Attachment
3rd Annual Contract Manufacturing in Pharma & Biotech
Achieving success through an integrated approach in strategic outsourcing
To be held at 16th – 18th November 2009, BSG Conference Centre, London, UK
Background Info.
The biggest driver for outsourcing to the CMOs is the availability of exclusive, novel and innovative production technology that they offer to pharma and biotech companies. Many CMOs have improved themselves beyond the immediate needs of their customers. By creating innovative processes that often surpass the in-house technology available at major pharma and biotech companies.
3rd Annual Contract Manufacturfing fin Pharma & Bfiotech conference examine the current and emerging trends, that are mobilising contract manufacturing companies, and shifting the focus from the west to east. This conference will address various quality, regulatory and development challenges to establish cost-effective and successful outsourcing alliances.
As the global outsourcing landscape is changing, this conference will unleash opportunities to sustain a robust growth in the current economy.
By attending this conference you will gain knowledge on:
• How the globalisation of the contract manufacturing market is shifting focus from the west to east
• Outsourced laboratory compliance and qualifi cation services
• Using PAT to accomplish real time release/continuous manufacturing
• New shifts: from API to FDF, from generic drugs to R&D based companies
• How to think globally and outsource locally
• CMO’s and SME’s: the route to success of a virtual specialty pharmaceutical company
• Designing major pharmaceutical drug dosage forms
• Biostorage – A critical and strategic component of the worldwide drug development process
• Outsourcing APIs to India: a cheaper way
• Screening process to identify a suitable outsourcing partner
• Embracing Quality by Design (QbD)
• How to administer packaging engineering and design
Target Audience
Pharmaceutical and Biotechnological Companies
Contract Manufacturing Organisations (CMOs)
Drug Regulators, Intellectual Property/Law Firms
Academia, Government Bodies, Regulatory Affairs
Who should attend?
VP, Directors, Managers, Team Leaders, Senior Scientists, in:
CMC
• R & D
• Biologics
• API and Technical Development
• Formulations Development
• Drug Dosage Form
• QbD/PAT
• Pharmaceutical Science & Process
Development
• Bioprocess Research
• Manufacturing Science and
Technology
• Contract Management
• Contracts & Outsourcing
• Operations
• Strategic Alliances
• Planning & Logistics
• Procurement & Purchasing
• Business Process Excellence
• Sales & Marketing
• Regulatory Affairs / Compliance
• Quality Assurance
For more kindly visit : http://www.bharatbook.com/
OR Contact us at
Bharat Book Bureau
207, Hermes Atrium, Sector 11, PO Box.54, CBD Belapur, Navi Mumbai - 400 614, India.
Phone : +91 22 2757 8668 / 2757 9438
Fax : +91 22 2757 9131
E-mail : info@bharatbook.com
Website : www.bharatbook.com
