Were all seven steps of the scientific method referenced in the Drug X report summary in this exercise? Explain your answer by correlating each step to information provided in the report summary. Step 1 is Make an Observation, Step 2 is Ask a question & research, Step 3 is formulate a hypothesis, step 4 is test hypothesis, step 5 is analyze data and draw conclusions, step 6 is peer review verification, step 7 is communicate results Was the reported study data in this exercise qualitative or quantitative? Explain your answer by referencing the definitions of each data

Match each term regarding responsible conduct of research with the best definition/ explanation: A. violation of ethical standards outside of fabrication, falsification, or plagiarism B. fabrication, falsification, or plagiarism in reporting research results C. application of honesty, fairness, objectivity, openness, trustworthiness, and respect to scientific endeavors. D. conduct that can vary between disciplines and laboratories 1. scientific standard select A B C D 2. scientific misconduct select A B C D 3. questionable research practices select A B C D 4. scientific practices

AHS 131 - Skeletal System - Bone Composition, Structures, Bone Names and their parts. These are the structures and names that you will need to know for your AHS 131 Bone Lab Exam. Please review and rewrite the names in the space below. When appropriate include the function of the structure. Axial Skeleton Skull Facial Bones Мaxillae Anterior Nasal Spine Alveolar Processes Infraorbital Foramen Hard Palate Maxillary Sinus Palantine Nasal Inferior Nasal Conchae Zygomatic Temporal Process Lacrimal Vomer Mandible Body Ramus Angle Condylar Process Head - TMJ (Temporomandibular Joint) Coronoid Process Alveolar Processes Mental Protuberance Mental Foramen Mandibular Foramen

To get approved by the FDA generic drugs have to demonstrate the following: That their bio availability is the same as brand name drug That their bio equivalence is the same as the brand name drug That their bio availability AND bio equivalence is the same as the brand name drug None of the above

Explain the role of current Good Manufacturing practices (cGMP)  of manufacturing unit in pharmaceutical industries?  Please answer at your own easy words .

Please find the question

Please help me with 1 through 3, please.    1) In one or two sentences, restate the title of the paper in a way that would be understandable to a member of the general public without a scientific background. And when was the paper published as well as who funded the research? 2) Look at the citation at the beginning of the paper. Who is the first author of the paper?  And does this have any significance?  3)  Read the paper’s Abstract.  Summarize the main point of the study in two or three sentences.  (Make sure you use your own words).

which qualifies as “scientific evidence”?       It must have been validated and proven to be useful in court.   It must be free of any opportunity for bias and be repeatable.   It must be beyond a typical juror’s ability to understand and it must be relevant to the case.   It must be generally accepted by the relevant scientific community and have a known error rate.   It must be based on an approach that has been published in a peer-reviewed journal and have been validated.

Why should the procedures results of an experiment go through peer review

List and explain 5 ways animal test subjects be protected in research studies according to the Institutional Research Borad (IRB)?