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toggle main navigation home about services links contact us -- exceeding boundaries in quality assurance bateman quality associates ltd (bqal) offers a quality assurance consultancy and interim management service to pharmaceutical and pharmaceutical development companies. our aim is to assist companies to improve efficiency and regulatory compliance of their operational activities. our pharmaceutical expertise covers good clinical practice, good manufacturing practice, good laboratory practice and good distribution practice requirements within europe, usa, asia and africa. we understand the research and development processes involved in selection of active molecules to take forward into clinical development programmes, the subsequent small scale synthesis of active pharmaceutical ingredients (api) for use in toxicological studies and development of investigational medicinal products for clinical trials. we specialise in compliance audits of third parties involved in these activities for pharmaceutical development companies. experience gained in main-stream chemical and pharmaceutical manufacturing environments covers simple and complex processes for api manufacture (small molecules, fermentation products, biologics and vaccines) in small and large batch sizes and a wide range of finished product dosage formats including sterile products (terminal sterilisation and aseptic filling). we have experience of site and plant specific audit by european, us and asian regulatory bodies. we offer our services throughout most regions of the world. about bqal - dr tim bateman tim is a leader within pharmaceutical quality assurance (qa) with over 30 years experience in operational and corporate positions gained in both large and small companies. with a phd in microbial biochemistry from university college cardiff, tim is also a chartered chemist, a fellow of the royal society of chemistry and a member of the pharmaceutical quality group (pqg). tim has in depth knowledge of api manufacture and his background enables him to understand the often complex chemistry involved in multiple stage synthesis of a molecule and consequently how the gmp requirements need to be applied to the molecules manufacture. tim has has first hand experience of the drug development functions, including the manufacture and control of investigational medicinal products for use in clinical trials as well as primary and secondary product manufacturing (all dosage formats) for mainstream pharmaceutical manufacturing. tim is experienced in regulatory compliance requirements within europe, usa, asia & africa and has a wide range of skills including: development, maintenance and continuous improvement of quality management systems; management of qa groups; hosting successful regulatory authority inspections (fda and mhra) in support of manufacturing & marketing authorisations; management and auditing of pharmaceutical supply chain; quality management of validation systems; commissioning of manufacturing and laboratory facilities; analysis of starting materials and products; troubleshooting. dr tim j bateman bsc msc cchem frsc about bqal - karen bateman karen is a quality assurance professional with over 35 years experience gained within pharmaceutical manufacturing, pharmaceutical research & development / clinical trial environments and fertility healthcare clinics. having attained a diploma in analytical chemistry from the university of hull, karen is a chartered chemist, a fellow of the royal society of chemistry and has experience as a qualified person for investigational medicinal products. karen has practical experience of developing, maintaining and improving quality management systems to meet current regulatory and a number of iso standard requirements related to both commercial and development activities within the pharmaceutical industry. karen has first hand knowledge of the qa and supply chain management audit requirements relating to active molecule selection for clinical development programmes; the subsequent small scale api synthesis for use in toxicological studies and imp development for clinical trials. experience gained in chemical manufacturing and pharmaceutical environments covers simple and complex processes for api manufacture and a wide range of finished product dosage formats. karen can provide qa support to companies on an interim management or fee for services basis and is happy to be approached to discuss individual company requirements. karen bateman cchem frsc services qa consulting services quality management system development and review qa management responsibilities batch record review and approval risk management change control programme capa development/support vendor and supplier audit / qualification regulatiory dossier review (ind / nda / ctd) auditing services quality system evaluation audit of in-house systems for gmp / gdp / gcp and hfea / cqc regulatory requirements service provider and supply chain audits compliance gap assessments pre approval inspection support & mock regulatory audits compliance audits against ich quality and efficacy guidelines validation audits links here are some links that may be useful association of americal pharmaceutical scientists association of the british pharmaceutical industry international pharmaceutical excipients council international society for pharmaceutical engineering parenteral drug association pharmaceutical quality group european medicines agency us food and drug administration uk medicines and healthcare products regulatory agency pharmaceutical insepction co-operation scheme eudralex – rules governing medicinal products in the eu human fertilisation and embryology authority contact us your name* email address* phone your message* please leave this field empty. home about services links contact us dr tim bateman office: +44 (0) 1487 840458 m: +44 (0) 7765 935665 e: [email protected] karen bateman office: +44 (0) 1487 840458 m: +44 (0) 7495768510 e: [email protected] bqal the smiddy 2 blacksmiths end bluntisham cambridgeshire pe28 3jh © 2018 bateman quality associates limited website by b a a m

URL analysis for bqal.co.uk

http://www.bqal.co.uk/#links
http://www.bqal.co.uk/#services
http://www.bqal.co.uk/#home
http://www.bqal.co.uk/#about
http://www.bqal.co.uk/#contact
hfea.gov.uk
abpi.org.uk
mhra.gov.uk

Whois Information

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Error for "bqal.co.uk".

the WHOIS query quota for 2600:3c03:0000:0000:f03c:91ff:feae:779d has been exceeded
and will be replenished in 32 seconds

WHOIS lookup made at 05:21:29 08-Sep-2017

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  REFERRER http://www.nominet.org.uk

  REGISTRAR Nominet UK

SERVERS

  SERVER co.uk.whois-servers.net

  ARGS bqal.co.uk

  PORT 43

  TYPE domain

DISCLAIMER
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:
Copyright Nominet UK 1996 - 2017.
You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at http://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REGISTERED no

DOMAIN

  NAME bqal.co.uk

NSERVER

  NS3.LIVEDNS.CO.UK 213.171.192.254

  NS2.LIVEDNS.CO.UK 213.171.193.250

  NS1.LIVEDNS.CO.UK 213.171.192.250

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