Pharmaceutical Technology

Microarrays play an increasingly significant role in drug discovery. The commercial landscape has changed dramatically over the past few years and ...

Microarrays play an increasingly significant role in drug discovery. The commercial landscape has changed dramatically over the past few years and ...

The preparation of sterile products using aseptic processing is considered perhaps the most critical process in the pharmaceutical industry and has...

The preparation of sterile products using aseptic processing is considered perhaps the most critical process in the pharmaceutical industry and has...

Dietary Supplement GMP is a one-stop how-to road map to the final dietary supplement GMP regulations recently issued by the FDA covering the manufa...

Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality teaches the basic principles of the development and manufacture of high q...

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Five, Over-the-Counter Products is an authoritative and practical ...

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Four, Semisolid Products is an authoritative and practical guide t...

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume One, Compressed Solid Products is an authoritative and practical g...

Already popular in the analysis of medical device trials, adaptive Bayesian designs are increasingly being used in drug development for a wide vari...

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Three, Liquid Products is an authoritative and practical guide to ...

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Two, Uncompressed Solid Products is an authoritative and practical...

As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In rec...

As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In rec...

Are herbal drugs totally devoid of adverse effects when used alone, as herbal formulations, or in concurrent use with modern medicines? Safety Conc...

Are herbal drugs totally devoid of adverse effects when used alone, as herbal formulations, or in concurrent use with modern medicines? Safety Conc...

Are herbal drugs totally devoid of adverse effects when used alone, as herbal formulations, or in concurrent use with modern medicines? Safety Conc...

An ideal drug candidate should possess good pharmacological activity, absorption, distribution, metabolism, excretion and toxicity properties. Hist...

Thoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and ver...

The rapid advances in recombinant DNA technology and the increasing availability of peptides and proteins with therapeutic potential are a challeng...

FDA Regulatory Affairs is a roadmap to prescription drug, biologics, and medical device development in the United States. Written in plain English,...

In this era of increased pharmaceutical industry competition, success for generic drug companies is dependent on their ability to manufacture thera...

The concept of frailty offers a convenient way to introduce unobserved heterogeneity and associations into models for survival data. In its simples...

There are more than 500 biopharmaceuticals on the market, including more than 200 therapeutic proteins, making biologics the fastest growing sector...