Labeling and Marketing Materials. Endo shall have sole authority and responsibility to seek and/or obtain any necessary Governmental or Regulatory Authority approvals of any labeling, package inserts, Product monographs, packaging for the Products and Marketing Materials, and for determining whether the same requires Governmental or Regulatory Authority approval. As between the parties, all filings and communications with Governmental or Regulatory Authorities in connection therewith shall remain under the control of Endo.
Labeling and Marketing Materials. To the extent transferable (but excluding materials not reasonably separable from materials that do not relate primarily or exclusively to the Business), all Product labeling materials and all Product advertising, marketing, environmental, medical communication and promotional materials (including congress and symposium materials, marketing plans, sales training materials and other marketing-related information and materials) as well as all Websites, in each case, to the extent primarily or exclusively relating to the Business or owned or purported to be owned by any Acquired Company (the “Transferred Labeling and Marketing Materials”).
Labeling and Marketing Materials. Santarus shall have sole authority and responsibility to seek and/or obtain any necessary Governmental or Regulatory Authority approvals of any labeling, package inserts, packaging for the Products and Marketing Materials, and for determining whether the same requires Governmental or Regulatory Authority approval. As between the parties, all filings and communications with Governmental or Regulatory Authorities in connection therewith shall remain under the control of Santarus. No Product labeling, package inserts, packaging for the Products or Marketing Materials may be used or distributed by Co-Promotion Partner unless such labeling, package inserts, packaging for the Products or Marketing Materials have been approved in advance by Santarus. Santarus shall provide Co-Promotion Partner with (i) prompt notice of, and copies of, any changes in the Product(s) label or labeling; and (ii) upon written request by Co-Promotion Partner, periodic updates on the progress of regulatory review by FDA for all Product(s) not yet approved for marketing by FDA.
Labeling and Marketing Materials. If Vendor is labeling the merchandise with the private label(s) of Amcraft vendor shall bear the cost of printing said labels, which shall not be modified, removed or replaced without the express written consent of ABC. Vendor shall provide reasonable quantities of Vendor’s most current literature, including any material safety data sheets, and any updates as needed, to Amcraft for its use to ensure that Amcraft and ABC remain adequately informed as to the intended uses, qualities, specifications and limitations of use regarding the merchandise. Vendor acknowledges that Amcraft is the owner of all marks, trade dress and related material provided to Vendor by ABC for such private labeling.
Labeling and Marketing Materials. No Co-Promotion Collaboration Product labeling, package inserts, monographs, packaging for the Co-Promotion Collaboration Product or Marketing Materials may be used or distributed by the parties unless such labeling, package inserts, monographs, packaging for the Co-Promotion Collaboration Products or Marketing Materials have been approved in advance in accordance with Section 6.2(a) hereof.
Labeling and Marketing Materials. Galderma shall be solely responsible for obtaining any necessary governmental or regulatory authority approvals of any labeling, package inserts, Product monographs, packaging for the Products and Marketing Materials, and for determining whether the same requires governmental or regulatory authority approval. No Product labeling, package inserts, Product monographs, packaging for the Products or Marketing Materials may be used or distributed by PhotoMedex unless such labeling, package inserts, Product monographs, packaging for the Products or Marketing Materials have been approved in advance by Galderma.
Labeling and Marketing Materials. The Clinical/Regulatory Sub-Committee shall coordinate strategy and policy for obtaining any necessary Governmental or Regulatory Authority approvals of any labeling, package inserts, Product monographs, packaging for the Products and Marketing Materials, and for determining whether the same requires Governmental or Regulatory Authority approval, subject to Ligand's review and approval. As between the parties, all filings and communications with Governmental or Regulatory Authorities in connection therewith shall be the obligation and responsibility solely of Ligand. No Product labeling, package inserts, Product monographs, packaging for the Products or Marketing Materials may be used or distributed by Co-Promotion Partner unless such labeling, package inserts, Product monographs, packaging for the Products or Marketing Materials have been approved in advance by Ligand.
