UK company providing regulatory pharmaceutical and medical devices validation and quality compliance services offers subcontracting services
This UK company has over 25 years worldwide consultancy experience in the pharmaceutical and medical devices industry. Areas of expertise are pharmaceutical validation, compliance, audit, quality assurance and system development as well as project rescue, training and person-in-plant. The company offers their services on a sub-contracting basis for short or long term contracts throughout the world.
This company has over two decades of experience working with some of the world’s largest pharmaceutical and medical device manufacturers. They have worked with numerous overseas clients on a variety of long and short term contracts providing cost effective consultancy advice on Medicines and Healthcare Products Regulatory Agency (MHRA) and Food and Drug Administration Agency (FDA) regulations.
Over the last 25 years, this UK based company has worked with some of the world’s leading pharmaceutical manufacturers, active pharmaceutical ingredient manufacturers and medical device manufacturers and are experts in areas of quality assurance and validation. This includes provision of: • audit services • assessments • advice on preparing for regulatory audits by the Medicines and Healthcare Products Regulatory Agency (MHRA) and Food and Drug Administration Agency (FDA) • assistance with quality system design • corrective and preventive action (CAPA) and deviation close out • response to inspection findings • audit training • person-in-plant • project rescue • technical proof reading The company is hoping to extend their network of clients throughout the world by offering its services on a sub-contract basis, and can be called on for both short and long term contracts.
06001013Medical Technology / Biomedical Engineering
06001015Pharmaceutical Products / Drugs
05007007Other medical/health related (not elsewhere classified)
M.74.9.0Other professional, scientific and technical activities n.e.c.
Q.86.9.0Other human health activities
Organisations wishing to use this UK company as a subcontractor could be innovative pharmaceutical manufacturers, active pharmaceutical ingredient manufacturers or medical device manufacturers. They could be seeking to establish quality compliance procedures in preparation for regulatory compliance audit or seeking to increase operational efficiencies to maximise production capacities.
SME 11-50,251-500,SME 51-250,>500
Already on the market
Industry SME <= 10
With over 25 years experience working with some of the largest companies in the pharmaceutical industry this UK company has built up a reputation for a quality cost efficient service.