Other Regulatory Matters. Each Party will promptly provide the other Party with copies of all material documents, information and correspondence received from a Regulatory Authority (including a written summary of any material communications in which such other Party did not participate) within the Territory and, upon reasonable request, with copies of any other documents, reports and communications from or to any Regulatory Authority within the Territory relating to the Compound, the Product and/or activities under this Agreement.
Appears in 3 contracts
Samples: Certain (Xenoport Inc), Certain (Xenoport Inc), Development and Commercialization Agreement (Xenoport Inc)
Other Regulatory Matters. Each Party will promptly provide the other Party with copies of all material documents, information and correspondence received from a Regulatory Authority (including a written summary of any material communications in which such other Party did not participate) within the Territory and, upon reasonable request, with copies of any other documents, reports and communications from or to any Regulatory Authority within the Territory relating to the CompoundVGX-3100, the Product Delivery Device and/or Products or activities under this the Agreement.
Appears in 2 contracts
Samples: License and Collaboration Agreement, License and Collaboration Agreement (Inovio Pharmaceuticals, Inc.)
Other Regulatory Matters. Each Party will promptly provide the other Party with copies of all material documents, information and correspondence received from a Regulatory Authority (including a written summary of any material communications in which such other Party did not participate) pertaining to Products within the Territory and, upon reasonable request, with copies of any other documents, reports and communications from or to any Regulatory Authority within the Territory relating to the Compound, the a Product and/or or activities under this Agreement.
Appears in 2 contracts
Samples: Development and Commercialization Agreement (La Jolla Pharmaceutical Co), Development and Commercialization Agreement (Biomarin Pharmaceutical Inc)
Other Regulatory Matters. Each Subject to Sections 5.3(a) and 5.7(b), each Party will promptly provide the other Party with copies of all material documents, information and correspondence received from a Regulatory Authority within the Territory relating to Product or activities under this Agreement (including a written summary of any material communications in which such other Party did not participate) within the Territory and, upon reasonable request, with copies of any other documents, reports and communications from or to any Regulatory Authority within the Territory relating to the Compound, the Product and/or or activities under this the Agreement.
Appears in 1 contract
Samples: License Agreement (Tocagen Inc)
Other Regulatory Matters. Each Party will promptly provide the other Party with copies of all material documents, information and correspondence received from a any Regulatory Authority (including a written summary of any material communications in which such other Party did not participate) within the Territory and, upon reasonable request, with copies of any other documents, reports and communications from or to any Regulatory Authority within the Territory relating to Product for the Compound, Field in the Product and/or activities under this AgreementTerritory.
Appears in 1 contract
Samples: Development and Commercialization Agreement (Mesoblast LTD)