonably available to such Party. In the event of any such filing, each Party will provide the other Party with a copy of this Agreement marked to show provisions for which such Party intends to seek confidential treatment not less than five (5) Business Days prior to such filing (and any revisions to such portions of the proposed filing a reasonable time prior to the filing thereof), and shall reasonably consider the other Party’s comments thereon to the extent consistent with the legal requirements, with respect to the filing Party, governing disclosure of material agreements and material information that must be publicly filed, and shall only disclose Confidential Information which it is advised by counsel or the applicable Governmental Authority is legally required to be disclosed. No such notice shall be required under this Section 12.3(c) if the substance of the description of or reference to this Agreement contained in the proposed filing has been included in any previous filing made by either Party hereunder or otherwise approved by the other Party. (d) Each Party shall require each of its Affiliates and private investors to which Confidential Information of the other Party is disclosed as permitted hereunder to comply with the covenants and restrictions set forth in Sections 12.1 through Section 12.3 as if each such Affiliate and each such investor were a Party to this Agreement and shall be fully responsible for any breach of such covenants and restrictions by any such Affiliate or investor.

  • International Olympic Committee; International Red Cross and Red Crescent Movement As instructed from time to time by ICANN, the names (including their IDN variants, where applicable) relating to the International Olympic Committee, International Red Cross and Red Crescent Movement listed at xxxx://xxx.xxxxx.xxx/en/resources/registries/reserved shall be withheld from registration or allocated to Registry Operator at the second level within the TLD. Additional International Olympic Committee, International Red Cross and Red Crescent Movement names (including their IDN variants) may be added to the list upon ten (10) calendar days notice from ICANN to Registry Operator. Such names may not be activated in the DNS, and may not be released for registration to any person or entity other than Registry Operator. Upon conclusion of Registry Operator’s designation as operator of the registry for the TLD, all such names withheld from registration or allocated to Registry Operator shall be transferred as specified by ICANN. Registry Operator may self-­‐allocate and renew such names without use of an ICANN accredited registrar, which will not be considered Transactions for purposes of Section 6.1 of the Agreement.

  • Quality Agreement Concurrently with execution of this Agreement, the Parties will enter into an agreement that details the quality assurance obligations of each Party with respect to the Manufacture and supply of Supplied Products under this Agreement (the “Quality Agreement”). Each Party shall perform its obligations under the Quality Agreement in accordance with the terms and conditions thereof. In the event of a conflict between the terms of the Quality Agreement and the terms of this Agreement, the provisions of the Quality Agreement shall govern.

  • Protocol The attached Protocol shall be an integral part of this Agreement.

  • Placement of DNS probes Probes for measuring DNS parameters shall be placed as near as possible to the DNS resolvers on the networks with the most users across the different geographic regions; care shall be taken not to deploy probes behind high propagation-­‐delay links, such as satellite links.

  • Copy of Agreement The Executive hereby acknowledges receipt of a copy of this Agreement duly signed by the Company.

  • ENHANCED AND SUPPLEMENTAL SERVICES BY COUNTY 8 1. Enhanced services for events on CITY property. At the request of CITY, 9 through its City Manager, SHERIFF may provide enhanced law enforcement 10 services for functions, such as community events, conducted on property 11 that is owned, leased or operated by CITY. SHERIFF shall determine 12 personnel and equipment needed for such enhanced services. To the 13 extent the services provided at such events are at a level greater than that 14 specified in Attachment A of this Agreement, CITY shall reimburse COUNTY 15 for such additional services, at an amount computed by SHERIFF, based on 16 the current year’s COUNTY law enforcement cost study. The cost of these 17 enhanced services shall be in addition to the Maximum Obligation of CITY 18 set forth in Subsection G-2 of this Agreement. SHERIFF shall xxxx CITY 19 immediately after each such event. 20 2. Supplemental services for occasional events operated by private

  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMEA, Health Canada and other comparable drug and medical device (including diagnostic product) regulatory agencies outside of the United States to which they are subject; the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Disclosure Package and the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement, the Time of Sale Disclosure Package or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMEA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.

  • Pharmacovigilance Agreement Subject to the terms of this Agreement, and at a date to be determined by the JDC, Facet and Trubion shall define and finalize the actions the Parties shall employ to protect patients and promote their well-being in a written agreement (hereinafter referred to as the “Pharmacovigilance Agreement”). These responsibilities shall include mutually acceptable guidelines and procedures for the receipt, investigation, recordation, communication, and exchange (as between the Parties) of adverse event reports, pregnancy reports, and any other information concerning the safety of any Collaboration Product. Such guidelines and procedures shall be in accordance with, and enable the Parties to fulfill, local and national regulatory reporting obligations to Governmental Authorities. Furthermore, such agreed procedures shall be consistent with relevant ICH guidelines, except where said guidelines may conflict with existing local regulatory safety reporting requirements, in which case local reporting requirements shall prevail. The Pharmacovigilance Agreement will provide for a worldwide safety database to be maintained by the Party appointed by the JDC. Each Party hereby agrees to comply with its respective obligations under such Pharmacovigilance Agreement (as the Parties may agree to modify it from time to time) and to cause its Affiliates and permitted sublicensees to comply with such obligations.

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