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CPhI Report Warns Industry Must Actively Drive Process Improvements Itself to Meet Growing Global Demand


News provided by

UBM Live

Apr 24, 2014, 07:57 ET

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AMSTERDAM, April 24, 2014 /PRNewswire/ --

Improved process efficiency, with modern manufacturing techniques could save billions and increase profits, improve quality and open up sales in developing markets 

UBM Live Logo (PRNewsFoto/)
UBM Live Logo (PRNewsFoto/)

Girish Malhotra, CPhI expert panel view: "'Process centricity' has to overtake the current 'regulation centricity' if pharma wants to see cost reductions in new and existing processes."

     (Logo: http://photos.prnewswire.com/prnh/20130723/629764-a )

Report highlights: 

  • Manufacturing efficiencies must be driven by big pharma, not regulators as this will only increase costs
  • 'Improving product quality' and 'reducing manufacturing costs' are the industry's major priorities
  • 70% investing in manufacturing this year, with 59% also hiring more staff
  • 59% are increasing the use of outsourcing
  • Nearly 50% of the industry stated they introduced more than three products last year, with a further 41% adding 1-3 products
  • 'Improved efficiency' and 'improved safety' were highlighted as the most important manufacturing goals

CPhI Worldwide, part of UBM Live's Pharmaceutical Portfolio, announce the findings of its Pharma Insights report on Manufacturing. Overall the report indicates that the industry is aware of the need to continue to improve manufacturing practices, processes and efficiencies to dive down costs and improve profits and drug quality. However, the report warns that industry must more actively take the lead if we are to see these vital changes driven through- currently, the inertia of the existing model is impeding innovation and preventing wide spread adoption.

CPhI adds that most of the sector now states it is utilising continuous process improvements to drive efficiency savings, but more could be done to revolutionise practices. CPhI findings show that 26% are using 'statistical process control', 21% using 'process capability analysis', 16% QbD, 12% 'six sigma' and 11% using both 'lean/kaizen' and 'PAT'. Furthermore, many are building for the future and making essential upgrades to existing equipment with 70% actively investing in manufacturing.

In the medium to long term, we should see a cross-pollination of process improvements from generics (where costs savings can still be made) though CMOs and ultimately into big pharma's patented products. The advantage here is that lower cost patented products would open huge new markets, whilst reducing the attractiveness of counterfeits.

For cost savings to be made however, the report clearly states further improvements must come from the industry itself and not the regulator, as this will only increase costs.

CPhI panel member and President of EPCOT International Girish Malhotra, added: "Not much will change in the current processes as the needed regulatory approval will come in the way of any improvement of existing processes. Success to exceed regulations will only come from process inception stage along with command of the process as they become commercial. 'Process centricity' has to overtake the current 'regulation centricity' if pharma wants to see cost reductions in new and existing processes."

In terms of the industry's economic strength, the findings show the sector is in good health with 59% planning to increase headcount this year and only 4% planning reductions. In outsourcing we continue to see increases with 41% outsourcing more of their manufacturing. Going forwards, if manufacturers want to improve product quality, they must find a supplier that aligns with their own GMP compliance expectation.

Additionally, nearly 50% of the industry stated they introduced more than three products last year, with a further 41% adding 1-3 products.

The biggest manufacturing goals are to 'increase efficiencies' and 'safety' and already 89% are testing raw material sourced- with 'compendial testing' by far the most favoured method (81%).

"With the majority of the industry now committed to process improvements and increased product quality the next few years will hopefully see more new manufacturing methods coming to market, with tighter process controls - these should ultimately reduce costs and increase profits for the industry." Chris Kilbee, Group Director Pharma.

CPhI believes we may be at the cusp of a revolution and if one major pharma company starts reaping the benefits of implementing process perfection from initial development to commercialisation others will follow. Drawing all these findings together the report concludes that the industry has made great strides and with new efficient techniques drugs should be more available globally at reduced cost, enabling developing countries increased access.

Chris Kilbee added: "The desire to modernise processes across the industry is clearly there and taking a long term view we can see that the way we conduct development work right through to commercialisation has the chance to revolutionise the business model. Patented products will be opened up to a wider number of the globe's seven billion inhabitants, which is a real human goal, but also one that will see the industry become more sustainable and increase profits. I believe that with these commitments we see a situation where industry actively drives improvements and takes these new methods to the regulator- cost savings and improved quality should go hand in hand".

Full report: http://www.cphi.com/documents/129623/1317492/CPhI+Pharma+Insights+Report-+Manufacturing.pdf/2fe19c18-9641-4a60-9846-4fbb561cb8a6 

About CPhI 

CPhI drives growth and innovation at every step of the global pharmaceutical supply chain from drug discovery to finished dosage. Through exhibitions, conferences and online communities, CPhI brings together more than 100,000 pharmaceutical professionals each year to network, identify business opportunities and expand the global market. CPhI hosts events in Europe, China, India, Japan, Korea, Southeast Asia, Istanbul, Russia and South America and co-locates with ICSE for contract services, P-MEC for machinery, equipment & technology, InnoPack for pharmaceutical packaging and BioPh for biopharma. CPhI provides an online buyer & supplier directory at CPhI-Online.com.

For more information visit: http://www.cphi.com

The UBM Live annual schedule of Pharmaceutical events also includes CPhI Russia and IPhEB (16-17 April, 2014 at the Lenexpo Exhibition Complex- St Petersburg, Russia); CPhI, P-MEC and Innopack South East Asia (20-22 May, 2014 at the Jakarta International Expo- Jakarta, Indonesia); CPhI Istanbul (4-6 June, 2014, at the Lutfi Kirdar Convention and Exhibition Centre- Turkey); CPhI, Hi and Fi, ICSE, P-MEC, BioPh and LabWorld China (26-28 June, 2014 at SNIEC- Shanghai, China); CPhI South America (5-7 August 2014 at Expo Centre Norte, Sao Paulo- Brazil); CPhI, ICSE Korea (2-3 September, 2014 at the COEX- Seoul, South Korea); CPhI, ICSE, P-MEC and InnoPack Worldwide (7-9 October 2014, Paris Nord Villepinte- France); CPhI and P-MEC India (2-4 December, 2014 at the Bombay Exhibition Centre- Mumbai); CPhI, ICSE, P-MEC, BioPh and Pharmatec Japan (22-24 April, 2015 at the Big Sight Exhibition Centre- Tokyo).

About UBM Live 

UBM Live connects people and creates opportunities for companies across five continents to develop new business, meet customers, launch new products, promote their brands, and expand their market. Through premier brands such as TFM&A, Internet World, IFSEC, MD&M, CPhI, Cruise Shipping Miami, the Concrete Show, and many others, UBM Live exhibitions, conferences, awards programs, publications, Websites, and training and certification programs are an integral part of the marketing plans of companies across more than 20 industry sectors.

For media enquiries, please contact:

Alex Heeley or Tristan Jervis    
De Facto Communications
T: +44-207-203-6745 / 6740
E: [email protected] / [email protected]

SOURCE UBM Live

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