Handbook of Pharmaceutical Manufacturing Formulations: Volume Five, Over-the-Counter Products PDF

Handbook of Pharmaceutical Manufacturing Formulations: Volume Five, Over-the-Counter Products PDF

Name:
Handbook of Pharmaceutical Manufacturing Formulations: Volume Five, Over-the-Counter Products PDF

Published Date:
12/17/2019

Status:
[ Active ]

Description:

Publisher:
CRC Press Books

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Czech version):
200 business days

SKU:
handbook-of-pharmaceutical-manufacturing-formulations-volume-five-over-the-counter-products_2844643

Choose Document Language:
82.50 €
Need Help?
ISBN: 9781351592352

The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Five, Over-the-Counter Products is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this fifth volume of a six-volume set, compiles data from FDA and EMA new drug applications, patents and patent applications, and other sources of generic and proprietary formulations including author’s own experience, to cover the broad spectrum of cGMP 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.

Features:

Largest source of authoritative and practical formulations, cGMP compliance guidance and self-audit suggestions

Differs from other publications on formulation science in that it focuses on readily scalable commercial formulations that can be adopted for cGMP manufacturing

Tackles common difficulties in formulating drugs and presents details on stability testing, bioequivalence testing, and full compliance with drug product safety elements

Written by a well-recognized authority on drug and dosage form development including biological drugs and alternative medicines

Author: Sarfaraz K. Niazi


Edition : 3
Number of Pages : 453
Published : 12/17/2019
isbn : 9781351592352

History


Related products


Best-Selling Products

SAA/SNZ HB 104:1997
Published Date: 01/01/1997
A guide to year 2000 compliance
28.12 €
SAA/SNZ HB 76:2010
Published Date: 08/19/2010
Dangerous Goods - Initial Emergency Response Guide
20.20 €
SAA/SNZ HB1:1994
Published Date: 10/17/1994
TECHNICAL DRAWING for students
8.71 €
SAA/SNZ HB18.43.1:1998
Published Date: 09/05/1998
Guidelines for third-party certification and accreditation Guide 43 - Proficiency testing by interlaboratory comparisons, Part 1: Development and operation of proficiency testing schemes
4.95 €
SAA/SNZ HB18.43.2:1998
Published Date: 09/05/1998
Guidelines for third-party certification and accreditation - Guide 43 - Proficiency testing by interlaboratory comparisons, Part 2: Selection and use of proficiency testing schemes by laboratory accreditation bodies
2.38 €
SAA/SNZ HB18.58:1993
Published Date: 01/01/1993
Guideline for third-party certification and accreditation, Part 58: Calibration and testing laboratory accreditation systems - General requirements for operation and recognition
2.38 €