We are excited to introduce the third edition of Validation of Pharmaceutical Processes. With the goal of ensuring pharmaceutical quality of the final manufactured product, the editors have introduced to the industry a subject so extensive that it impacts on good manufacturing practices, research and development, quality assurance, and facility design. Validation inevitably leads to process optimization, increased productivity, and lower costs in man-time and manufacturing. The objective of the third edition is to encompass the changes that have taken place in the pharmaceutical industry during the past several years. George Bernard Shaw once wrote that “science is always simple and always profound.
It is only the half-truths that are dangerous.”
The first and second editions of Validation of Pharmaceutical Processes, which filled the void of both aseptic and non-aseptic processes, are classics in the field of validation. The editors continue to build on the success of the previous books with significant updating of this third edition with information that must be made available in current practices. This new edition serves as a guide to validation methodologies for the preparation of all pharmaceutical products.clik here for download
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Pharmacovigilance is the science of collecting, monitoring, researching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications, biological products, herbalism and traditional medicines with a view to identifying new information about hazards associated with medicines and preventing harm to patients. Pharmacovigilance is particularly concerned with adverse drug reactions.The MHRA has identified a need for writing and publishing a guide to "Good Pharmacovigilance Practice". 
