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Showing posts with label Validations. Show all posts
Showing posts with label Validations. Show all posts

Monday, August 16, 2010

Quality Assurance in Analytical Chemistry: Training and Teaching - Second edition

Bernd W. Wenclawiak, Michael Koch, Evsevios Hadjicostas

  • Publisher: Springer
  • Number Of Pages: 331
  • Publication Date: 2010-07-27
  • ISBN-10 / ASIN: 3642136087
  • ISBN-13 / EAN: 9783642136085


Product Description:

This new edition of a successful textbook has been completely revised and enlarged. In particular the chapters on measurement uncertainty, calibration and validation are practically all new. The authors provide an in-depth but easy to understand coverage of quality assurance for chemical measurements. This includes both internal as well as external quality assurance, necessary statistics as well as total quality management. All this is presented with more than 800 commented slides, which are also provided as downloadable Extra Material.

DOWNLOAD LINK:

http://mediafire.com/file/28k3znzuv8w4q0a/3642136087.pdf

http://ifile.it/mn2ethz/3642136087.pdf

Thursday, April 8, 2010

Useful Pharmaceutical Links

Analytical Method Development
Analytical Method Validation
Validated analytical method only can give accurate results. Validation of analytical method is must for pharmaceutical analytical laboratory.
There is guideline for analytical method validation from ICH & US FDA.
ICH-Q2(R1)- Validation of Analytical Procedures - Text and Methodology
US FDA draft guidance on analytical procedures & method validation
EDQM guideline

EDQM-Validation of analytical procedure

Analytical Method Transfer

There is no definite guidance from USFDA on this subject. Recently USP has come up with a stimuli article on this subject. For more information refer the link below.
Transfer of analytical procedures-A new general information chapter

Instrument calibration
1. Disolution Apparatus 1 & 2 - Mechanical calibration
2. Prednisone tablet for PVT - New lot - P1I303

Instrument Qualification

Annex 1: Qualification of HPLC Equipment

Annex 2: Qualification of GC Equipment

Annex 3: Qualification of UV-Visible Spectrophotometers

Annex 4: Qualification of IR Spectrophotometers


Result & Reports
Out-Of-Specification (OOS)
Investigation is must for any product failures to find out the root cause and Corrective And Preventive Action(CAPA). USFDA come up with definite guidance on this subject. This guideline helps to handle OOS data and procedure for investigation. For more information refer the below link.

Out-Of-Trend(OOT) Analytical Results
An analytical result which fall in with in the specification limit but does not follow with in the trend or unexpected result. Normally any analytical result which fall in Out-Of-Specification requires a detailed investigation to find a root cause failure and folowed by a currettive And Preventive Action(CAPA).
Though regulation demands investigation to be completed with in thirty days but most of the cases industries fails to complete the invsetigation with in stipulated period to find root cause.Meanwhile its end up with few more failures. To avoid such things happen the current practice starts investigation when results appear to be ou-of-trend.
The following links help to know more about OOT
Auditing pharmaceuticals quality control Laboratory

Auditing quality control laboratory is must for continuous improvement and regualotory requirements. It helps to keep QC laboratory in high compliance level and maintain best practices through continuos improvement by training and gap analysis.

There is a guideline from US FDA for inspection pharmaceuticals QC laboratory it

includes chemical lab and Micro lab.

Auditing Guide from APIC

Pharmaceutical Quality Control Labs

Audit check list for Pharmaceutical Quality Control Labs by PICScheme

Microbiological Pharmaceutical Quality Control Labs
Guidance document on part 11-Electronic signature & Electronic record

NEW: Annex 1: Validation of computerised calculation systems: example of validation of in-house software - Spread sheet/Microsoft Excel

NEW: Annex 2: Validation of Databases (DB), Laboratory Information Management Systems (LIMS) and Electronic Laboratory Notebooks (ELN)

NEW: Annex 3: Validation of computers as part of test equipment

GAMP 4 to GAMP 5 -Summary


Elemental Impurities—Comments and Responses (1.1MB)

Flow Microscopy—Dynamic Image Analysis for Particle Counting (1.1MB)

A Recombinant Factor C Procedure for the Detection of Gram-negative Bacterial Endotoxin (1.7MB)

High level list of Australian and International pharmaceutical regulations and standards

REGULATIONS

Australian


Australian Code of Good Manufacturing Practice for Medicinal Products – Therapeutics Goods Administration 16 August 2002.

Australian Code of Good Manufacturing Practice for Veterinary Chemical Products – Australian Pesticides & Veterinary Medicines Authority.

Australian Regulatory Guidelines for Complementary Medicines – Therapeutics Goods Administration June 2005.

Australian Medical Device Guidelines – Therapeutics Goods Administration

International

United States
Code of Federal Regulations 21CFR 210 - cGMP in Manufacturing, Processing, Packing, or holding of Drugs; General – U.S. Food & Drug Administration

Code of Federal Regulations 21CFR 211 cGMP for Finished Pharmaceuticals – U.S. Food & Drug Administration

Code of Federal Regulations 21CFR 600 - Biologics – U.S. Food & Drug Administration

Europe
Eudralex Volume 4 - Medicinal Products for Human and Veterinary Use : Good Manufacturing Practice – European Commission

Links to the Associations and Affiliations including general pharma, engineering, scientific and project management.

General Pharmaceutical

  • Pharmaceutical Inspection Cooperation Scheme (PIC/S)
    www.picscheme.org
  • World Health Organisation (WHO)
    www.who.int

  • Parental Drug Association (PDA) Home Page – Intramuscular and Intravenous drug news and information.
    www.pda.org


  • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) – scientific and technical aspects of product registration.
    www.ich.org


Engineering

  • International Society of Pharmaceutical Engineering (ISPE) Home Page – worlds largest non-profit professional organisation serving pharmaceutical and biotech manufacturing professionals.
    www.ispe.org
  • Engineers Australia Home Page – Revised and updated Institution of Engineers Australia (IEAust) Home Page. General information and news for all aspects of engineering in Australia.
    www.engineersaustralia.org.au


  • Association of Professional Engineers, Scientists and Managers, Australia (APESMA) Home Page
    www.apesma.asn.au

Scientific

  • Biospectrum Asia Home Page – Informative website on the pharma/biotech industries in Asia.
    www.biospectrumasia.com

  • Australia’s Biotechnology Organisation (Ausbiotech) Home Page – Australia wide biotechnology information website.
    www.ausbiotech.org
  • BioGeelong Home Page – News, links and information on the growing Geelong Biotechnology industry.
    www.biogeelong.com.au

Project Management

  • Project Management Institute (PMI) Home Page – Project Management resource website including standards, seminars, education programs and case studies.
    www.pmi.org

Others



Saturday, February 13, 2010

Introduction to Modern Liquid Chromatography, Third Edition

Introduction to Modern Liquid Chromatography, Third Edition.
By Lloyd R. Snyder, Joseph J. Kirkland, John W. Dolan

  • Publisher: Wiley
  • Number Of Pages: 912
  • Publication Date: 2009-12-09
  • ISBN-10 / ASIN: 0470167548
  • ISBN-13 / EAN: 9780470167540
Product Description:

The latest edition of the authoritative reference to HPLC

High-performance liquid chromatography (HPLC) is today the leading technique for chemical analysis and related applications, with an ability to separate, analyze, and/or purify virtually any sample. Snyder and Kirkland's Introduction to Modern Liquid Chromatography has long represented the premier reference to HPLC. This Third Edition, with John Dolan as added coauthor, addresses important improvements in columns and equipment, as well as major advances in our understanding of HPLC separation, our ability to solve problems that were troublesome in the past, and the application of HPLC for new kinds of samples.

This carefully considered Third Edition maintains the strengths of the previous edition while significantly modifying its organization in light of recent research and experience. The text begins by introducing the reader to HPLC, its use in relation to other modern separation techniques, and its history, then leads into such specific topics as:

  • The basis of HPLC separation and the general effects of different experimental conditions
  • Equipment and detection
  • The column—the "heart" of the HPLC system
  • Reversed-phase separation, normal-phase chromatography, gradient elution, two-dimensional separation, and other techniques
  • Computer simulation, qualitative and quantitative analysis, and method validation and quality control
  • The separation of large molecules, including both biological and synthetic polymers
  • Chiral separations, preparative separations, and sample preparation
  • Systematic development of HPLC separations—new to this edition
  • Troubleshooting tricks, techniques, and case studies for both equipment and chromatograms
Designed to fulfill the needs of the full range of HPLC users, from novices to experts, Introduction to Modern Liquid Chromatography, Third Edition offers the most up-to-date, comprehensive, and accessible survey of HPLC methods and applications available.

DOWNLOAD LINK:

Sunday, November 29, 2009

Handbook of Drug Screening, Second Edition (Drugs and the Pharmaceutical Sciences) By Ramakrishna Seethala, Litao Zhang

Handbook of Drug Screening, Second Edition (Drugs and the Pharmaceutical Sciences)
By Ramakrishna Seethala, Litao Zhang.


  • Publisher: Informa Healthcare
  • Number Of Pages: 504
  • Publication Date: 2009-06-24
  • ISBN-10 / ASIN: 1420061682
  • ISBN-13 / EAN: 9781420061680
Product Description:

Building upon the foundation of basics discussed in the previous edition, the Second Edition provides a more in-depth look at the latest methods and technologies of advanced drug screening, an essential function of drug discovery.


With extensively updated content and 21 new chapters, this text examines:

quality and efficiency of drug target validation and potential drug compound selection
reducing assay costs and improvement in assay technology
data quality improvement
trends in drug discovery
how drug screening can minimize adverse drug effects
recent advancements, including: high content screening; protein-protein interactions; high-throughput crystallization; lead optimization; chemoinformatics and microfluidics technologies; target validation by genomics, proteomics, and siRNA; structure-based drug design; automation; and medicinal chemistry.

DOWNLOAD LINK:

Friday, August 7, 2009

Rapid Microbiological Methods in the Pharmaceutical Industry


In recent years there has been increased interest in the possibility of rapid microbiological methods offering enhanced potential error detection capabilities. However, these methods raise a number of questions, such as how to validate new methods, will they be accepted by the pharmacopoeias, and, most importantly, how will the regulators respond? Rapid Microbiological Methods in the Pharmaceutical Industry answers these questions and more. Martin Easter and his panel of experts: § Describe the range of rapid microbiological methods and their applications, including practical tips, and their status regarding validation, established use, and regulatory acceptance § Explore the origins of current methods and the current issues facing the requirements of microbiology and its associated test methods § Delineate the challenges involved in seeking better and more pragmatic methods for the assessment of microbial hazards and risks to ensure product and consumer safety The book assists you in applying an effective system to assess the real microbiological hazards and, hence, quantify realistic risks. Additionally, it provides monitoring methods that will deliver meaningful, useful data for effective decision making in manufacturing, quality assurance, and product safety. The expert and authoritative information in Rapid Microbiological Methods in the Pharmaceutical Industry will help you find better solutions to ensuring the microbiological safety of pharmaceutical products.

Download:-http://rapidshare.com/files/144839279/trapmicro_meth_pharma_ind.zip

Thursday, July 23, 2009

Sterilization Validation and Routine Operation Handbook: Radiation


Sterilization Validation and Routine Operation Handbook: Radiation.
CRC | April 4, 2001 | 168 pages | ISBN-10 / ASIN : B001DBI1K6 | PDF | 5.1mb

The validation and radiation sterilization process for biomaterials and medical devices requires careful planning to ensure regulatory compliance followed by precise accuracy in execution and documentation. This in-depth guide details all steps from prevalidation planning to final report and ongoing monitoring and control. Sterilization Validation & Routine Operation Handbook: Radiation provides a framework for the validation and routine operation of an irradiation sterilization process. The guidance presented complies with ANSI/AAMI/ISO 11137: 1994, Sterilization of health care product-Requirements for validation and routine control-Radiation sterilization and the newly published AAMI substantiation of 25 kGy using VDmax procedure. The author discusses methods to aid in comprehending the requirements in these standards. She also provides practical procedures for the validation and routine monitoring and control of specific gamma and electron beam radiation sterilization processes.Background chapters provide needed information on radiation sterilization technologies, sterilization microbiology, validation approaches and working with a radiation sterilization contractor. Much of the information in this new book is presented in convenient tables and charts, with diagrams and other schematics that simply illustrate appropriate validation methodologies. Sterilization Validation & Routine Operation Handbook: Radiation brings together in one resource information scattered throughout many documents and will be useful to all those involved in the sterilization of medical materials, drugs and devices.

DOWNLOAD LINK:


Wednesday, July 15, 2009

Rapid Microbiological Methods in the Pharmaceutical Industry by Martin C. Easter


Rapid Microbiological Methods in the Pharmaceutical Industry by Martin C. Easter.
Publisher: CRC Press | March 19, 2003 | ISBN: 1574911414 | Pages: 288 | PDF | 2.76 MB

In recent years there has been increased interest in the possibility of rapid microbiological methods offering enhanced potential error detection capabilities. However, these methods raise a number of questions, such as how to validate new methods, will they be accepted by the pharmacopoeias, and, most importantly, how will the regulators respond? Rapid Microbiological Methods in the Pharmaceutical Industry answers these questions and more.Martin Easter and his panel of experts:§Describe the range of rapid microbiological methods and their applications, including practical tips, and their status regarding validation, established use, and regulatory acceptance§Explore the origins of current methods and the current issues facing the requirements of microbiology and its associated test methods§Delineate the challenges involved in seeking better and more pragmatic methods for the assessment of microbial hazards and risks to ensure product and consumer safety The book assists you in applying an effective system to assess the real microbiological hazards and, hence, quantify realistic risks. Additionally, it provides monitoring methods that will deliver meaningful, useful data for effective decision making in manufacturing, quality assurance, and product safety. The expert and authoritative information in Rapid Microbiological Methods in the Pharmaceutical Industry will help you find better solutions to ensuring the microbiological safety of pharmaceutical products.

DOWNLOAD LINK:

Monday, July 13, 2009

Analytical Molecular Biology



G. Saunders, H. Parkes, "Analytical Molecular Biology".
Royal Society of Chemistry | 1999-03-30 | ISBN: 0854044728 | 200 pages | PDF | 15,4 MB

Introduces the issues of validation and quality to the bioanalytical community, specifically addressing DNA-based analyses. Designed to raise awareness of the factors that can influence the validity of DNA analysis and the production of additional challenges that are associated with the analysis of real samples. Spiral.

DOWNLOAD LINK:

Saturday, July 11, 2009

Quality Assurance and Quality Control in the Analytical Chemical Laboratory: A Practical Approach (Analytical Chemistry)


Quality Assurance and Quality Control in the Analytical Chemical Laboratory: A Practical Approach (Analytical Chemistry).
Publisher: CRC | ISBN: 1420082701 | edition 2009 | PDF | 232 pages | 2,17 mb
Using an approach grounded in hands-on experience, the book
begins with the theory behind quality control systems and then moves on to discuss examples of such tools as validation parameter measurements, the use of statistical tests, counting the margin of error, and estimating uncertainty. The authors draw on their experience in uncertainty estimation, traceability, statistics, proficiency tests, and method validation to craft a resource that provide practical guidance for each step of the quality assurance process.

DOWNLOAD LINK:

Thursday, June 18, 2009

British National Formulary 57: March 2009

British National Formulary 57: March 2009.
By Joint Formulary Committee
  • Publisher: Pharmaceutical Press
  • Number Of Pages: 978
  • Publication Date: 2009-04-02
  • ISBN-10 / ASIN: 0853698457
  • ISBN-13 / EAN: 9780853698456
Product Description:

This is the authoritative guide to prescribing, dispensing and administering medicines for all health care professionals. Nobody working in health care can afford to be without the latest edition of "BNF". Compiled with the advice of clinical experts and continually updated to reflect the latest evidence from all credible sources worldwide, this essential reference provides up-to-date guidance on prescribing, dispensing, administering, and monitoring medicines. Not only does the "BNF" include the widely accepted framework for the drug management of common diseases, it also includes details of medicines prescribed in the UK, with special reference to their uses, cautions, contraindications, side-effects, dosage and relative costs. This allows treatment to be tailored to the individual needs of each patient. Updated in print every six months by an expert team of pharmacists, with guidance and validation from a network of leading clinicians, and oversight by a Joint Formulary Committee with representatives from all spheres of clinical practice. "The BNF" reflects current best practice as well as legal and professional guidelines relating to the use of medicines. As a result it is used widely as a touchstone reference, and cited in Parliaments and courts as a source of authority. This title is available online as part of MedicinesComplete, on PDA and on CD-ROM for intranets.

DOWNLOAD LINK:

http://rapidshare.com/files/242830701/tbnf57t.zip

Wednesday, May 20, 2009

Quality Assurance and Quality Control in the Analytical Chemical Laboratory: A Practical Approach (Analytical Chemistry)

Quality Assurance and Quality Control in the Analytical Chemical Laboratory: A Practical Approach (Analytical Chemistry).
By Piotr Konieczka, Jacek Namiesnik
  • Publisher: CRC
  • Number Of Pages: 232
  • Publication Date: 2009-02-23
  • ISBN-10 / ASIN: 1420082701
  • ISBN-13 / EAN: 9781420082708

Product Description:

Using an approach grounded in hands-on experience, the book begins with the theory behind quality control systems and then moves on to discuss examples of such tools as validation parameter measurements, the use of statistical tests, counting the margin of error, and estimating uncertainty. The authors draw on their experience in uncertainty estimation, traceability, statistics, proficiency tests, and method validation to craft a resource that provide practical guidance for each step of the quality assurance process.

DOWNLOAD LINK:
http://ifile.it/dl

Thursday, April 30, 2009

Good Design Practices for GMP Pharmaceutical Facilities

0824754638

Good Design Practices for GMP Pharmaceutical Facilities (Drugs and the Pharmaceutical Sciences): Andrew Signore, Terry Jacobs
Informa HealthCare | ISBN: 0824754638 | June 10, 2005 | PDF (OCR) | 576 pages | 18022 KB

A convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern pharmaceutical facilities, this guide assists project managers as they develop, diagram, and implement pharmaceutical production facility projects-demonstrating how advances in technology and external regulation can impact the production and efficacy of a pharmaceutical facility and the products it produces.

DOWNLOAD LINK:
Rapidshare.com

Tuesday, April 28, 2009

International IT Regulations and Compliance: Quality Standards in the Pharmaceutical and Regulated Industries

International IT Regulations and Compliance: Quality Standards in the Pharmaceutical and Regulated Industries.
By Siri H. Segalstad

  • Publisher: Wiley-Blackwell (an imprint of John Wiley & Sons L
  • Number Of Pages: 338
  • Publication Date: 2008-12-15
  • ISBN-10 / ASIN: 0470758821
  • ISBN-13 / EAN: 9780470758823
Product Description:
Standards, technologies, and requirements for computer validation have changed dramatically in recent years, and so have the interpretation of the standards and the understanding of the processes involved. International IT Regulations and Compliance brings together current thinking on the implementation of standards and regulations in relation to IT for a wide variety of industries. The book provides professionals in pharmaceutical and semiconductor industries with an updated overview of requirements for handling IT systems according to various Quality Standards and how to ?translate? these requirements in the regulations.

DOWNLOAD LINK:
http://rapidshare.com/files/220859065/0470758821.zip

Monday, April 27, 2009

Analytical Method Development and Validation by Michael E. Swartz


Analytical Method Development and Validation by Michael E. Swartz (Editor), Ira S. Krull (Editor)
Publisher: CRC Press | 16 May 1997 | ISBN: 0824701151 | Pages: 96 | PDF | 4.2 MB

." . .a useful primer-type book covering validation of analytical methods. . . .recommended." ---Analyst "Stop and read this. . .book to understand a formal way to develop or to improve and validate your methods. . .. In answer to any query posed to you about your methods development technique, you could hand your well-worn copy of this small book to the questioner. There should be no further questions." ---INFORM

Describes analytical methods development, optimization and validation, and provides examples of successful methods development and validation in high-performance liquid chromatography (HPLC) areas. The text presents an overview of Food and Drug Administration (FDA)/International Conference on Harmonization (ICH) regulatory guidelines, compliance with validation requirements for regulatory agencies, and methods validation criteria stipulated by the US Pharmacopia, FDA and ICH.

DOWNLOAD LINK:
Mirror


Sunday, April 19, 2009

Fragment-Based Drug Discovery: A Practical Approach


Edward Zartler, Michael Shapiro, “Fragment-Based Drug Discovery: A Practical Approach.”
Wiley | 2008-12-31 | ISBN: 0470058137 | 296 pages | PDF | 3,4 MB

Fragment-based drug discovery (FBDD) is a new paradigm in drug discovery that utilizes very small molecules - fragments of larger molecules. It is a faster, cheaper, smarter way to do drug discovery, as shown by the number of pharmaceutical companies that have embraced this approach and the biotechnology companies who use fragments as their sole source of drug discovery.

Fragment-Based Drug Discovery: A Practical Approach is a guide to the techniques and practice of using fragments in drug screening. The emphasis is on practical guidance, with procedures, case studies, practical tips, and contributions from industry. Topics covered include:
an introduction to fragment based drug discovery, why using fragments is a more efficient process than predominant models, and what it means to have a successful FBDD effort.
setting up an FBDD project
library building and production
NMR in fragment screening and follow up
application of protein-ligand NOE matching to the rapid evaluation of fragment binding poses
target immobilized NMR screening: validation and extension to membrane proteins
in situ fragment-based medicinal chemistry: screening by mass spectrometry
computational approaches to fragment and substructure discovery and evaluation
virtual fragment scanning: current trends, applications and web based tools
fragment-based lead discovery using covalent capture methods
case study from industry: the identification of high affinity beta-secretase inhibitors using fragment-based lead generation

With contributions from industry experts who have successfully set up an industrial fragment-based research program, Fragment-Based Drug Discovery: A Practical Approach offers essential advice to anyone embarking on drug discovery using fragments and those looking for a new approach to screening for drugs.

DOWNLOAD LINK:
http://rapidshare.com/files/182096612/Fragment_Based_Drug_Discovery.rar

Monday, April 13, 2009

International IT Regulations and Compliance: Quality Standards in the Pharmaceutical and Regulated Industries

International IT Regulations and Compliance: Quality Standards in the Pharmaceutical and Regulated Industries.
By Siri H. Segalstad
  • Publisher: Wiley-Blackwell (an imprint of John Wiley & Sons L
  • Number Of Pages: 338
  • Publication Date: 2008-12-15
  • ISBN-10 / ASIN: 0470758821
  • ISBN-13 / EAN: 9780470758823
Product Description:

Standards, technologies, and requirements for computer validation have changed dramatically in recent years, and so have the interpretation of the standards and the understanding of the processes involved. International IT Regulations and Compliance brings together current thinking on the implementation of standards and regulations in relation to IT for a wide variety of industries. The book provides professionals in pharmaceutical and semiconductor industries with an updated overview of requirements for handling IT systems according to various Quality Standards and how to ?translate? these requirements in the regulations.

Sunday, April 12, 2009

Validation in Chemical Measurement


Validation in Chemical Measurement by: Paul De BiFvre Helmut Gnnzler
Publisher: Springer | ISBN: 3540207880 | 2005-01-12 | Pages: 186 | PDF | 3 MB

The validation of analytical methods is based on the characterisation of a measurement procedure (selectivity, sensitivity, repeatability, reproducibility). This volume collects 31 outstanding papers on the topic, mostly published in the period 2000-2003 in the journal "Accreditation and Quality Assurance". They provide the latest understanding, and possibly the rationale why it is important to integrate the concept of validation into the standard procedures of every analytical laboratory. In addition, this anthology considers the benefits to both: the analytical laboratory and the user of the measurement results.

DOWNLOAD LINK:
http://depositfiles.com/en/files/m9uysl80e

Saturday, March 28, 2009

Handbook of Ion Chromatography((Once again posted)

Handbook of Ion Chromatography.
Product Details
  • Hardcover: 931 pages
  • Publisher: Wiley-VCH; 3 Rev Upd edition (January 4, 2005)
  • Language: English
  • ISBN-10: 3527287019
  • ISBN-13: 978-3527287017
  • Product Dimensions: 9.9 x 7.2 x 2.4 inches
Book Description
The third edition of this highly successful and established handbook has been completely revised and considerably extended, making it unrivaled in the timeliness and comprehensiveness of the information presented. This new edition runs to two volumes, with added chapters or sections covering:
- New and important applications of ion chromatography in the life sciences, such as the analysis of proteins, nucleic acids, amino acids or carbohydrates.
- New instrumentation that meets the demand for miniaturization and reduced analysis times.
- Coupling of ion chromatography to mass-spectrometric or inductively coupled plasma detectors
- Validation of ion-chromatographic methods, which is important for quality assurance
The author has played a major role in the development of ion chromatography and – alongside his industrial post -- has been appointed as visiting professor at the University of Innsbruck, one of the prominent centers of chromatography research in the world.

DOWNLOAD LINK:
http://rs134.rapidshare.com/files/107723184/H098.rar

Rapid Microbiological Methods in the Pharmaceutical Industry

Rapid Microbiological Methods in the Pharmaceutical Industry.

By Martin C. Easter

Publisher: CRC
Number Of Pages: 288
Publication Date: 2003-03-19
Binding: Hardcover

Product Description

In recent years there has been increased interest in the possibility of rapid microbiological methods offering enhanced potential error detection capabilities. However, these methods raise a number of questions, such as how to validate new methods, will they be accepted by the pharmacopoeias, and, most importantly, how will the regulators respond? Rapid Microbiological Methods in the Pharmaceutical Industry answers these questions and more. Martin Easter and his panel of experts: § Describe the range of rapid microbiological methods and their applications, including practical tips, and their status regarding validation, established use, and regulatory acceptance § Explore the origins of current methods and the current issues facing the requirements of microbiology and its associated test methods § Delineate the challenges involved in seeking better and more pragmatic methods for the assessment of microbial hazards and risks to ensure product and consumer safety The book assists you in applying an effective system to assess the real microbiological hazards and, hence, quantify realistic risks. Additionally, it provides monitoring methods that will deliver meaningful, useful data for effective decision making in manufacturing, quality assurance, and product safety. The expert and authoritative information in Rapid Microbiological Methods in the Pharmaceutical Industry will help you find better solutions to ensuring the microbiological safety of pharmaceutical products. Features

or
http://xinio.info/?http://ifile.it/zxugm0t/1574911414.zip
or
http://rapidshare.com/files/144839279/trapmicro_meth_pharma_ind.zip

Wednesday, March 4, 2009

Real World Drug Discovery: A Chemist's Guide to Biotech and Pharmaceutical Research

Real World Drug Discovery: A Chemist's Guide to Biotech and Pharmaceutical Research.
By Robert M. Rydzewski
  • Publisher: Elsevier Science
  • Number Of Pages: 512
  • ISBN-10 / ASIN: 0080466176
  • ISBN-13 / EAN: 9780080466170
Product Description:

Drug discovery increasingly requires a common understanding by researchers of the many and diverse factors that go into the making of new medicines. The scientist entering the field will immediately face important issues for which his education may not have prepared him: project teams, patent law, consultants, target product profiles, industry trends, Gantt charts, target validation, pharmacokinetics, proteomics, phenotype assays, biomarkers, and many other unfamiliar topics for which a basic understanding must somehow be obtained. Even the more experienced scientist can find it frustratingly difficult to get an overview of the many factors involved in modern drug discovery and often only after years of exploring does a whole and integrated picture emerge in the mind of the researcher.

Real World Drug Discovery: A Chemists Guide to Biotech and Pharmaceutical Research presents this kind of map of the landscape of drug discovery. In a single, readable volume it outlines processes and explains essential concepts and terms for the recent science graduate wondering what to expect in pharma or biotech, the medicinal chemist seeking a broader and more timely understanding of the industry, or the contractor or collaborator whose understanding of the commercial drug discovery process could increase the value of his contribution to it.

Key Features:

- Interviews with well-known experts in many of the fields involved, giving insightful comments from authorities on many of the sub-disciplines important to cutting edge drug discovery.

- Helpful suggestions gleaned from years of experience in biotech and pharma, which represents a repository drug discovery "lore" not previously available in any book.

- "Periodic Table of Drugs" listing current top-selling drugs arranged by target and laid out so that structural similarities and differences are plain and clear, with regular updates available at the book's website.

- Extensive use of diagrams to illustrate concepts like biotech startup models, preteomic profiling for target identification, Gantt charts for project planning, etc.

DOWNLOAD LINK: