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Compliance to Regulations and the PAT Initiative Remain Top Market Drivers in the European Pharmaceutical Market.


DUBLIN, Ireland -- Research and Markets (http://www.researchandmarkets.com/reports/c88688) has announced the addition of "Automation and Control Solutions in the European Pharmaceutical Market" to their offering.

The 21 CFR CFR

See: Cost and Freight
 Part 11 regulation stipulated by the Food and Drugs Administration (FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
) was introduced in 1997. Implemented across Europe through the European Medicines Agency The European Medicines Agency (EMEA) is a European agency for the evaluation of medicinal products. Until 2004, the European Medicines Agency was known as The European Agency for the Evaluation of Medicinal Products.

Roughly parallel to the U.S.
 (EMEA), this regulation requires pharmaceutical companies to increase transparency in their production processes through audit trails and access control functions. By accepting electronic records and electronic signatures as equivalent to paper-based records and handwritten hand·write  
tr.v. hand·wrote , hand·writ·ten , hand·writ·ing, hand·writes
To write by hand.



[Back-formation from handwritten.]

Adj. 1.
 signatures, the FDA paved the way for significant changes in the way that the pharmaceutical industry maintained its records and allowed the industry to leverage technology to keep pace with the fast growth of the industry. "Compliance to various regulations such as 21 CFR part 11 and Current Good Manufacturing Practices (cGMP) put forth by the FDA remains a major factor propelling growth in the automation and control solutions market," comments the analyst of this research. "At the same time, operational efficiency, in terms of bringing down production costs, reducing time to market and increasing flexibility in production, is also a strategic reason for pharmaceutical companies to invest in automation solutions."

The Process Analytical Technology Process Analytical Technology (PAT) has been defined by the United States Food and Drug Administration (FDA) as a mechanism to design, analyze, and control pharmaceutical manufacturing processes through the measurement of critical process parameters and quality attributes.  (PAT) initiative arose from a need felt by the pharmaceutical industry to lower production costs due to pricing pressures. Traditionally, a production process was followed, wherein the quality of the manufactured drug was checked at the end of the process. However, with the PAT initiative, pharmaceutical companies have been able to ensure the quality of their drugs during the production process itself, supporting reduced time to market, reduced costs and improved quality of products. These two factors are driving growth in the automation and control solutions market due to the scope they present for the use of automation systems such as electronic batch recording systems, analytical equipment as well as solutions for improving visibility through the production process.

MES (Manufacturing Execution Software) Software that provides real time access to plant activities that include equipment, labor, orders and inventory. An MES integrates the data with enterprise resource planning (ERP) systems so that management has complete control of  Poised for Significant Growth

The manufacturing execution systems (MES) segment is one of the fastest growing product segments within the automation and control solutions market. MES, which acts as a bridge between the shop-floor automation layer such as programmable logic controllers (PLCs), supervisory control and data acquisition (application) Supervisory Control and Data Acquisition - (SCADA) Systems are used in industry to monitor and control plant status and provide logging facilities. SCADA systems are highly configurable, and usually interface to the plant via PLCs.  (SCADA)/human machine interface (HMI) systems and the enterprise level solutions such as enterprise resource planning See ERP.

(application, business) Enterprise Resource Planning - (ERP) Any software system designed to support and automate the business processes of medium and large businesses.
 (ERP (Enterprise Resource Planning) An integrated information system that serves all departments within an enterprise. Evolving out of the manufacturing industry, ERP implies the use of packaged software rather than proprietary software written by or for one customer. ) systems, provides the required visibility through the pharmaceutical production process. MES's per cent share in the overall automation and control solutions in the European pharmaceutical market is expected to be in the range of 20-25 per cent in 2013.

"The speedy return on investment on such solutions is fast becoming evident to the pharmaceutical industry, resulting in a high rate of uptake of such MES solutions," notes the analyst. "Growth in the MES segment also drives growth in the base automation layer, as integrating an MES system often requires an upgrade or replacement of base layer automation solutions." A $119.9 million market in 2006, MES is expected to grow at a compound annual growth rate (CAGR CAGR

See: Compound Annual Growth Rate
) of about 15 per cent to reach approximately $320 million in 2013.

This Frost & Sullivan research service titled Automation and Control Solutions in the European Pharmaceutical Market provides an analysis of the various factors driving and restraining the market, revenue forecasts, geographic trends and competitive structure. In this research, Frost & Sullivan's expert analysts thoroughly examine the following markets: programmable logic controllers (PLC), distributed control systems (DCS), supervisory control and data acquisition (SCADA), Manufacturing Execution Systems (MES), human machine interface (HMI) and advanced process control (APC (1) (American Power Conversion Corporation, West Kingston, RI, www.apcc.com) The leading manufacturer of UPS systems and surge suppressors, founded in 1981 by Rodger Dowdell, Neil Rasmussen and Emanual Landsman, three electronic power engineers who had worked at MIT. ) in the European region.

For more information visit http://www.researchandmarkets.com/reports/c88688
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Publication:Business Wire
Article Type:Industry overview
Date:Apr 15, 2008
Words:602
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