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RBBBD
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MENA Regulatory Conference on Bioequivalence,. Biowaivers, BIOANALYSIS, DISSOLUTION AND BIOSIMILARS. Jordan September 15-17, 2015. Following the remarkable success of the 1st MENA Regulatory Conference on Bioequivalence, Biowaivers, Bioanalysis and Dissolution , held in Amman in 2013, with more than 300 participants; the AAPS, FIP, TUFTAD and IPRC are organizing the 2ed MENA Regulatory Conference on Bioequivalence, Biowaivers, Bioanalysis, Dissolution and Biosimilars in Amman, September 15th to 17th, 2015.
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Regulatory Activities | Kennet Bioservices Ltd
http://www.kennetbioservices.com/regulatory-activities
Skip to Main Content. Your global bioservices specialists. Preparation of dossiers for submission for marketing authorisations. Quality Overall Summaries, Licence variation, Centralised Technical Document (CTD) in e-format, Self Inspection/internal audit schedule preparation. Support and guidance for European (MHRA) Inspections, USFDA Inspections, GCC (Gulf States), TGA (Australia), MCC (South Africa). QP: Qualified Persons Services. 6 Kingsdown Orchard, Swindon, Wiltshire, SN2 7RR, UK.
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Our Partners | Kennet Bioservices Ltd
http://www.kennetbioservices.com/our-partners
Skip to Main Content. Your global bioservices specialists. Kennet Bioservices Ltd has strategic partnerships with a number of companies. Through these partnerships KBL can offer services covering the entire field of pharmaceutical activities. For each project the most suitable team of experts is assembled and managed by a Project Leader. The project leader provides a single point of contact and is responsible for the quality and efficiency of communications and progress in the execution of the project.
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Process Validation | Kennet Bioservices Ltd
http://www.kennetbioservices.com/process-validation
Skip to Main Content. Your global bioservices specialists. There are three types of Process Validation. Prospective Validation: This should be completed prior to the distribution and sale of the medicinal product. Concurrent Validation: This may be carried out in exceptional circumstances where it is not possible to carry out prospective validation. For this we would validate the process during routine production. For an example of our work click here. 6 Kingsdown Orchard, Swindon, Wiltshire, SN2 7RR, UK.
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Document Systems | Kennet Bioservices Ltd
http://www.kennetbioservices.com/document-systems
Skip to Main Content. Your global bioservices specialists. Documentation Systems can be reviewed for GMP compliance or we can provide new individual documents or documentation systems. Implementation and integration of “off the shelf” documentation systems can be carried out. Modules of documents for process validation and cleaning validation, as well as batch manufacturing documents are available either as complete “ready to use” documents or in template format for client adaptation.
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Location | Kennet Bioservices Ltd
http://www.kennetbioservices.com/location
Skip to Main Content. Your global bioservices specialists. Javascript is required to view this map. 6 Kingsdown Orchard, Swindon, Wiltshire, SN2 7RR, UK. 6 Kingsdown Orchard, Swindon, Wiltshire, SN2 7RR, UK. 01793 831595 info@kennetbioservices.com. 2010 Kennet Bioservices Ltd.
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Our Global Customers | Kennet Bioservices Ltd
http://www.kennetbioservices.com/our-global-customers
Skip to Main Content. Your global bioservices specialists. Our work takes us all over the globe so far we have worked in:. France, Germany, Italy, Spain, Ireland, UK, Norway, Denmark, Hungary, Poland, Sweden, Holland, Switzerland, Greece, Czech Republic, Serbia, Montenegro, Macedonia, Croatia, Russia, Israel, Turkey. Lebanon, Hong Kong, Bangladesh, Yemen, India, Dubai, Singapore, Malaysia, Ras al Khaimah. Central and South America. Mexico, Brazil, Argentina. Australia, New Zealand, Japan.
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Manufacturing Reviews | Kennet Bioservices Ltd
http://www.kennetbioservices.com/manufacturing-reviews
Skip to Main Content. Your global bioservices specialists. Reviews of current manufacturing activities can be made to provide indications for process efficiency improvement and to ensure compliance with relevant GMPs. Recommendations for sourcing equipment, both for laboratories and production and APIs can be made for all aspects of manufacturing and quality control. Manufacturing reviews can be made as part of a GMP compliance audit where corrective and preventative actions (CAPA) can be identified.
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Our Services | Kennet Bioservices Ltd
http://www.kennetbioservices.com/our-services
Skip to Main Content. Your global bioservices specialists. Offers a wide range of high quality services at sensible economic prices. We have been involved in Facility Conceptual Design, through Construction Management and IQ, OQ and PQ activities. Our experts have assisted clients with both manufacturing and quality control equipment selection and have worked with clients through cleaning validation activities. 6 Kingsdown Orchard, Swindon, Wiltshire, SN2 7RR, UK. 2010 Kennet Bioservices Ltd.
