Oregon Sales, Distribution and Development Agreement between Supergen, Inc. and Abbott Laboratories regarding clinical development, obtaining of regulatory approvals

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US-EG-9278
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Worldwide Sales, Distribution and Development Agreement between Supergen, Inc. and Abbott Laboratories regarding the clinical development, obtaining of regulatory approvals, distribution and marketing of Rubitecan products throughout the world dated

The Oregon Sales, Distribution, and Development Agreement between Supermen, Inc. and Abbott Laboratories is a comprehensive contractual agreement that outlines the partnership between the two companies in the realm of clinical development and regulatory approval. This agreement enables Supermen, Inc. to distribute and sell Abbott Laboratories' products in the state of Oregon, while also providing a framework for jointly developing new products and obtaining necessary regulatory approvals. Key elements of the agreement include: 1. Scope of Collaboration: The agreement defines the specific products and services that will be involved in the collaboration, whether they are existing offerings or potential new developments. It outlines the geographic scope of the agreement, focusing on the state of Oregon as the target market. 2. Sales and Distribution: The agreement establishes the rights and responsibilities of both companies concerning the sale and distribution of Abbott Laboratories' products within Oregon. It may outline aspects such as market exclusivity, pricing, marketing support, and any incentives or commissions for Supermen, Inc. based on sales performance. 3. Clinical Development: This agreement may encompass provisions for joint clinical development activities, where Supermen, Inc. and Abbott Laboratories collaborate on the research, development, and testing of new healthcare products. It may define the roles and contributions of both parties, including funding responsibilities, data sharing, and intellectual property ownership. 4. Regulatory Approvals: Given the importance of obtaining regulatory approvals for the sale and distribution of healthcare products, this agreement will outline the cooperative efforts of Supermen, Inc. and Abbott Laboratories to secure necessary licenses, permits, and clearances. It may establish the procedures for submitting applications, conducting clinical trials, and addressing regulatory obligations to comply with state and federal laws. 5. Intellectual Property Rights: The agreement will address the ownership and protection of intellectual property resulting from collaborative activities. It may define how intellectual property rights are shared or assigned between the parties, ensuring fair compensation and safeguards against unauthorized use or disclosure. 6. Performance Metrics and Dispute Resolution: To ensure accountability and maintain a productive partnership, this agreement could specify performance metrics and milestones that Supermen, Inc. must achieve in terms of sales targets and development timelines. Additionally, it may lay out dispute resolution mechanisms, such as mediation or arbitration, to resolve conflicts that may arise during the collaboration. If there are different types of Oregon Sales, Distribution, and Development Agreements between Supermen, Inc. and Abbott Laboratories specifically tailored for clinical development and obtaining regulatory approvals, they may be classified based on specific therapeutic areas, product categories, or targeted patient populations. These variations in agreements aim to address the unique requirements and regulations associated with different healthcare sectors, enabling a more focused and effective collaboration.

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Download Sales, Distribution and Development Agreement between Supergen, Inc. and Abbott Laboratories regarding clinical development, obtaining of regulatory ... Obtaining and providing Abbott with copies of Regulatory Filings as necessary for Abbott to obtain regulatory approval of the pre-approval inspection; and. d ...Oregon Laboratories - get access to a huge library of legal forms. Professionally drafted and regularly updated online templates. Easily download and print ... The costs of both GCP Audits shall be borne by AVI and SuperGen. If SuperGen is the Party responsible for the clinical development and regulatory approval of ... ABBOTT LABORATORIES HEREBY DISCLAIMS ALL REPRESENTATIONS AND WARRANTIES, WHETHER EXPRESS OR IMPLIED, CREATED BY LAW, CONTRACT OR OTHERWISE, INCLUDING, WITHOUT ... View Abbott Laboratories contracts and agreements from SEC filings. Including company executives, business partners, clauses and more. QuickLinks - Click here to rapidly navigate through this document Exhibit (a)(1)(E) Offer to Purchase for Cash All Outstanding Shares of Common Stock of ASTEX ... Feb 22, 2019 — ... regulatory approval based on data obtained in controlled clinical trials of limited duration. ... clinical trials) for obtaining regulatory ... All job applicants are required to successfully complete a drug screen before employment with Abbott. Applicants refusing to consent to pre-employment screening ... Principal companyPartner companyValue ($M)4SC AG (Germany)Serono SA (Switzerland; NYSE:SRA)$67.004SC AG (Germany)Mutabilis SA (France)7TM Pharma A/S (Denmark)AstraZeneca plc (UK)

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Oregon Sales, Distribution and Development Agreement between Supergen, Inc. and Abbott Laboratories regarding clinical development, obtaining of regulatory approvals