We know that every project is unique and hence we provide our clients with a dedicated project manager who focus on a proactive team approach for the management of your clinical service needs.
Our clinical project team have extensive experiences gained within the pharmaceutical industry and we can manufacture clinical trial material for all stages of clinical development.
At Rechon we have the capacity to manufacture and package for clinical trial use, providing a full range of services that include the manufacture and blinding of actives, placebos, and comparators including controlled drug products. We can source comparator material to meet almost any study requirements.
Our services include:
– Clinical manufacturing, phase I, II, III and IV
– Import of clinical trial supplies
– Labelling, packaging, blinding and distribution to clinical sites worldwide
– QP and regulatory release
– Regulatory support documentation (CMC/Module 3)
– IND and IMPD documentation
We can manage the entire clinical supply chain from manufacturing through transport to clinics, returns and destruction.
If you are interested in clinical services, please contact us for more information or a quotation for your specific project.
Roland Holmqvist, CEO +46 709 482424
Maria Wingren, Project Manager +46 733 999202
Elisabet Lindh-Elliot, Clinical Development Manager +46 732 751346
Rechon is a manufacturer of aseptic vials, ampoules, syringes, oral and nasal sprays from small quantities for clinical trials up to full-scale commercial supply for worldwide markets. Our facility operates under cGMP and we are regularly inspected by the Swedish Medical Products Agency, US FDA and other Health Authorities.