P P Sharma Cosmetics Books Pdf
PDF Cosmetics are incredibly in demand since historical time. Leonard Hill books and Intertext p. Sharma, Cosmetics - Formulation, manufacturing. And quality control. =) = 8 1 0 002 68 1, correct to 3 signi cant gures. C Again, the time interval has been altered. Now the appropriate value for is 2. Let W be the number of demands in 15 minutes. P P 1e e4 6 22 W2 1!! =) 2 + e 2 P) (2 0 2 1 00 4 01, correct to 3 signi cant gures. Here is a summary of the results of this section. P P Sharma Cosmetic Formulation Book Free Download cosmetic formulation by pp sharma pdf DOWNLOAD (P P Sharma Cosmetic Formulation Book Free LINK Download on hongbermickrac P P Sharma Cosmetic Formulation Book Free LINK Download. COSMETICS: Formulation, manufacturing and Quality Control Fifth Ed., 2014 by P.P. Sharma 936 Pages, Hardcover In the Intervening years since the last edition of the Book was published, there have been changes in the regulations. The Indian Standard IS 4707 (Part 2 ) has been revised and many raw materials have.
Validation in Pharmaceutical Industry authored by senior regulatory officer of Delhi Govt. was published in 2007. Validation is a part of Good Manufacturing Practices (GMPs). This element of GMPs is most enquired aspect during the regulatory inspections. All GMP texts, national, regional and international have this element. Validation element, under the GMP, include qualification on facilities, equipment and utilities and process validation.
In this title, the author has dwelled upon concepts, options and validation of different processes. Documentation is an essential requirement of GMP. Validation documentation assumes importance because of its necessity for repeated intended performance of the process. Documentation like Validation Master Plan (VMP), qualification documentation (DQ,IQ,OQ, PQ), validation protocol, ETOP, change control documents have been explained.
Since statistical formulae are used in handling data generated during validation experiments, a chapter has been included in the book on statistical principles and tools used in validation and quality control of drugs.
There are chapters on qualification of facilities including HVAC, utilities like water, steam, validation of special processes like aseptic process, lyophilization. Now a day, computers are used to regulate processes, therefore, a chapter has been included on computer system validation.
The book has been reviewed and updated and three new chapters have been added in the second edition of this book which has been published in 2013. Highlights of the second edition are:
Three new chapters added, the following
- Calibration and Qualification
- Validation of Packaging Operations
- Process Validation and Medical Devices
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Texts of all chapters of first edition reviewed and updated
Guidance formats included for
- Qualification and Validation Protocols
- Change Control
- Qualification Matrix
- Control Charts
Indian GMP , WHO GMP, US FDA cGMP, Supplementary GMPs, PAT HACCP, ICH Q10 CAPA, QRM QbD ICH Q8
The book, How to Practice GMPs authored by P.P.Sharma, senior regulatory officer of the Drugs Control Department of Government of Delhi was first published in 1991 after incorporation of GMPs under Schedule M to the Drugs and Cosmetics Rules, 1945. It was the first book in India on GMP. The book has been reviewed regularly by the author and subsequent editions appeared in the years mentioned below:
Second edition 1995
Third edition 2001
Fourth edition 2004
Fifth edition 2006
Sixth edition 2010
Seventh edition 2015
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The current edition is the seventh edition. While updating the book, author has taken in to consideration various supplementary GMP guidelines published by WHO and EU Guidance on GMP.
Highlights of 7th Ed. :
- Two New Chapters have been added
- Pharmaceutical Development has been covered
- Principles of QbD added
- ICH & WHO Guidelines on QRM included
- GMP guidelines on medicinal gases added
- Revised WHO GMP guidelines on API and sterile products included
- Entire text of the book reviewed and updated
ICH has published ICH Q10 which is a document on Pharmaceutical Quality System. Participating countries of ICH are in the process of incorporating the systems mentioned in the document in their regulations. CAPA (Corrective Action and Preventive Action) system is an element of both ICH Q10 as well as ISO:9000. Overview of ICH Q10 and CAPA system has been included.
Amongst the appendices, the book has texts of Indian GMP, WHO GMP, US FDA GMP.X