Fundamentals of Pharmaceutical and Biologics Regulations...

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Fundamentals of Pharmaceutical and...

Fundamentals of Pharmaceutical and Biologics Regulations Volume I

Regulatory Affairs Professionals Society.

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This book gives you Overview of Regulatory Affairs.

ক্যাটাগোরিগুলো:

Science (General) - Research & Development

সাল:

2021

ভাষা:

english

ফাইল:

PDF, 3.95 MB

IPFS:

,

english, 2021

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তে রূপান্তর প্রক্রিয়া চলছে

-এ রূপান্তর ব্যর্থ হয়েছে

আপনি আগ্রহী হতে পারেন

RAPS — Fundamentals of US Regulatory Affairs, Eighth Edition

Javed Ali, Sanjula Baboota — Regulatory Affairs in the Pharmaceutical Industry

Various Authors — Global Pharmaceutical and Biologics Regulatory Strategy, Second Edition

REGULATORY AFFAIRS PROFESSIONALS SOCIETY — Fundamentals of EU Pharmaceutical and Biologics Regulations

Jack Wong, Raymond Tong — Medical Regulatory Affairs: An International Handbook for Medical Devices and Healthcare Products

Willig S. H. — Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality from Manufacturer to Consumer

Richard A. Guarino, Richard Guarino — New Drug Approval Process, , Accelerating Global Registrations

Shayne C. Gad — Regulatory Toxicology

Raj Bawa — Current immune aspects of biologics and nanodrugs - an overview

Ira R. Berry — Introduction to the Pharmaceutical Regulatory Process

Cohen, I. Glenn; Lynch, Holly Fernandez — FDA in the twenty-first century : the challenges of regulating drugs and new technologies

Holly Fernandez Lynch (editor); I. Glenn Cohen (editor) — FDA in the Twenty-First Century: The Challenges of Regulating Drugs and New Technologies

Dean E. Snyder (Editor) — FDA-Speak: A Glossary and Agency Guide

Smita Gopalaswamy (Author); Venky Gopalaswamy (Author) — Combination Products: Regulatory Challenges and Successful Product Development

Evan B. Siegel — Development and Approval of Combination Products: A Regulatory Perspective

Lionel D. Edwards, Andrew J. Fletcher, Anthony W. Fox, Peter D. Stonier — Principles and Practice of Pharmaceutical Medicine, Second Edition

Sandy Weinberg — Guidebook for Drug Regulatory Submissions

Sandy Weinberg — Cost-Contained Regulatory Compliance: For the Pharmaceutical, Biologics, and Medical Device Industries

John Griffin, John O'Grady — Regulation of Medical Products

Thomas M. Jacobsen, Albert I. Wertheimer — Modern Pharmaceutical Industry: A Primer

Richard A. Guarino — New Drug Approval Process

Richard A. Guarino — New Drug Approval Process Accelerating Global Registrations

Richard A. Rettig — The Acquisition of Drugs and Biologics for Chemical adn Biological Warfare Defense: Department of Defense Interactions with Food and DRug Administration

Food and Drug Administration — Compact Regs Parts 50, 54, 56, and 312: CFR 21 Parts 50, 56, and 312 Good Clinical Practices (10 Pack)

Whitmore, Elaine — Development of FDA-Regulated Medical Products - Prescription Drugs, Biologics, and Medical Devices

Whitmore, Elaine — Development of FDA-Regulated Medical Products: A Translational Approach, Second Edition

Susan Neadle — The Combination Products Handbook

Susan Neadle (editor) — The Combination Products Handbook: A Practical Guide for Combination Products and Other Combined Use Systems

Jeffrey S. Barrett — Fundamentals of Drug Development

Howard L. Dorfman — Pharmaceutical Compliance and Enforcement Answer Book 2016

Dean E Snyder — FDA-speak : a glossary and agency guide

Smita Gopalaswamy, Venky Gopalaswamy — Combination Products: Regulatory Challenges and Successful Product Development

R. Berry Ira, Robert P. Martin — The Pharmaceutical Regulatory Process

Douglas J. Pisano, David S. Mantus — FDA regulatory affairs : a guide for prescription drugs, medical devices, and biologics

Leon Shargel, Isadore Kanfer — Generic Drug Product Development: Solid Oral Dosage Forms, Second Edition

Richard A Guarino — New drug approval process

Laszlo Endrenyi, Dr. Paul Declerck, Shein-Chung Chow — Biosimilar Drug Product Development

Niazi, Sarfaraz — Biosimilars and interchangeable biologics: strategic elements

Sarfaraz K. Niazi — Biosimilar and Interchangeable Biologics: Strategic Elements

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