Xxxxxx Laboratory definition

Xxxxxx Laboratory means all individuals within the Xxxxxx Laboratory at Penn that report directly to, or are under the direct supervision or control of, Xxxxx X. Xxxxxx, MD, PhD.
Sample 1Sample 2Sample 3
Xxxxxx Laboratory means Xx. Xxxxx X. Wilson and all individuals [*].
Sample 1Sample 2Sample 3

Examples of Xxxxxx Laboratory in a sentence

  • Penn, through Dr. Xxxxx Xxxxxx and the Xxxxxx Laboratory, have technology and expertise in the research and development of Gene Therapy Products, including with respect to Gene Therapy Products for the treatment of genetic disorders associated with the liver.

  • Absent Licensee’s prior written consent to the contrary, the Xxxxxx Laboratory will solely perform the work under the Research Program on behalf of Penn.

  • Wilson and the Xxxxxx Laboratory, have technology and expertise in the research and development of gene therapy products.

  • During the Research Term, Penn Orphan Center, through the Xxxxxx Laboratory, shall conduct natural history studies relating to the Research Program with funding from the Licensee and additional commercial Third Parties, subject to the Parties’ having reached mutual agreement upon the terms of the funding, non-exclusive rights to the data arising from such studies and other terms in a clinical research agreement.

  • During the Research Term, if Licensee wishes to include a new Gene Therapy Product development program for a CNS Monogenic Rare Disorder to be conducted in the Xxxxxx Laboratory for a New Indication, then Licensee may formally make such request in writing to Penn during the Research Term.

  • This Lease (this "Lease") is entered into as of April ___, 1994, by and between The Xxxxxxx Xxxxx Xxxxxx Laboratory, Inc.

  • If Licensee agrees to the proposed substitution, the Parties will amend the definition of the Xxxxxx Laboratory (effective on a going-forward basis) to describe the group within Penn that will be continuing the Research Program and Next Generation Program.

  • For each available Next Generation Capsid developed before the AAV Option Period, the Xxxxxx Laboratory will provide a Next Generation Capsid Data Package if reasonably requested by Licensee.

  • Xxxx Title: President & COO Agen Biomedical Limited Signature: /s/ XXXXXX HOME Name: Xxxxxx Home Title: Managing Director Cryonix Signature: /s/ XXXXXX XXXXX Name: Xxxxxx Xxxxx Title: Head of Repository Operations Date: 3.Nov.2004 Xxxxxx Laboratory Products PLC Signature: /s/ X.

  • During the term of the Next Generation Program, Penn, through the Xxxxxx Laboratory, will notify Licensee of any available Next Generation Capsids (in accordance with the applicable provisions of Section 2.9.4).

Related to Xxxxxx Laboratory

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Testing laboratory means a laboratory, facility, or entity in the state that offers or performs tests of cannabis or cannabis products and that is both of the following:

  • Laboratory or “LANL” means the geographical location of Los Alamos National Laboratory, a federally funded research and development center owned by the DOE / NNSA.

  • Good Laboratory Practice or “GLP” means the applicable then-current standards for laboratory activities for pharmaceuticals (including biologicals) or vaccines, as applicable, as set forth in the Act and any regulations or guidance documents promulgated thereunder, as amended from time to time, together with any similar standards of good laboratory practice as are required by any Regulatory Authority having jurisdiction over the applicable activity.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Quality system means documented organizational procedures and policies: internal audits of those policies and procedures: management review and recommendation for quality improvement.”

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • API means American Petroleum Institute.

  • scientific research means any activity in the field of natural or applied science for the extension of knowledge;

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.

  • Manufacturing Know-How means, with respect to the Product or any Variant thereof, the technology, data, designs, processes, methods, specifications and other know-how used in connection with the formulation, manufacture, labeling, packaging, quality control, release testing, and production of the Product, and all ingredients used therein and portions thereof.

  • Good Laboratory Practices or “GLP” means the then-current good laboratory practice standards promulgated or endorsed by the FDA, as defined in U.S. 21 C.F.R. Part 58 (or such other comparable regulatory standards in jurisdictions outside the United States, as they may be updated from time to time).