Product Sponsor definition

Product Sponsor as used herein refers to the distributor or issuer of any financial services or products sold through MOIS and may include: • a mutual fund, exchange traded fund (“ETF”) or other Company registered under the Investment Company Act of 1940; • an insurance company that issues variable annuity and/or variable life products; or offers access to a retirement plan platform; or • a company registered with the Securities and Exchange Commission (“SEC”) whose securities are registered and available for purchase or sale in your accounts through your broker-dealer. • “Qualified Custodian” refers to the bank, clearing firm or trust company holding your securities and/or funds. • “Third-Party Money Manager” refers to the third-party investment advisers that MOIS and Advisor may refer You to under the Third-Party Money Manager service.
Sample 1Sample 2
Product Sponsor as used herein refers to the distributor or issuer of any financial services or products sold through MOIS and may include: • a mutual fund, exchange traded fund (“ETF”) or other Company registered under the Investment Company Act of 1940; • an insurance company that issues variable annuity and/or variable life products; or • a company registered with the Securities and Exchange Commission (“SEC”) whose securities are registered and available for purchase or sale in your accounts through your broker-dealer. • “Qualified Custodian” refers to the bank, clearing firm or trust company holding your securities and/or funds. • “Third-Party Money Manager” refers to the third-party investment advisers that MOIS and Advisor may refer You to under the Third-Party Money Manager service.
Sample 1
Product Sponsor as used herein refers to the distributor or issuer of any financial services or products sold through MOIS and may include: • a mutual fund, exchange traded fund (“ETF”) or other Company registered under the Investment Company Act of 1940; • an insurance company that issues group variable annuity products; • an insurance company that issues variable annuity and/or variable life products or offers access to a retirement plan platform; or • a company registered with the Securities and Exchange Commission (“SEC”) whose securities are registered and available for purchase or sale in your accounts through your broker-dealer. • “Qualified Custodian” refers to the bank, clearing firm or trust company holding your securities and/or funds. • “Third-Party Money Manager” refers to the third-party investment advisers that MOIS and Advisor may refer You to under the Third-Party Money Manager service.
Sample 1

Examples of Product Sponsor in a sentence

  • LPL acts as the broker to the Plan account established at the Product Sponsor or Platform Provider (“Service Provider”) identified in the Account Application.

  • If the parties do not reach agreement within 15 days of starting negotiations, the biosimilar applicant must notify the Reference Product Sponsor of the number of patents it will provide in a second list, and the parties then simultaneously exchange within five days of this notice a list of patents that each party believes should be the subject of infringement litigation.

  • The Reference Product Sponsor must also identify which, if any, of these patents it would be prepared to license to the biosimilar applicant.

  • If the parties reach agreement within 15 days of starting negotiations, the Reference Product Sponsor must bring a patent-infringement action against the biosimilar applicant on the negotiated list of patents within 30 days of such agreement.

  • Even after the litigation contemplated by 42 U.S.C. § 262( l)(6)(B) has commenced, the Reference Product Sponsor must identify additional patents that are newly issued or licensed after the Reference Product Sponsor provided its patent list under 42 U.S.C. § 262(l)(3)(A).

  • Specifically, the Reference Product Sponsor must, not later than 30 days after the issuance or licensing, supplement that list with the newly issued or licensed patent(s).

  • In the absence of such a disclosure, the Reference Product Sponsor has no access to the manufacturing information.

  • Such charges may vary depending on the product type, size, method of investment (online, telephone, via representative), Product Sponsor and Representative.

  • CH2 – Phenylephrine 0.5mg/5mL (Item Ref No 4102): Product Sponsor change, Interpharma to Advanz Pharma effective 01/03/2021.

  • You understand that the failure to do could result in an unauthorized person gaining access to your accounts or information maintained by you, the Qualified Custodian or a Product Sponsor.

Related to Product Sponsor

  • Participating manufacturer means that term as defined in the master settlement agreement.

  • Participating Hospice Care Program Provider means a Hospice Care Program Provider that either: (i) has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield to provide services to participants in this benefits program, or; (ii) a Hospice Care Program Provider which has been designated by a Blue Cross and/or Blue Shield Plan as a Participating Provider Option program.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Non-Participating Hospice Care Program Provider means a Hospice Care Program Provider that either: (i) does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield to provide services to participants in this benefits program, or; (ii) a Hospice Care Program Provider which has not been designated by a Blue Cross and/or Blue Shield Plan as a Participating Provider Option program.

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

  • Participating Product means any of the Breville products listed in the table below by model name and number that are supplied by Breville in Australia and sold directly by Breville or by a Participating Retail Store: Any costs, fees, expenses or liability of any description to pay any amount for installation, insurance, warranty or extended warranty, delivery or any other cost that is, at the determination of the Promoter in its absolute discretion, additional or ancillary to the models listed in the above table.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Wholesale drug distributor means anyone engaged in the

  • Marketing program means a program established by order of the director pursuant to this act prescribing rules and regulations governing the marketing for processing, distributing, selling, or handling an agricultural commodity produced in this state or agricultural commodity input during a specified period and

  • Distillery manufacturing license means a license issued in accordance with

  • Commercialization Plan has the meaning set forth in Section 6.2.

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • Non-Participating Clinical Laboratory means a Clinical Laboratory which does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan provide services to you at the time services are rendered.

  • Clinical practice guidelines means a systematically developed statement to assist

  • Non-Participating Clinical Professional Counselor means a Clinical Professional Counselor who does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Covered Products means Your Applications, Libraries, Passes, Safari Extensions, Safari Push Notifications, and/or FPS implementations developed under this Agreement.

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Manufactured products means items and construction materials composed in whole or in part of non-ferrous metals such as aluminum; plastics and polymer-based products such as polyvinyl chloride pipe; aggregates such as concrete; glass, including optical fiber; and lumber.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Participating Clinical Professional Counselor means a Clinical Professional Counselor who has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Third Party Manufacturer means (i) a Third Party whose primary business is contract manufacturing, or (ii) a Third Party who has a contractual arrangement with Licensee or with a sublicensee of Licensee that includes manufacturing of Client Product and/or Drug Product by such Third Party for Licensee or such sublicensee.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.