Our activities include all the steps required, beginning from the development of a pharmaceutical product up to the placement of such a product on the market.
Utilization of highly qualified specialists, external academic researchers and CROs, when needed, in order to perform all the necessary studies, so as to develop the ideal product composition, as well as all the necessary processes that will be needed to produce it.
Preparation of registration dossiers according to the current legislation (e-CTD format)
and submission through national, DCP and MRP procedures.
Manufacturing facilities’ audits
Performance of GMP-compliance audits, starting with their planning, execution and
finally the audit report compilation, according to the latest European legislation.
Pharmacovigilance services according to the current legislation in Cyprus, Greece and all European countries.
Terix Labs also offers the above-mentioned services to partners interested for in-licensing the products that have been developed by the company.