Quality and Safety Reporting Sample Clauses

Quality and Safety Reporting. Biochrom shall maintain a documented reporting system to GE Healthcare when Biochrom has knowledge of any product issue related to safety or quality, which results in the stopping of a shipment or a Product recall. Any actions taken by Biochrom to report a recall to a regulated agency must be communicated to GE Healthcare within twenty-four (24) hours. GE Healthcare has the right to request Biochrom to provide all documents regarding the specific issue including the analysis, root cause and corrective action taken to minimize any risk to GE Healthcare customers.
Sample 1
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Quality and Safety Reporting. The Supplier shall maintain a documented reporting system to GE Healthcare when the Supplier has knowledge of any product issue related to safety or quality that results in stopping shipment or requires a recall. Any actions taken by the Supplier to report a recall to a regulated agency must be communicated to GE Healthcare immediately (within 3 business days). GE Healthcare has the right to request Supplier to provide all documents regarding the specific issue including the analysis, root cause and corrective action taken to minimize any risk to GE Healthcare customers. By signing below, you agree to the terms hereof and consent to meet all requirements that apply for any and all products and services provided to GE Healthcare. Agreed to and Accepted by Supplier Signature: Printed Name: Title: Date: Supplier Name: Agreed to and Accepted by the General Electric Company on Behalf of its Division, GE Healthcare Signature: Printed Name: Title: Date: Before using this document, make sure it is the latest revision. Access My Workshop to verify the current revision. If you do not have access to, or are unfamiliar with, the My Workshop system, consult your quality representative. DOC0288647 Dear GE Healthcare BIS Sensor Customer For 10 years GE Healthcare and Aspect Medical Systems have worked together to provide anesthesia and critical care providers BIS technology through GE BIS modules, and Aspect BIS Sensors. Effective April 1st, 2009, Aspect will take over worldwide distribution of BIS sensors. GE and Aspect are making every effort to provide a seamless transition of your BIS sensor needs. If you have a BIS Sensor contract with GE, both companies will work together to ensure that contractual obligations continue to be met through the contract’s term. GE will supply BIS sensors to customers with long-term sensor commitments until such contracts. GE Healthcare will continue marketing and supporting BIS modules as they have done since their integration into GE monitors. Educational, technical and customer support for BIS sensors will be provided by Aspect Medical, or its authorized representative, while GE Healthcare will continue to provide direct support for all GE branded equipment, including the BIS module/BISx. Both GE and Aspect are committed to continue to serve you in the best way. For further questions kindly contact your GE or Aspect representative. For your reference, a list of local Aspect representatives can be found at the following website: xxxx:...
Sample 1
Quality and Safety Reporting. The Supplier shall maintain a documented reporting system to GE Healthcare when the Supplier has knowledge of any product issue related to safety or quality that results in stopping shipment or requires a recall. Any actions taken by the Supplier to report a recall to a regulated agency must be communicated to GE Healthcare immediately (within 24 hours). GE Healthcare has the right to request Supplier to provide all documents regarding the specific issue including the analysis, root cause and corrective action taken to minimize any risk to GE Healthcare customers. Before using this document, assure it is the latest revision. 7.4.2-01F-GQP See eLibrary DOC0079550 for current revision. Revision: 01 Due for Review: 10/2007 GE Healthcare Minimum Purchased Material Quality Requirements
Sample 1
Quality and Safety Reporting. Supplier will maintain a documented reporting system for notifying INVACARE when Supplier has knowledge of any product issue related to safety or quality that requires an immediate stop-shipment or recall of Supplier’s product that has or will be delivered to INVACARE. Such report shall be submitted 1 business day after discovery.
Sample 1
Quality and Safety Reporting a. The Practice will notify Badger within five working days of becoming aware of any breach of legislation or any adverse determination of the CQC or any other regulatory body or statutory agency.
Sample 1

Related to Quality and Safety Reporting

  • Environmental, Health and Safety Matters (a) The Company has complied and is in compliance with all Environmental, Health, and Safety Requirements.

  • Environmental, Health and Safety i. Environment, Health and Safety Performance. Seller acknowledges and accepts full and sole responsibility to maintain an environment, health and safety management system ("EMS") appropriate for its business throughout the performance of this Contract. Buyer expects that Seller’s EMS shall promote health and safety, environmental stewardship, and pollution prevention by appropriate source reduction strategies. Seller shall convey the requirement of this clause to its suppliers. Seller shall not deliver goods that contain asbestos mineral fibers.

  • Health and Safety C8.1 The Contractor shall promptly notify the Authority of any health and safety hazards which may arise in connection with the performance of the Contract. The Authority shall promptly notify the Contractor of any health and safety hazards which may exist or arise at the Authority’s Premises and which may affect the Contractor in the performance of the Contract.

  • Environmental, Health and Safety Laws There does not exist any violation by the Borrower or any Subsidiary of any applicable federal, state or local law, rule or regulation or order of any government, governmental department, board, agency or other instrumentality relating to environmental, pollution, health or safety matters which will or threatens to impose a material liability on the Borrower or a Subsidiary or which would require a material expenditure by the Borrower or such Subsidiary to cure. Neither the Borrower nor any Subsidiary has received any notice to the effect that any part of its operations or properties is not in material compliance with any such law, rule, regulation or order or notice that it or its property is the subject of any governmental investigation evaluating whether any remedial action is needed to respond to any release of any toxic or hazardous waste or substance into the environment, the consequences of which non-compliance or remedial action could constitute an Adverse Event.

  • Environment, Health, and Safety 24.4.1. The Supplier and its staff (and/or any sub-supplier and/or subcontractor) shall comply with the laws and regulations in force related to protection of the environment, the health and safety instructions applicable to the Goods and Services performed pursuant to the Contract and especially, if appropriate, to the Goodsand Services performedon any Site by a third company.

  • Quality Standards Each Party agrees that the nature and quality of its products and services supplied in connection with the other Party's Marks will conform to quality standards set by the other Party. Each Party agrees to supply the other Party, upon request, with a reasonable number of samples of any Materials publicly disseminated by such Party which utilize the other Party's Marks. Each Party will comply with all applicable laws, regulations, and customs and obtain any required government approvals pertaining to use of the other Party's marks.

  • Quality Requirements Performance Indicator Heading Indicator (specific) Threshold Method of Measurement Frequency of monitoring Consequence of Breach QUALITY Patient Safety - Incidents I1 Number of incidents Adverse incidents include the following: clinical or non clinical adverse events that have potential to cause avoidable harm to a patient, including medical errors or adverse events related to medical devices or other equipment. Clinical or non- clinical accidents, accidental injuries to staff and members of the public, verbal, physical or psychological abuse or harassment, unusual or dangerous occurrences, damage to trust property, plant or equipment, fire or flood, security, theft or loss, near misses are identified as any event where under different circumstances significant injury or loss may have occurred Number of recorded incidents in the contract month Monthly Remedial Action Plan brought to Performance Meeting following breach; action under Module C Clause 32 if needed I2 Number of Sis Definition of SUI according to trust policy and national guidance Number of Serious Untoward Incidents reported in contract month Monthly Remedial Action Plan brought to Performance Meeting following breach; action under Module C Clause 32 if needed S1 Percentage of eligible staff received child safeguarding training at level 2 (as identified in LSCB training strategy) 95% Number received training/ Number of identified staff requiring training Monthly S2 Percentage of eligible staff received adult safeguarding awareness training at level 2 ( as identified in K&M Safeguarding Vulnerable Adults training strategy) 95% Number of staff trained/ Number of identified staff requiring training Monthly

  • Environmental and Safety Matters Except as disclosed in Schedule 4.13:

  • Quality Specifications SANMINA-SCI shall comply with the quality specifications set forth in its Quality Manual, incorporated by reference herein, a copy of which is available from SANMINA-SCI upon request.

  • Adverse Event Reporting Both Parties acknowledge the obligation to comply with the Protocol and / or applicable regulations governing the collection and reporting of adverse events of which they may become aware during the course of the Clinical Trial. Both Parties agree to fulfil and ensure that their Agents fulfil regulatory requirements with respect to the reporting of adverse events.

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