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The Consultancy Services of Telstar supports companies in the Life Sciences field (pharmaceutics, fine chemicals, health products, food supplements, cosmetics, medicinal plants, personal hygiene products and biocides) to help them comply with quality standards in force in the R&D area, Clinical Trials, Registration, and Industrial and Pharmacovigilance throughout the products' life cycle.

Telstar has highly experienced consultants who have developed their expertise in a variety of departments such as production, quality, engineering, research, and registration in Life Science industries.

Telstar offers the following services: Conceptual design of new industrial facilities, qualification (installations, HVAC, water, gas, production and analytical equipment), consultancy for compliance with GXP and ISO standards, consultancy for the registration of new products and the approval of variations, preparing registration documents (DMFs and CEPs), preparing the Site Master File, auditing of compliance with GMP/ISO standards, readability tests of patient information leaflets, consultancy for validation (computer systems, cleaning, manufacturing processes and analytical methods), evaluation of registration dossiers, Due Diligence participation, quality consultancy for Preclinical and Clinical Research, implementation of Pharmacovigilance systems,  GMP/GLP/ISO training, implementation of Risk Analysis and Ongoing Improvement projects, galenical development studies, development of analytical methods and stability studies, business development (purchase/sale of licenses, manufacturer search, technology transfer).