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Found articles: 10

  • Mini Moto Tips
    These are some quick adjustments and tips for the B1 liquid cooled minimoto that I have found helpful.Extra heat protection:To protect the bike I've put some aluminium tape on the inside of the fairing at the closest point to the exhaust and on the underside of the fuel tank. I?More

  • Know Your Mini Moto
    The Mini Moto is a small scale replica of the World Super Bikes used by the likes of Valentino Rossi and ex champion Carl Fogarty. The Mini Moto comes equipped with either a two stroke air or water cooled engine which are, depending on the model, capable of speeds of up to 60Mph.In this article I will underline the finer points of the components that make these speeds possible.More

  • How to Remove Your Mk2 Mini Moto Engine
    Many mini moto modifications will require you to remove the engine from the mini moto. This is why I have produced the following guide.Firstly you will need to remove the mini moto’s fairing.More

  • Mini Moto Mayhem
    Mini Motos have been around in the UK for around ten years now. The first bikes we’re cobbled together with parts that were already available. Small 2 stroke engines, mainly from garden machinery, were used.More

  • Mini Moto Engine
    Industrial engines. They are still used by several manufacturers (most notably Blata on their entry level bike) and typically produce between 2.5 and 3.More

  • How to Become a Qualified Person Consultant
    If you are a Qualified Person with a full time position. You may be interested to know that there are many organizations that require the skills and expertise of a Qualified Person consultant.The organisation may require periodic batch release and would only require a QP at these times.More

  • The Advantages of Consultative Qualified Person Services
    The concept of the Qualified Person is exclusive to the European Union and was first established 1975.According to EU directives pharmaceutical companies must employ the services of a MHRA/VMD accredited Qualified Person (QP) to adhere to the following applicable regulatory requirements. Good Manufacturing Practice (GMP) for medical products (2003/94/EC) Good Manufacturing Practice (GMP) for veterinary medicinal products (91/412/EEC) Good Clinical Practice (GCP) in conduct of clinical trials (2001/20/EC) Community code relating to veterinary medicinal products (2001/82/EC) Community code relating to medicinal products for human use (2001/83/EC)Companies that manufacture medicines and drugs for clinical trials can often find that increases in demand, new ventures or unexpected changes in personnel require the services of a contract consultant QP.More

  • The Business Advantages of Conference Calling Using the Internet
    The Internet provides a practical venue for the conference call. With its low cost and ability to accomodate many listeners it is now practical to open a conference call to almost anyone (at least to listen). Many firms now do.More

  • Can England Win the 2006 World Cup in Germany?
    Beckham first captained England in a friendly against Italy. Since then he has continued to lead by example with a terrific work ethic. This has never been more apparent than in the deciding world cup qualifier against Greece.More

  • Routine Duties of a Qualified Person
    Qualified Persons are required to perform routine duties in line with the general principals of a QP. A Qualified Person must ensure that the following criteria is completed before batch release is possible:The batch must meet ‘The Marketing and Manufacturing Authorisation or Investigational Medicinal Products Authorisation requirements for Medical Products.The GMP guidelines as stated in Directive 2003/94/EC (human) or Directive 91/412/EEC (veterinary).More