GBI Research's report, "Manufacturing of Solid Dosage Forms - 2011"" Production Capacity May Force Regulatory Bodies to Re-Design Guidelines on Quality Standards". The report provides the key market data on the Contract Manufacturing Organization (CMO) market size for solid dosage forms along with forecast from 2009-2016 for API and excipient market. The report also gives insight into challenges, unmet needs, and technology landscape and cGMP guidelines for manufacturing of solid dosage forms. The report also analyzes the strengths, weaknesses, opportunities, and threats leading players involved in manufacturing of solid dosage forms. The report is based on proprietary databases, primary and secondary research and in-house analysis by GBI Research's team of industry experts to provide a comprehensive view of the manufacturing of solid dosage forms.

The proper design and formulation of a solid dosage form requires knowledge about the physical, chemical and biological distinctiveness of pharmaceutical ingredients (API and excipients) to be used in manufacturing process. GBI research estimates that the APIs market was will grow from $62.5 billion in 2009 to an estimated at a CAGR of 5.8% between 2009 and 2016 to reach $91.3 billion by 2016. Growth in generics and oncology market and rising focus on high potency API are driving the growth of API market. The excipient market will also show a growth rate4% between 2006-2016 to reach $536m by 2016.the trend of outsourcing of the manufacturing operation to the CMO has increased in recent years and GBI Research estimates that CMO market manufacturing of for solid dosage forms will grow at a rate of growth from $11.2 billion in 2009 to reach $24.5 billion by 2016 with a CAGR of11.8% between 2009-2016.

Scope

The scope of this report includes -

* Key emerging technologies in the manufacturing of solid dosage forms
* Market revenues and forecasts for API's, excipeints and CMO market for manufacturing of solid dosage forms.
* Qualitative analysis of the market drivers, barriers, future outlook and challenges for the API, excipient and CMO market.
* Manufacturing trends and new technologies used for manufacturing of solid dosage forms.
* Challenges and unmet needs in manufacturing of solid dosage forms.
* Regulatory aspects related to the manufacturing of solid dosage form.
* Single use technology trends, benefits, and challenges in downstream bioprocess that shape the bio manufacturing industry
* Analysis and competitive assessment of leading and evolving players involved in manufacturing of solid dosage forms.


Reasons to buy

The report will enhance your decision making capability. It will allow you to -

* Formulate strategies to increase your company's growth by understanding the new growth opportunities, market size and growth prospectus in market for manufacturing of solid dosage forms.
* Work around the technology hurdles by identifying the key trends shaping and driving the market for manufacturing of solid dosage forms.
* Device a more tailored country strategy through the understanding of key drivers and barriers to market for manufacturing of solid dosage forms.
* Differentiate yourself from competitors and develop new solutions for the manufacturing industry by understanding the existing competitive landscape and how it is evolving to meet the increasing demands.


For more information or to purchase this report, go to:
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Partial Table of Contents:

1 Table of Contents
1.1 List of Tables
1.2 List of Figures
2 Manufacturing of Solid Dosage Forms: Introduction
2.1 GBI Research Report Guidance
3 Manufacturing of Solid Dosage Forms: Overview
3.1 General Manufacturing Process for Solid Dosage Forms
3.1.1 Dispensing
3.1.2 Sizing
3.1.3 Powder Blending
3.1.4 Granulation
3.1.5 Drying
3.1.6 Tablet Compression
3.1.7 Packaging
3.2 Granulation
3.2.1 Dry Granulation
3.2.2 Wet Granulation
4 Manufacturing of Solid Dosage Forms: Market Overview
4.1 Overview of Drug Formulations Market
4.2 Solid Dosage Form Market
4.3 Drivers and Restraints in the Solid Dosage Market
4.3.1 Drivers
4.3.2 Restraints
4.4 Major Components of the Solid Dosage Forms Market
4.4.1 Active Pharmaceutical Ingredients (APIs)
4.4.2 API Drivers
4.4.3 API Market Constraints
4.4.4 Excipients
4.4.5 Excipients Drivers
4.4.6 Excipients Restraints
4.5 Outsourcing of Manufacturing
4.5.1 Global Pharmaceuticals CMO Market Overview
4.5.2 CMO Market Size for Solid Dosage Forms
4.5.3 Key Drivers
4.5.4 Key Restraints
5 Manufacturing of Solid Dosage Forms: Technology Lanscape
5.1 Manufacturing Trends Used for Solid Dosage Forms
5.2 Innovative Technologies for Solid Dosage Manufacturing
5.2.1 Fluidized Hot-Melt Granulation
5.2.2 Hot-Melt Extrusion (HME)
5.2.3 Dry Emulsions
5.2.4 Bohle Tablet Coater (BTC)
5.3 Batch versus Continuous Process
6 Manufacturing of Solid Dosage Forms: Challenges and Unmet Needs
6.1 Unmet Needs
6.1.1 Solid Dosage Products Based on High Active Compounds
6.1.2 Compliance with cGMP Guidelines
6.1.3 Redesigning Manufacturing Platforms
6.2 Challenges
6.2.1 Regulatory Hurdles for Continuous Process Facilities
6.2.2 Innovative and Efficient Excipients Required
7 Manufacturing of Solid Dosage Forms: Regulatory Landscape
7.1 cGMP Guidelines
7.2 For API cGMP Guidelines
7.3 Excipient Regulation
7.3.1 Comparison of the US, Europe and Japan
7.4 For Excipients cGMP Guidelines
7.4.1 The IPEC Excipient Guide
7.4.2 The IQA/PQG Guide
7.4.3 Application of the PQG standard
7.4.4 IPEC and PQG Standards Comparison
7.4.5 Regulatory Basis for Supplier Qualification
8 Manufacturing of Solid Dosage Forms: Competitive Landscape
8.1 Patheon

Full Table of Contents is available at:
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