Study Medication definition

Study Medication means the study drug or control material as defined in the Protocol. “CRO” shall mean a clinical research organisation holding an agreement with the Sponsor for services in regards to the Study conduct. The CRO is a signatory to this Agreement, on behalf of the Sponsor, in order to facilitate the contracting process for the Sponsor. However, the CRO does not take over any Sponsor’s obligations related to this Agreement. The Sponsor is represented by the CRO that acts with the Power of Attorney from the Sponsor (attached as Appendix B). „Hodnocený lék“ je hodnocené léčivo nebo kontrolní materiál definované v Protokolu. „CRO“ je klinická výzkumná organizace, která uzavřela smlouvu se Zadavatelem týkající se služeb při provádění Studie. CRO je podepisující stranou této Smlouvy jménem Zadavatele s cílem podpořit smluvní proces pro Zadavatele. CRO však nepřebírá žádné závazky Zadavatele vyplývající z této Smlouvy. Zadavatel je zastoupen CRO, která působí na základě plné moci od Zadavatele (připojena jako Příloha B).
Sample 1
Study Medication means SEARXX'x xxxpound SC-58635. 3 - 3 -
Sample 1
Study Medication administration Day 4: During this visit the following will be done: • Review of your medications and review of any symptoms or side effects that you may be experiencing or have experienced since the last visit • Routine blood and urine sample collections to check your overall health Day 8: During this visit the following will be done: • Review of your medications and review of any symptoms or side effects that you may be experiencing or have experienced since the last visit • Routine blood and urine sample collections to check your overall health • PK blood sample collection – one sample Subsequent Cycles If you tolerated the first cycle and remain on the study, you will continue to receive the study medication on Day 1 of each 21-day (3 week) cycle. During each cycle, you will also need to have the following tests and procedures. Day 1: During this visit premedication will be administered and the following will be done: • Review of your medications and review of any symptoms or side effects that you may be experiencing or have experienced since the last visit • Xxxxx xxxxx • Physical exam including body weight and lung assessment, and assessment of your performance status • Routine blood and urine sample collections to check your overall health • PK blood sample collection – one sample before getting your study medication; one sample at the end of infusion during Cycle 5 only • ADA blood sample collection • Premedication administration
Sample 1

Examples of Study Medication in a sentence

  • All Study Medication shall be used by the Site, under the supervision of the Investigator, solely for the purpose of conducting the Study according to the Protocol.

  • The Investigator shall not supply the Study Medication to any person not authorized under Applicable Law to receive it.

  • Percent of Subjects Experiencing Grade 3+ Adverse Events (or Grade 3+ Adverse Events Attributed to the Study Medication) with Exact 95% Confidence Intervals Table 7 presents exact 95% confidence intervals around various potential rates of Grade 3+ adverse events which might be observed in a total sample of 36 evaluable subjects, a sample of 12 subjects representing a minimal sample that might be accrued within any age stratum and potential sample size that might occur if a subgroup of N = 24 was analyzed.

  • This research has tried to select films ranging in genre from drama/soap opera, action/adventure/martial arts to the magical/mythical.

  • The Study Medication shall be stored at such temperature and other conditions as reasonably required by Sponsor and as required by the Protocol.

  • Relationship of Study Medication to Adverse Events UnrelatedThe study drug almost certainly (or certainly) did not cause the event.

  • Sponsor agrees to indemnify, defend and hold harmless Institution, its trustees, officers, employees, staff, subcontractors, and agents (“Institution Indemnitees”) against any independent third party claim (each, a “Claim”) arising out of (i) any theory of product liability concerning the Study Medication or (ii) any side-effect or adverse reaction, illness, or injury directly resulting from use of the Study Medication in the Study.

  • Table 2 Study Medication Information Study Medication Name*Excursions from these temperature ranges must be reported to Aclaris.

  • We are proposing to adopt Option 1 for establishing ACO benchmarks, but seek comments on the merits and limitations of both options, particularly with respect to how each approach might affect the willingness of ACOs or particular types of ACO to participate in the Shared Savings Program, create incentives for ACOs to seek or avoid certain kinds of beneficiaries, and impact Medicare expenditures.

  • If the actual closing date is later, it is possible to inadvertently miss the 45-day deadline, rendering the proposed exchange fully taxable.


More Definitions of Study Medication

Study Medication administration Day 8: During this visit the following will be done: • Review of your medications and review of any symptoms or side effects that you may be experiencing or have experienced since the last visit • Routine blood and urine sample collections to check your overall health • PK blood sample collection – one sample during Cycle 5 only End of Even-Numbered Cycles (Cycle 2, 4, 6, etc.) During the week prior to Day 1 of the next cycle: During this visit, the following will be done: • Review of your medications and review of any symptoms or side effects that you may be experiencing or have experienced since the last visit • CT scan or MRI to assess your disease and check your lung status • End of Cycle 2 only: Ophthalmology Exam
Sample 1
Study Medication means the pharmaceutical compound that is the subject of the Study.
Sample 1

Related to Study Medication

  • Medication means any drug, chemical, compound, suspension, or preparation in suitable form for use as a curative or remedial substance taken either internally or externally by any person.

  • Nonprescription medication means a drug or medication authorized pursuant to federal or state law for general distribution and use without a prescription in the treatment of human disease, ailments, or injuries.

  • Prescription medication means any medication that requires a physician prescription before it may be obtained from a pharmacist.

  • Study means the investigation to be conducted in accordance with the Protocol.

  • Prosthesis means an artificial substitute for a missing body part.

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

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Antipsychotic medications means that class of drugs

  • Psychotropic medication means medication the prescribed intent of which is to affect or alter thought processes, mood, or behavior including but not limited to anti-psychotic, antidepressant, anxiolytic (anti-anxiety), and behavior medications. The classification of a medication depends upon its stated, intended effect when prescribed.

  • Tissue means a portion of the human body other than an organ or an eye. The term does not include blood unless the blood is donated for the purpose of research or education.

  • Medical cannabis means the same as that term is defined in Section 26-61a-102.

  • Veterinarian means a veterinarian authorized by law to practice veterinary medicine in this State.

  • Screening means the evaluation process used to identify an individual's ability to perform activities of daily living and address health and safety concerns.

  • Study Site means the location(s) under the control of the Institution where the Study is actually conducted as set out in Schedule 1.

  • Medical cannabis card means the same as that term is defined in Section 26-61a-102.

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Cannabis means all parts of the plant Cannabis sativa Linnaeus, Cannabis indica, or Cannabis ruderalis, whether growing or not; the seeds thereof; the resin, whether crude or purified, extracted from any part of the plant; and every compound, manufacture, salt, derivative, mixture, or preparation of the plant, its seeds, or resin. “Cannabis” also means the separated resin, whether crude or purified, obtained from cannabis. “Cannabis” does not include the mature stalks of the plant, fiber produced from the stalks, oil or cake made from the seeds of the plant, any other compound, manufacture, salt, derivative, mixture, or preparation of the mature stalks (except the resin extracted therefrom), fiber, oil, or cake, or the sterilized seed of the plant which is incapable of germination. For the purpose of this division, “cannabis” does not mean “industrial hemp” as defined by Section 11018.5 of the Health and Safety Code. Cannabis and the term “marijuana” may be used interchangeably.

  • Medical Specialist means any medical practitioner who is vocationally registered by the Medical Council under the Health Practitioners Competence Assurance Act 2003 in one of the approved branches of medicine and who is employed in either that branch of medicine or in a similar capacity with minimal oversight.

  • Manufacturing Process means any process for—

  • Sterilization means the procedure that kills all microorganisms, including their spores.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Vaccine means a specially prepared antigen which, upon administration to a person, will result in immunity and, specifically for the purposes of this rule, shall mean influenza and pneumococcal vaccines.

  • Licensed mental health professional or "LMHP" means a physician, licensed clinical psychologist, licensed professional counselor, licensed clinical social worker, licensed substance abuse treatment practitioner, licensed marriage and family therapist, certified psychiatric clinical nurse specialist, licensed behavior analyst, or licensed psychiatric/mental health nurse practitioner.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Orthotics means the science and practice of evaluating, measuring, designing, fabricating, assembling, fitting, adjusting, or servicing an orthosis under an order from a licensed physician or podiatrist for the correction or alleviation of neuromuscular or musculoskeletal dysfunction, disease, injury, or deformity.

  • 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.