What you'll learn
Bioequivalence Study
Bioavailability
Generic Medicine Vs Branded Medicine
Bioequivalence study design
FDA Approval for Generics
Pharmacokinetics & Pharmacodynamics
Distinguish between Generics Vs Branded Medicines
Why generic medicines are cost effective
Pharma Clinical studies
Requirements
Pharmacy Background
Pharma Profession
Medical background required
Freshers & Experienced Professionals
Pharma Graduates / Post-Graduates
Research & Development
Pharmacy Clinical Knowledge
Description
Bioequivalence studies are very important for the development of a pharmaceutical preparation in the pharmaceutical industry. Their rationale is the monitoring of pharmacokinetic and pharmacodynamic parameters after the administration of tested drugs.Note: If you are paying more than 5k INR or $15 for private institute/academy then you are in loss. Please compare the course description and amount you are paying for such course.Bioavailability & BioequivalenceBioavailability (BA) is defined as the rate and extent to which the unchanged active substance is absorbed and becomes available in the systemic circulation. Understanding bioavailability is essential during drug development as it is one of the fundamental properties of drug formulation. Information on bioavailability is also used to determine bioequivalence (BE) when submitting a generic dossier.Through interactive sessions and multiple case studies, this course will evaluate every aspect of BA/BE from the regulations and types of protocol studies to bioanalysis, statistical analysis and reporting. Once completed you will have a solid understanding of bioavailability, supporting you in drug development. You will also have the confidence to develop and implement your own bioequivalence studies to ensure speedy generic approval.The course will also examine key aspects of biowaivers such as the regulatory hurdles, types of biowaivers and data needed so you can save money and time with fast biowaiver applications.Benefits of Course:After taking this course, students will be able to specify the design of a new drug or new device study with the goal of establishing whether the new protocol is statistically equivalent to an existing therapy. You will learn how to design a study in accordance with regulatory requirements, as well as appropriate methods for analyzing data. You will be able to fit statistical models to dose-response data with the goal of quantifying a reliable relationship between drug dosage and average patient response.Basic concepts for Bioequivalence studyBioavailability & bioequivalence Types of Study DesignsHow Generic medicine becomes Bioequivalent with Branded MedicinesCriteria and considerations for BA/BE StudyConduct PK analysis of time-concentration dataConduct dose-response analysisSpecify bioequivalence designs for parallel and crossover designsReview actual clinical trials and identify end point, question of interest, statistical method usedWho Should Take This CourseDiploma Pharmacy Students/ProfessorPharmacy StudentsPharmaceutical researcher, Investor, DoctorsMedical ProfessionalAnalysts responsible for designing, implementing or analyzing clinical trials.
Overview
Section 1: Course Overview
Lecture 1 Course Overview
Section 2: Introduction
Lecture 2 Introduction Part I
Lecture 3 Introduction Part II
Section 3: Pharmacokinetcs & Pharmacodynamics Concept
Lecture 4 Pharmacokinetics
Lecture 5 First Pass Effect (First pass Metabolism)
Section 4: Bioavailability & Bioequivalence
Lecture 6 Bioequivalence Overview
Lecture 7 Bioequivalence Basic Concept
Lecture 8 Bioequivalence Study
Section 5: GCP (Good Clinical Practices)
Lecture 9 Good Clinical Practices
Section 6: Rules and Protocols
Lecture 10 IRB (Investigational Review Board or ethics Committee)
Lecture 11 ICF (Inform Consent Form)
Section 7: Congratulations & Thank you
Lecture 12 Congratulations & Thank you
Pharmacy,Pharmacy Graduates Students,Pharmacy PG Diploma,Medical Students,Pharma Research Scientist,Pharma Professional,Formulator,Pharma Investors,BA/BE sponsors

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