AlthoTech Consulting Inc. Pharmaceutical and Biotechnology Clinical Consulting
Email: consulting@althotech.com;     Tel: 647 515 5314


CMC Management  •  QP Services  •  Clinical Packaging  • Regulatory Submissions


Welcome


AlthoTech Consulting Inc. (AlthoTech) is a Toronto based, world-wide consulting company that specializes in supporting North American pharmaceutical and biotechnology companies in progressing new products into early clinical trials.


AlthoTech supplies two types of services for clinical development projects:


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AlthoTech’s expertise is the Chemistry Manufacturing Control (CMC) aspects of new product development.  AlthoTech assumes responsibility for executing all GMP activities necessary to initiate clinical trials following the declaration of a product candidate by a Client.  AlthoTech also specializes in clinical packaging and clinical regulatory filings on a world-wide basis.


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In addition, AlthoTech has a North American based Qualified Person (QP) under EC regulations (Directive 2001/83/EC), and included on the Royal Society of Chemistry (UK) list of QPs.  As a QP, AlthoTech understands the legislation and pharmaceutical issues around importing investigational medicinal products into Europe .


AlthoTech offers QP services in two areas: