Polymorphism in the Pharmaceutical Industry: Solid Form and Drug Development

 

"Polymorphism in the Pharmaceutical Industry - Solid Form and Drug Development" highlights the relevance of polymorphism in modern pharmaceutical chemistry, with a focus on quality by design (QbD) concepts. It covers all important issues by way of case studies, ranging from properties and crystallization, via thermodynamics, analytics and theoretical modelling right up to patent issues.

Pharmaceutical Drug Product Development and Process Optimization-Effective Use of Quality by Design

 

Pharmaceutical manufacturers are constantly facing quality crises of drug products, leading to an escalating number of product recalls and rejects. Due to the involvement of multiple factors, the goal of achieving consistent product quality is always a great challenge for pharmaceutical scientists. This volume addresses this challenge by using the Quality by Design (QbD) concept, which was instituted to focus on the systematic development of drug products with predefined objectives to provide enhanced product and process understanding.

Pharmaceutical Formulation: The Science and Technology of Dosage Forms

 

Formulation is a key step in the drug design process, where the active drug is combined with other substances that maximise the therapeutic potential, safety and stability of the final medicinal product. Modern formulation science deals with biologics as well as small molecules. Regulatory and quality demands, in addition to advances in processing technologies, result in growing challenges as well as possibilities for the field.

The art and science of dermal formulation development

 

The Art and Science of Dermal Formulation Development is a comprehensive guide to the theory and practice of transdermal and topical formulation development, covering preclinical studies, evaluation, and regulatory approval. It enables the reader to understand the opportunities and challenges in

Thẩm định thiết bị trong sản xuất dược phẩm (Equipment Qualification in the Pharmaceutical Industry)

Equipment Qualification in the Pharmaceutical Industry provides guidance and basic information for the preparation of a quality qualification program. It has been noted that there is a general lack of understanding in the industry, especially for those new to the industry, as to what constitutes a compliant qualification program. Even experienced professionals have felt a lack of security in reaching

Specification of Drug Substances and Products: Development and Validation of Analytical Methods

 

Specification of Drug Substances and Products: Development and Validation of Analytical Methods is a comprehensive and critical analysis of the requirements and approaches to setting specifications for new pharmaceutical products, with an emphasis on phase-appropriate development and validation of analytical methods. This book is intended as more than a review of new regional guidelines, existing regulatory guidance, and industry practices. It provides a hands-on guide to understanding and applying these in practice. The authors discuss critical issues, novel approaches, and future directions while also providing insight into how International Guidelines were developed and the rationale behind them.

Handbook of Pharmaceutical Manufacturing Formulations, Third Edition

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this six-volume set compiles data from FDA new drug applications, patent applications, and other sources of generic and proprietary formulations to cover the broad spectrum of GMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent

So sánh độ hòa tan của viên bao tan trong ruột

Điều kiện thử so sánh độ hòa tan của viên bao tan trong ruột được một số cơ quản lý quy định như sau: 

Hướng dẫn của ISPE: Thẩm định vệ sinh (Cleaning Validation)

This ISPE Guide: Cleaning Validation Lifecycle - Applications, Methods, and Controls provides a hands-on approach to support the life science industry in the development and establishment of compliant cleaning programs that meet or exceed regulatory expectations. Topics covered include:

Pharmaceutical Process Validation (Thẩm định quy trình sản xuất thuốc)

 1. Hướng dẫn của IVT (Institue of Validation Technology)

  a. Process design special edition (Stage 1)

  b. Process performance qualification special edition (Stage 2)

Bộ tài liệu hướng dẫn của ISPE (International Society for Pharmaceutical Engineering)

Các tài liệu hướng dẫn của ISPE được viết bởi các chuyên gia trong lĩnh vực sản xuất dược phẩm, sẽ cung cấp cho bạn những thông tin thực tế cần thiết để giúp công ty của mình xây dựng dựa trên các phương pháp tốt nhất để đáp ứng và vượt mức các tiêu chuẩn quy định bởi các cơ quan quản lý.

So sánh biểu đồ hòa tan - Biểu đồ hòa tan dao động nhiều

 

So Sánh Biểu Đồ Hòa Tan - Những Quy Định Khác Nhau Giữa Các Cơ Quan Quản Lý Trên Thế Giới

 

Thẩm định quy trình sản xuất dạng bào chế rắn đường uống - Solid oral dose process validation

 

British Pharmacopoeia 2018

Link tải: http://prereheus.com/1yhX

Handbook of Pharmaceutical Excipients 8th

Link tải: http://prereheus.com/1yO9