Task 6: CGMP Drug Substance Run and Stability Testing Task 5: Engineering Drug Substance Run and Stability Testing Task 4: Process Scale-Up and Optimization Task 3: CGMP Master Cell and Working Cell Banks Task 1: Technology Transfer and Process Establishment This proposal consists of eight tasks required for to complete the project, including: Ology Bio’s experienced team of Subject Matter Experts and qualified subcontractors will comply with all applicable regulatory requirements to accomplish the scope of work. To achieve the client’s goal of process development and CGMP manufacturing of the live attenuated Streptococcus pneumoniae vaccine program, Blue Water requires the services of a CDMO. NOW, THEREFORE, in consideration of the foregoing and the mutual promises, covenants and agreements set forth below, and for other good and valuable consideration, the receipt and sufficiency of which the parties hereby acknowledge, the parties agree as follows: WHEREAS, Blue Water and Ology Bio desire to enter into this Project Addendum II for Services as set forth herein, subject to and in accordance with the MSA. WHEREAS, Blue Water and Ology Bio entered into a Master Services Agreement effectively dated as of July 19, 2019, (the “MSA”) whereby Ology Bio agreed to provide from time to time services and deliverables associated therewith (“Services”) to Client pursuant to the terms and conditions set forth in the MSA and any Project Addendum Blue Water and Ology Bio are sometimes referred to herein individually as a “Party” and collectively as the “Parties.” This Project Addendum is effectively dated as of (the “Effective Date”) by and between Blue Water Vaccines, Inc., a Delaware corporation having a principal place of business at 15 East Putnam Avenue, Suite 363, Greenwich, CT 06830 (“Blue Water” or “Client”), and Ology Bioservices, Inc., a Delaware corporation having a principal place of business at 13200 NW Nano Court, Alachua, Florida 32615 (“Ology Bio”). PROJECT ADDENDUM II TO MASTER SERVICES AGREEMENT
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