LTS’ Support of Registration. LTS shall provide to NuPathe in a timely manner the information which concerns the design and manufacture of the Product necessary for preparing the applicable regulatory documents for NuPathe’s regulatory filings and shall use its Commercially Reasonable Efforts to provide NuPathe support reasonably required for such filing for one Major Market Country. Subject to regulatory requirements, in the event that this requires disclosure of LTS Know-How or confidential information of LTS customers, LTS shall have the right to communicate such information directly to the health authorities, without disclosing same to NuPathe. All INDs, NDAs and other regulatory filings made or filed by NuPathe with respect to any Products shall be in the name of, and be owned solely by NuPathe. In the event NuPathe wishes additional support from LTS for the registration in other countries, any activities shall be subject to the terms and conditions of this agreement, provided, however, that such support from LTS shall be subject to a written agreement including LTS’ compensation and the timelines for such support.
Appears in 2 contracts
Sources: Development and License Agreement (Nupathe Inc.), Development and License Agreement (Nupathe Inc.)