Pharmaceutical Clinical Bioequivalence Study (BA/BE) | Udemy

Pharmaceutical Clinical Bioequivalence Study (BA/BE) For two days completely 100% Free during everything you want to know bout Clinical Bioequivalence Study, BABE, Types of Study designs, Crossover Design, Parallel Design, AUC, Cmax, Tmax, PK/PD

This course is written by the very popular author from Udemy Mahesh Pratapwar The most Last updated 2/2022. The language of this course is English 🇺🇸, but also has subtitles (captions) in English [US] languages to better understand. This course is shared under the categories Teaching & Academics, Science, Pharmacy.

More than 1,423 students had already enrolled. in the Pharmaceutical Clinical Bioequivalence Study (BA/BE) | Udemy Which makes it one of the more popular courses on Udemy. You can free coupon Code the course from the registration link below. It has a rating of 3.9 given by  (18 ratings), which also makes it one of the highest-rated courses at Udemy. 

The Udemy Pharmaceutical Clinical Bioequivalence Study (BA/BE) free coupons also 4 hours on-demand video, 3 articles, 10 downloadable, resources, full lifetime, access on mobile and television, assignments, completion certificate and many more.

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Is this course right for you?

If you are wondering what you will learn or what things this best Udemy courses  will teach you after getting courses Udemy free coupon. Learn Pharmaceutical Clinical Bioequivalence Study (BA/BE) | Udemy: Okay, here are a few things.

• Pharmacy
• Pharmacy Graduates Students
• Pharmacy PG Diploma
• Medical Students
• Pharma Research Scientist
• Pharma Professional
• Formulator
• Pharma Investors
• BA/BE sponsors

Requirements Course:

1. Pharmacy Background
2. Pharma Profession
3. Medical background required
4. Freshers & Experienced Professionals
5. Pharma Graduates / Post-Graduates
6. Research & Development
7. Pharmacy Clinical Knowledge

Description Course:

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.

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Bioavailability & Bioequivalence

Bioavailability (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 study
• Bioavailability & bioequivalence
• Types of Study Designs
• How Generic medicine becomes Bioequivalent with Branded Medicines
• Criteria and considerations for BA/BE Study
• Conduct PK analysis of time-concentration data
• Conduct dose-response analysis
• Specify bioequivalence designs for parallel and crossover designs
• Review actual clinical trials and identify end point, question of interest, statistical method used

Who Should Take This Course

Diploma Pharmacy Students/Professor

Pharmacy Students

Pharmaceutical researcher, Investor, Doctors

Medical Professional

Analysts responsible for designing, implementing or analyzing clinical trials.

What I am going to 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

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