Guideline for Bioequivalence Studies for Different Strengths of Oral Solid Dosage Forms
Study of regulatory requirements for the conduct of bioequivalence studies in US, Europe, Canada, India, ASEAN and SADC countrie
ETHICAL GUIDELINES AND STUDY DESIGN FOR BIOAVAILABILITY AND BIOEQUIVALENCE STUDY
7. Clinical Trial Assessment Bioequivalent Studies（Generic)
ETHICAL GUIDELINES AND STUDY DESIGN FOR BIOAVAILABILITY AND BIOEQUIVALENCE STUDY | Semantic Scholar
Japan | SpringerLink
Pharmacogenetic perspectives in improving pharmacokinetic profiles for efficient bioequivalence trials with highly variable drugs: a review | International Journal of Pharmacokinetics
Clinical Protocol Development: Bioequivalence Generic Products - BioPharma Services
Bioequivalence of topical generic products. Part 2. Paving the way to a tailored regulatory system - ScienceDirect
Myths, questions, facts about generic drugs in the EU - GaBI Journal
Guideline for Bioequivalence Studies of Generic Products 発医薬品の生物学的同等性試験ガイドライン
GENERIC DRUGS: Guidelines for bioequivalence studies: Vishwakarma, Pushpendra Kumar: 9783639343779: Amazon.com: Books
Article|International Journal of Current Research and Review
Guideline for Bioequivalence Studies of Generic Products
GENERIC DRUGS: Guidelines for bioequivalence studies: Vishwakarma, Pushpendra Kumar: 9783639343779: Amazon.com: Books
PDF) International Guidelines for Bioequivalence of Systemically Available Orally Administered Generic Drug Products: A Survey of Similarities and Differences
Current regulatory scenario and alternative surrogate methods to establish bioequivalence of topical generic products - ScienceDirect
Japan | SpringerLink
Current set of major guidelines for bioequivalence studies in Japan... | Download Table
15.6 Choice of the reference product for bioequivalence of generic medicines | Therapeutic Goods Administration (TGA)
PPT - Bioequivalence studies: Regulatory Requirements on Conduct & Documentation of BE. PowerPoint Presentation - ID:5123884
Guideline o the Investigation of Bioequivalence
Pharmaceutics | Free Full-Text | In Vitro Dissolution and in Silico Modeling Shortcuts in Bioequivalence Testing | HTML
A pragmatic regulatory approach for complex generics through the U.S. FDA 505(j) or 505(b)(2) approval pathways - Klein - 2021 - Annals of the New York Academy of Sciences - Wiley Online Library
Egyptian Guidelines For the Conduct of Bioequivalence Studies
regulatory requirement for bioequivalence
