With over 25 years of experience in pharmaceutical process and support, the Honeyman Group has been instrumental in the evolution of validating pharmaceutical and biotech equipment.
Our expertise supports our clients during the initial stages of the URS (User Requirement Specification), all the way through to IQ, OQ and PQ, as well as delivering on-going re-qualification of:
We understand that downtime and asset utilisation are very important to you, hence we pride ourselves in offering our clients:
Looking to carry out the thermal validation yourself? Why not consider the wireless data loggers from Lives International, designed to reduce time carrying out validation work, calculations and documentation substantially? Find out for yourself or contact us to discuss your requirements.
For more information on how the Honeyman Group can assist you in your qualification and validation needs, choose one of the options below or contact us to discuss your requirements.